Abstract
Organ function declines with age, and large-scale transcriptomic analyses have highlighted differential aging trajectories across tissues. The mechanisms underlying shared and organ-selective functional changes across the lifespan, however, still remains poorly understood. Given the central role of mitochondria in powering cellular processes needed to maintain tissue health, we therefore undertook a systematic assessment of respiratory activity across 33 different tissues in young (2.5 months) and old (20 months) mice of both sexes. Our high-resolution mitochondrial respiration atlas reveals: 1) within any group of mice, mitochondrial activity varies widely across tissues, with the highest values consistently seen in heart, brown fat, and kidney; 2) biological sex is a significant but minor contributor to mitochondrial respiration, and its contributions are tissue-specific, with major differences seen in the pancreas, stomach, and white adipose tissue; 3) age is a dominant factor affecting mitochondrial activity, especially across different fat depots and skeletal muscle groups, and most brain regions; 4) age-effects can be sex- and tissue-specific, with some of the largest effects seen in pancreas, heart, adipose tissue, and skeletal muscle; and 5) while aging alters the functional trajectories of mitochondria in a majority of tissues, some are remarkably resilient to age-induced changes. Altogether, our data provide the most comprehensive compendium of mitochondrial respiration and illuminate functional signatures of aging across diverse tissues and organ systems.
eLife assessment
The authors present an important resource to quantify mitochondrial function across many organs in mice. The convincing conclusions are supported by the identification of processes that specifically differ between young and old, or between male and female mice. All reviewers point to the merit of this study in providing a comprehensive resource to contextualize mitochondrial functions across the body. Some further suggestions are made to clarify conclusions in terms of data normalization, interpretations of comparative analyses between organs.
Introduction
Aging is complex biological phenomenon that results in functional decline across tissues and organs systems (1). Age is one of the most significant contributors to disease risk (2), and the aging process is influenced by a variety of genetic and environmental factors at the tissue and organismal level (3–5). The application of omics technologies in recent years has led to unprecedented insights into the complex biology of aging (6). Bulk and single-cell transcriptomic analyses of mouse tissues across the lifespan have shown that aging tempo and trajectory, as indicated by tissue transcriptomic signatures, varies widely across tissues (7–9). Remarkably, many of the transcriptomic signatures of aging across tissues can be significantly reversed by caloric restriction or rejuvenated by the transfusion of young blood (10, 11). Large-scale proteomics analyses of the human plasma proteome also reveal distinct waves of changes across the lifespan, which are associated with distinct biological pathways and affect age-related phenotypic traits and diseases (12, 13).
Despite enormous progress, there is no consensus regarding the mechanisms underlying aging at the cellular and tissue level. Although many non-mutually exclusive hypotheses have been put forth to explain the root cause of aging—oxidative damage, genomic instability, epigenetic changes, loss of proteostasis, mitochondrial dysfunction, DNA damage, telomere shortening, cellular senescence, stem cell exhaustion—it remains a major challenge to distinguish between the driver and passenger mechanisms of aging (14). Nevertheless, efforts to understand the proximal and ultimate cause of aging will facilitate development of therapeutics aimed at improving healthy aging (15, 16).
In the present study, we focused on aging from a mitochondrial perspective, as this organelle is known to play an important role in the aging process (17–20). Mitochondria supply the bulk of the energy needed to maintain tissue health and repair tissue damage, and their function tends to decline with age. Over time, damage accumulates in mitochondrial DNA, proteins, and lipids, which compromises their functional integrity and leads to dysregulated metabolism and increased oxidative stress. Recent transcriptomic analyses have highlighted major reductions in electron transport chain genes across the lifespan (7), and these changes can be significantly reversed by the transfusion of young blood into an old mouse (10).
Aging-associated reduction in mitochondrial OXPHOS genes appear to be conserved between human, mouse, fly, and worm (21). Accordingly, mitochondrial dysfunction has been implicated in various age-related diseases, including neurodegenerative disorders, cardiovascular diseases, and metabolic syndromes (22). Boosting mitochondrial health has been shown to delay age-related decline in organ function (23–26).
Given the central role of mitochondria in tissue health, we aimed to address the extent and magnitude of aging-induced changes in mitochondrial function across tissues and organ systems. Although many studies have examined mitochondrial respiratory capacity in various tissues, the scale was limited in that only a very small number of tissues could be interrogated at the same time. This is largely due to the inherent low-throughput method of assessing respiration which requires freshly isolated mitochondria or cells from tissues (27). Consequently, it was not previously feasible to have a comprehensive and systems-level analysis of mitochondrial function across many tissues and the lifespan.
This barrier, however, has been recently overcome. An innovative method by Acin-Perez and coworkers has made it possible now to assess mitochondrial function in previously frozen tissues (28). This new method circumvents the requirement for the isolation of mitochondria at the time of tissue harvest, allowing a large number of tissues (e..g., from a mouse) to be collected, frozen, and assayed at a later time. We adopted the new method in a standardized workflow to profile mitochondrial activity in 33 tissues from young and old mice of both sexes. The dataset consists of a total of 1320 tissue samples from 40 mice and 3960 high-resolution respirometry assays encompassing three technical replicates. Our study represents the largest and the most comprehensive tissue respirometry analysis to date. Our data provide an unprecedented view on the variations and changes in mitochondrial functional capacity across tissues, sex, and age, thus informing ongoing studies on the causes and consequences of aging.
Results
Pan-tissue mitochondrial respiration atlas overview, work-flow, and analysis pipeline
To assay mitochondrial respiration and its maintenance across age and sex, we collected 33 tissues from young (2.5 months; ∼18-year-equivalent in human) or old (20 months; ∼65-year-equivalent in human) male or female mice (n = 10 mice per age and sex). The tissues collected include different brain regions (hippocampus, cortex, cerebellum, and hypothalamus), different sections of the GI tract (stomach, duodenum, ileum, jejunum, cecum, proximal colon, and distal colon), various fat depots (gonadal, inguinal, mesenteric), different skeletal muscle groups (tongue, diaphragm, quadriceps complex, hamstrings, gastrocnemius, plantaris, and soleus), reproductive organs (testis and fallopian tubes), as well as liver, pancreas, heart atria and ventricle, spleen, kidney cortex and medulla, eye, and skin (Figure 1A). Our aim was to provide a comprehensive systems-level view of mitochondrial respiration across tissues, sex, and age.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_fig1.tif/full/max/0/default.jpg)
Pan-tissue mitochondrial respiration atlas overview, work-flow, and analysis pipeline.
A. Study overview highlighting the 33 different tissues collected from four different groups of mice (n = 10 / group) for respirometry analysis and mitochondrial content quantification. The four groups of mice are young male, young female, old male, and old female. Young = 10-week-old; old = 80-week-old. B. General schematic showing the preparation of samples for respirometry analysis. C. General representation of the electron transport chain to illustrate the key components of the respirometry assay used to assess mitochondrial function, the associated data, and examples of subsequent data analysis. AA, Antimycin A; Rot, Rotenone; TMPD, N, N, N’, N’-tetramethyl-p-phenylenediamine; Asc, Ascorbate; NADH, nicotinamide adenine dinucleotide.
Our standardized workflow involved thawing frozen tissue samples in buffer, minced, and homogenized. Samples were centrifuged to pellet cell debris and the supernatant was collected for immediate protein and mitochondrial content quantification (via MitoTracker Deep Red, MTDR). Sample respiration rates were then assayed using a Seahorse XFe96 Analyzer (Figure 1B). The basic respiration assay consisted of four sequential steps: first, baseline unstimulated measurements were obtained. Then, NADH was used to assess respiration via mitochondrial complex I (CI), or succinate was used as to assess respiration via mitochondrial complex II (CII) in the presence of rotenone (Rot, a CI inhibitor). Following this, samples were exposed to rotenone and antimycin A (AA, a complex III inhibitor) to silence respiration. Then, TMPD in the presence of ascorbate was used to assess respiration through mitochondrial complex IV (CIV), via donation of electrons to cytochrome c (Figure 1C). Detailed information of the methodology can be found in the methods section, which closely follows the method first described by Acin-Perez et al (28). High resolution respirometry data for each of the 33 tissues were used in all subsequent comparison (Figure 1-figure supplement 1-33).
Mitochondrial function across different organ systems in male and female mice
The first analysis made was within a group (male, female, young, or old) across all tissues. This allowed us to focus on shared and unique mitochondrial properties across different tissues within a single mouse system. Ranking young male or young female tissues by their respiration via CI (NADH-stimulated), CII (succinate-stimulated), or CIV (TMPD and ascorbate-stimulated) showed that both sexes have the greatest oxygen consumption in the heart atria and ventricles, brown adipose tissue (BAT), kidney cortex and medulla, and the lowest respiration in the colon (distal or proximal), plantaris muscle, jejunum, ileum, and mesenteric white adipose tissue (mesWAT) (Figure 2A-B).
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Tissue-by-tissue analysis of mitochondrial function in male and female mice.
A. Young male mitochondrial respiration through complex I (CI, NADH-stimulated), complex II (CII, Succinate stimulated in the presence of Rotenone, a CI inhibitor), and at complex IV (CIV, via TMPD + Ascorbate). B. Young (10 weeks) female mitochondrial respiration through CI, CII, and at CIV. C. Old (80 weeks) male mitochondrial respiration through CI, CII, and at CIV. D. Old (80 weeks) female respiration through CI, CII, and at CIV, respectively. n = 10 mice per tissue. All data is represented as the mean alone and organized highest (left) to lowest (right). BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; Vent, ventricles.
Ranking old male tissues by their respiration via CI, CII, or CIV showed that the heart atria and ventricles, BAT, kidney cortex and medulla have the highest oxygen consumption, while the ileum, pancreas, skin, duodenum, stomach, gonadal white adipose tissue (gWAT), mesWAT, and inguinal white adipose tissue (iWAT) have the lowest (Figure 2C). Ranking all old female tissues by their respiration via CI, CII, or CIV showed that the heart atria and ventricles, BAT, quadriceps muscles, and diaphragm have the highest respiration, while the pancreas, iWAT, mesWAT, ileum, distal colon, eyes, and skin have the lowest (Figure 2D).
Our analyses revealed a wide range in mitochondrial respiratory capacity across nearly all tissues. We observed tissue-types of high similarity, such as the different regions of the brain (Figure 2-figure supplement 1) and kidney cortex and medulla (Figure 2-figure supplement 2), as well as those displaying degrees of functional heterogeneity, such as the heart atria and ventricle (Figure 2-figure supplement 3), different skeletal muscle groups (Figure 2-figure supplement 4) and white adipose tissue depots (Figure 2-figure supplement 5), and different sections of the gastrointestinal tract (Figure 2-figure supplement 6). Together, these data help illustrate the heterogeneity or lack thereof in mitochondrial function across different tissues and organ systems. Remarkably, even when age and sex are controlled for, mitochondria within a single tissue-classification or organ system can have distinct respiration signatures.
Sex differences in mitochondrial function in young mice
The first pan-tissue comparison of mitochondrial function across groups was made between young male and female mice. In this comparison, we focused on the effects of sex on mitochondrial respiration in young mice. A systems-level view of mitochondrial respiration via CI, CII, or CIV across 32 tissues (omitting reproductive tissues) showed that young male and female mice have similar distributions in oxygen consumption rate (OCR; Figure 3A-C, left panel). Individual tissue-level analysis of respiration through CI showed no significant difference between young male and female mice (Figure 3A, right panel). However, individual tissue comparisons of respiration through CII showed that young males have higher mitochondrial respiration in the stomach and gastrocnemius muscles, and reduced mitochondrial activity in gWAT, duodenum, ileum, and distal colon, relative to young females (Figure 3B, right panel). Respiration at CIV showed that young males have higher mitochondrial activity in the BAT, kidney medulla, hippocampus, and stomach, and reduced mitochondrial activity in the gWAT, duodenum, and distal colon, when compared to young females (Figure 3C, right panel). A relative and global view of the sex-specific differences across young male and female mice showed that males have higher mitochondrial respiration in the stomach, kidney, and skeletal muscle, whereas females have higher mitochondrial respiration in the gastrointestinal tract and different fat depots (gWAT, and mesWAT (Figure 3D).
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Tissue-by-tissue analysis of young male and female mitochondrial function.
A. (left) Systems-level view of mitochondrial respiration (NADH-stimulated) through complex I (CI). (right) Mitochondrial respiration through CI across all young tissues. B. (left) Systems-level view of mitochondrial respiration through complex II (CII, Succinate-stimulated in the presence of rotenone to inhibit CI). (right) Mitochondrial respiration through CII across all tissues. C. (left) Systems-level view of mitochondrial respiration at complex IV (CIV) in the presence of rotenone and antimycin A to inhibit CI and CIII, respectively. (right) Mitochondrial respiration at CIV across all tissues. All data is presented as the mean with standard error, and organized highest to lowest for young male values. D. Heat map view of mitochondrial function across all tissues assayed (omitting reproductive organs). Data is represented as young male/female. Tissues with elevated respiration in males appear red while the same for females appear blue. Data is organized highest to lowest by summation of young male CI, CII, and CIV respiration values. n = 10 young male (YM, 10 weeks) and 10 young female (YF, 10 weeks) per tissue assayed. Statistical significance is represented as: a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001. BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; Vent, ventricles.
Effects of age on male mitochondrial function
The second tissue-by-tissue comparison of mitochondrial function was made across age, where we focused on the effects of age on mitochondrial respiration in young and old male mice. A systems-level view of respiration via CI, CII, or CIV across all 33 tissues showed that old and young male mice have similar distributions of OCR (Figure 4A-C, left panel). However, an individual tissue view showed many differences in response to age. Old males showed a striking increase in mitochondrial activity via CI in the heart atria and ventricles, skeletal muscles (quadriceps, diaphragm, soleus, tongue, plantaris), and mesWAT, and reduced mitochondrial respiration in the brain cortex, relative to young males (Figure 4A, right panel). Viewing respiration through CII also showed that old males have markedly higher mitochondrial activity in the heart, skeletal muscles (quadriceps, diaphragm, plantaris), jejunum, ileum, and mesWAT when compared to young males (Figure 4B, right panel). In contrast, old males had reduced mitochondrial activity via CII in the brain (cerebellum, cortex, hippocampus), BAT, stomach, and eyes when compared to young males. Respiration at CIV showed that old males have markedly elevated mitochondrial activity in the skeletal muscle (quadriceps, diaphragm, soleus, plantaris) and cecum, and reduced mitochondrial activity in the brain (cortex, cerebellum, hippocampus), BAT, liver, spleen, stomach, and iWAT, relative to young males (Figure 4C, right panel). A relative and global view of the age-specific differences across male mice showed that old males have significantly elevated mitochondrial activity in the skeletal muscles, mesWAT, GI tract, and heart, with a concomitant reduction in mitochondrial activity in the stomach, iWAT, gWAT, eyes, and nearly all brain regions (Figure 4D). Together, these data indicate age has a strong effect in modulating mitochondrial respiration in male mice.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_fig4.tif/full/max/0/default.jpg)
Tissue-by-tissue analysis of young and old male mitochondrial function.
A. (left) Systems-level view of mitochondrial respiration (NADH-stimulated) through complex I (CI). (right) Mitochondrial respiration through CI across all male tissues. B. (left) Systems-level view of mitochondrial respiration (Succinate-stimulated in the presence of rotenone to inhibit CI) through complex II (CII). (right) Mitochondrial respiration through CII across all male tissues. C. (left) Systems-level view of mitochondrial respiration at complex IV (CIV) in the presence of rotenone and antimycin A to inhibit CI and CIII, respectively. (right) Mitochondrial respiration at CIV across all male tissues. All data is presented as the mean with standard error and organized highest to lowest for old male values. D. Heat map view of mitochondrial function across all male tissues assayed. Data is presented as old/young male. Tissues with elevated respiration in old males appear red while the same for young males appear blue. Data is organized highest to lowest by summation of old male CI, CII, and CIV respiration values. n = 10 old male (OM, 80 weeks) and 10 young male (YM, 10 weeks) per tissue assayed. Statistical significance is represented as, a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001. BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; Vent, ventricles.
Effects of age on female mitochondrial function
The third tissue-by-tissue comparison of mitochondrial function was made between old and young female mice. Systems-level analysis of respiration via CI, CII, or CIV across all 33 tissues showed no significant differences in OCR distribution between old and young female mice (Figure 5A-C, left panel). Individual tissue comparisons, however, showed many significant differences in response to age. Respiration through CI showed that old females have elevated mitochondrial activity in the heart ventricles, skeletal muscles (quadriceps, diaphragm, soleus, tongue, and plantaris), stomach, and mesWAT, and a concomitant reduction in mitochondrial activity in the cerebellum when compared to young females (Figure 5A, right panel). Respiration through CII also showed that old females have increased mitochondrial respiration in the heart ventricles, skeletal muscles (quadriceps, diaphragm, plantaris), and mesWAT relative to young females (Figure 5B, right panel). In contrast, old females had reduced mitochondrial respiration via CII in the liver, brain (cortex and cerebellum), gWAT, fallopian tubes, duodenum, eyes, and pancreas when compared to young females. Respiration at CIV likewise showed that old females have elevated mitochondrial activity in the skeletal muscle (quadriceps, diaphragm, plantaris) and mesWAT relative to young females; concomitantly, old females had reduced mitochondrial activity in the brain (cortex and cerebellum), liver, gWAT, stomach, lung, eyes, duodenum, and skin when compared to young females (Figure 5C, right panel). A relative and global view of the age-specific differences across female mice showed that old females have elevated mitochondrial respiration in the skeletal muscles, mesenteric fat, and heart ventricle, and a concomitant reduction in mitochondrial activity in the eyes, skin, duodenum, gWAT, iWAT, and nearly all brain regions when compared to young females. Similar to males, these data also indicate age has a strong effect in modulating mitochondrial activity in female mice.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_fig5.tif/full/max/0/default.jpg)
Tissue-by-tissue analysis of young and old female mitochondrial function.
A. (left) Systems-level view of mitochondrial respiration (NADH-stimulated) through complex I (CI). (right) Mitochondrial respiration through CI across all female tissues. B. (left) Systems-level view of mitochondrial respiration (Succinate-stimulated in the presence of rotenone to inhibit CI) through complex II (CII). (right) Mitochondrial respiration through CII across all female tissues. C. (left) Systems-level view of mitochondrial respiration at complex IV (CIV) in the presence of rotenone and antimycin A to inhibit CI and CIII, respectively. (right) Mitochondrial respiration at CIV across all female tissues. All data is organized highest to lowest for old female values. D. Heat map view of mitochondrial function across all female tissues assayed. Data is presented as old/young female, so tissues with elevated mitochondrial respiration in old females appear red while the same for young females appear blue. Data is organized highest to lowest by summation of old female CI, CII, and CIV respiration values. n = 10 old female (OF, 80 weeks) and 10 young female (YF, 10 weeks) per tissue assayed. Statistical significance is represented as, a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001. BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; Vent, ventricles.
Age differentially affects mitochondrial function in male and female mice
The fourth tissue-by-tissue comparison of mitochondrial function was made between old male and female mice, where we focused on the effects of sex on mitochondrial respiration in old mice. A systems-level view of respiration through CI, CII, or CIV across all 33 tissues showed no differences in OCR distribution across sex in old mice (Figure 6A-C, left panel). At the individual tissue level, however, old male mice had greater mitochondrial activity via CI in the heart atria, kidney medulla, and soleus muscle as compared to old females. Respiration through CII showed that old males have higher mitochondrial activity in the kidney (cortex and medulla) and pancreas, and reduced mitochondrial activity in the stomach, relative to old females (Figure 6B, right panel). Respiration at CIV showed that old males have higher mitochondrial respiration in the kidney medulla, soleus muscle, and lungs, and reduced mitochondrial activity in the cerebellum and mesWAT, when compared to old females (Figure 6C, right panel). A global and relative view of the sex-specific differences across age showed that old males have elevated mitochondrial activity in the distal colon, lung, eyes, pancreas, kidney, and heart when compared to old females, whereas old females have higher mitochondrial activity in all adipose tissue depots, stomach, and nearly all brain regions when compared to old males (Figure 6D).
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_fig6.tif/full/max/0/default.jpg)
Tissue-by-tissue analysis of old male and female mitochondrial function.
A. (left) Systems-level view of mitochondrial respiration (NADH-stimulated) through complex I (CI). (right) Mitochondrial respiration through CI across all old tissues. B. (left) Systems-level view of mitochondrial respiration (Succinate-stimulated in the presence of rotenone to inhibit CI) through complex II (CII). (right) Mitochondrial respiration through CII across all tissues. C. (left) Systems level view of mitochondrial respiration at complex IV (CIV) in the presence of rotenone and antimycin A to inhibit CI and CIII, respectively. (right) Mitochondrial respiration at CIV across all tissues. All data is presented as the mean with standard error and organized highest to lowest for male values. D. Heat map view of mitochondrial function across all tissues assayed. Data is represented as old male/female, so tissues with elevated mitochondrial respiration in males appear red while the same for females appear blue. Data is organized highest to lowest by summation of male CI, CII, and CIV respiration values. n = 10 old male (OM, 80 weeks) and 10 old female (OF, 80 weeks) per tissue assayed. Statistical significance is represented as, a = p < 0.05, b = p < 0.01, c = p < 0.001, and d = p < 0.0001. BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; Vent, ventricles
Age has a much larger effect than sex on mitochondrial function
To assess the relative contributions of sex and age to mitochondrial respiration, we first counted the total number of significant differences from all cross-group comparisons made in Figures 3-6, which was 98 in total. Clustering significant differences by the type of respiration affected showed CIV to have the most with 39 differences, followed by CII with 38 differences, and CI with 21 differences (Figure 7A).
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Mitochondrial respiration is affected by sex but dominated by age.
A. Total number of statistically significant differences across all tissue-by-tissue comparisons, grouped by the component measured (CI = respiration through complex I, CII = respiration through complex II, or CIV = respiration through complex IV). B. Total number of significant differences across tissue-by-tissue comparisons grouped by the specific comparison, colored to represent the mitochondrial component affected (CI, CII, or CIV), and summed to the right of each histogram to highlight the number of significant findings per comparison. To underscore the number of statistically significant sex- or age-associated differences, the total number of significant findings from YM-by-YF and OM-by-OF (sex effect), and OM-by-YM and OF-by-YF (age effect) were summed. C. Quantification of the total number of tissues affected in each tissue-by-tissue comparison. Data are colored based on the specific comparison and grouped as sex- or age-associated to illustrate the effect-type. D. Cumulative absolute difference of means for CI, CII, and CIV (from left to right) grouped by effect-type, sex (originating from YM-by-YF or OM-by-OF) or age (originating from OM-by-YM or OF-by-YF). These graphs do not indicate directionality of the change, only the absolute cumulative magnitude. Each box within the histogram represents a unique tissue. All histograms are organized lowest (left) to highest (right) in degree of tissue contribution to total change given the comparison type. The top contributors to sex- or age-associated changes are highlighted with non-greyscale colors and their relative percentage of contribution to the total cumulative difference is provided. E. Principal Component Analysis (PCA) of all tissues and groups for CI, CII, and CIV (from left to right). F. Pearson correlation heat maps of all tissues combined from young and old, male and female mice. From top to bottom and left to right the samples are organized by group as follows: YF, YM, OF, and OM (n = 10 mice per group). YM = young male, YF = young female, OM = old male, OF = old female. Young = 10 weeks, Old = 80 weeks. BAT, brown adipose tissue; gWAT, gonadal white adipose tissue; iWAT, inguinal white adipose tissue; Quad, quadriceps muscles; At, atria; Vent, ventricles; Diaphr, diaphragm muscle; Med, kidney medulla.
Grouping significant differences by the cross-group comparison in which they occurred showed that young male (YM)-by-old male (OM) have the most significant differences with 37 in total, followed by young female (YF)-by-old female (OF) with 35, YM-by-YF with 14, and OM-by-OF with 12 significant differences (Figure 7B). Clustering the significant difference counts by type, sex (originating from YM-by-YF or OM-by-OF) or age (originating from YM-by-OM or YF-by-OF), we saw that although both sex and age exerted an effect on mitochondrial respiration, it was age that resulted in the highest number of significant changes (Figure 7B). We next sought to quantify the number of tissues significantly affected in at least one mitochondrial parameter per cross-group comparison. There were eight tissues with a difference when comparing young male and female, 10 when comparing old male and female, and 21 tissues when comparing young and old male, or young and old female (Figure 7C). Together, these data indicate that the majority of significant differences observed are the result of age.
Next, we calculated the absolute difference of means and summed the resultant values based on their effect-type, sex (originating from YM-by-YF or OM-by-OF) or age (originating from YM-by-YF or OM-by-OF) (Figure 7D). This analysis offered an added magnitude perspective to our view of changes in mitochondrial respiration across sex and age. It allowed us to see that respiration via CI, CII, and CIV all have a greater magnitude of difference as a result of age as compared to sex. Each graph in Figure 7D shows ranked values (lowest/left to highest/right) within the age and sex groupings with the top tissues colored and labeled with their percent contribution to the total. The highest contributors to the differences in respiration via CI as a result of age were heart (ventricles and atria), BAT, and quadriceps muscles, while those for sex are heart (ventricles and atria) and BAT. The highest contributors to the differences in respiration through CII as a result of age were heart ventricles, BAT, quadriceps, and diaphragm, while those for sex are heart (ventricles and atria), kidney (cortex and medulla), and BAT. The highest contributors to the differences in respiration at CIV as a result of age were heart (ventricles and atria), BAT, quadriceps, and diaphragm, while those for sex were BAT and heart (ventricles and atria). It is important to note that these rankings do not indicate directionality of a difference, only total magnitude. Additionally, these changes are represented as absolute magnitude of difference. Therefore, tissues with lower absolute oxygen consumption values would skew towards lower ranking, even though the relative change occurring within that tissue may be large.
Principle component (PC) analysis of each mitochondrial respiration dataset showed a primary and consistent separation across PC1 as a result of age (Figure 7E). A small percentage of the variance can be explained through PC2 as a result of sex, although this effect was not as consistent as that seen with age. Pearson correlation heat maps further highlighted age as a key factor relating samples across groups (Figure 7F). Male and female samples of the same age positively correlated with one another, while young and old samples regardless of sex showed a negative correlation. These combined data indicate that while sex does affect mitochondrial respiration, age is the dominant factor.
The sex-specific impact of age on mitochondrial function
To investigate the sex-dependent effects on mitochondrial function across age, we first calculated all of the relative change values for males and females from young to old. Summation of relative change values of all tissues within a specific mitochondrial parameter—respiration through CI, CII, or CIV—allowed us to view sex-specific systems-level effects across age (Figure 8A-B). Both the male and female systems showed a relative net increase in CI and decrease in CIV activity with age. Interestingly, with respect to CII activity, the male and female systems had divergent response. The net relative CII activity increased in males and decreased in females with age. These data suggest that: 1) independent of sex, CI and CIV are uniquely regulated, showing net opposite responses with age, and 2) CII activity is the most sex-affected respiratory component across age and tissues.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_fig8.tif/full/max/0/default.jpg)
The effects of age on mitochondrial respiration occur in sex-specific ways.
A-B. Systems-level view of the total relative change (sum of all relative changes) present at each mitochondrial parameter (respiration via CI, CII, or CIV) for males (M) and females (F), respectively. All change is old (O) compared to young (Y). C. Heat maps of O / Y data for each mitochondrial parameter per tissue across lifespan. Male and female values are grouped and organized by greatest (top) to least (bottom) sum of relative change per tissue. Tissues with the largest positive relative change as a result of aging are located on the top-most region of the heat maps, while those with the largest negative relative change are at the bottom. The middle of each heat map represents tissues with little relative response to aging or with opposite effect directions across sex. D. Graphs showing magnitude of sex-effect with age across all tissues and mitochondrial parameters (CI, CII, or CIV). The blue line and circles represent log2(old male/young male) data and the red line and boxes represent log2(old female/young female) data; both linked to the left y-axis. The black line and triangles represent the absolute difference of male and female relative change data (linked to the right y-axis). All data is organized from left to right by highest to lowest absolute difference of relative change across sex. Tissues with the greatest relative difference across sex are located to the left-most region of the graph, while those with the most similar response to aging are located to the right. A hollow blue circle, red box, and black triangle represent a tissue with a divergent sex-specific aging response. E. Summary diagrams classifying the relative trends of each mitochondrial parameter assayed per tissue as age- or age-and-sex-specific. Age-specific effects have a shared relative change direction across sex. Tissues in the red “Shared Increase” box have a positive relative change for both males and females. Tissues in the blue “Shared Decrease” box have a negative relative change for both males and females. Tissues in the Purple box labeled “Divergent” have opposing log2(O/Y) directions (signs, + or -) for male and female values; these tissues display relative mitochondrial changes that are age-and-sex-specific. F. Summary diagram showing tissues with a shared increase (red box) or decrease (blue box) consistent across all complexes (CI, CII, and CIV). Tissues within the shared increase or decrease classifications are grouped by their tissue-type, for example. PL, DI, QD, SL, and HV are all muscle, CO, HI, HY, and CE are all brain and so on. CI = respiration measured through complex I stimulated by NADH; CII = respiration through complex II stimulated by succinate in the presence of rotenone; CIV = respiration at complex IV stimulated by TMPD and ascorbate in the presence of rotenone and antimycin A. Tissues: BT = brown adipose tissue, CC = cecum, CE = cerebellum, CO =brain cortex, DI = diaphragm, DC = distal colon, DU = duodenum, EY = eyes, GS = gastrocnemius, GW = gonadal white adipose tissue, HS = hamstring, HA = heart atria, HV = heart ventricles, HI = hippocampus, HY = hypothalamus, IL = ileum, IW = inguinal white adipose tissue, JE = jejunum, KC = kidney cortex, KM = kidney medulla, LV = liver, LN = lung, MW = mesenteric white adipose tissue, PN = pancreas, PL = plantaris, PC = proximal colon, QD = quadriceps, SK = skin, SL = soleus, SP = spleen, ST = stomach, TN = tongue. Reproductive organs are omitted from cross-sex analysis.
Heat maps of the individual tissue-level data presented in Figure 8A-B further highlight the tissue-level similarities and differences across age, sex, and mitochondrial respiration type (i.e., through CI, CII, or CIV). For example, respiration through CI, CII, or CIV showed that the plantaris muscles (PL), diaphragm muscle (DI), quadriceps muscles (QD), jejunum (JE), and mesenteric white adipose tissue (MW) have the greatest positive relative change in response to age, while the eye (EY), gonadal white adipose tissue (GW), skin (SK), and stomach (ST) were among the tissues that showed the greatest negative relative change with age (Figure 8C).
To determine the tissues with the strongest sex-specific age effects, we organized male and female data by the largest (left) to smallest (right) difference of relative change. This multi-dimensional view highlights differences within a tissue across sex in response to age (Figure 8D). The largest sex-specific effects of age on respiration via CI were found in the stomach (ST), jenujum (JE), distal colon (DC), quadriceps muscles (QD), and pancreas (PN); in contrast, the kidney cortex (KC), cecum (CC), cerebellum (CE), soleus muscle (SL), and diaphragm muscle (DI) displayed the most similarity of change (Figure 8D, top panel). The largest sex-specific effects of age on respiration through CII were found in the stomach (ST), duodenum (DU), distal colon (DC), pancreas (PN), and jejunum (JE); in contrast, the liver (LV), skin (SK), hamstring muscle (HS), kidney medulla (KM), and tongue (TN) displayed the smallest sex-differences (Figure 8D, middle panel). Finally, the most sex-specific effects of age on respiration through CIV were found in mesenteric white adipose tissue (MW), jejunum (JE), duodenum (DU), distal colon (DC), and skin (SK); in contrast, the tongue (TN), heart ventricles (HV), gastrocnemius muscle (GS), distal colon (DI), and brain cortex (CO) displayed the greatest similarity of change with age (Figure 8D, bottom panel).
All sexually divergent tissues are marked specifically within each graph per mitochondrial respiration-type. Respiration via CI showed 5 tissues with sexual divergence in response to aging, and these were stomach (ST), distal colon (DC), pancreas (PN), lung (LN), and kidney medulla (KM) (Figure 8D, top panel). Respiration through CII showed 5 tissues with sexual divergence in response to aging, and these were duodenum (DU), pancreas (PN), lung (LN), heart atria (HA), and tongue (TN) (Figure 8D, second panel). Respiration at CIV also showed 5 tissues with sexual divergence in response to aging, and these were jejunum (JE), distal colon (DC), hamstring (HS), heart atria (HA), and kidney medulla (KM) (Figure 8D, bottom). Together, these data show the relative magnitude of change across sex and age, and highlight the tissue- and sex-specific regulation of mitochondrial respiration with aging.
We further grouped the above data by directionality to visualize male and female tissue responses to aging (Figure 8E). From this, we can quickly visualize tissues displaying a shared direction of change in respiration via CI, CII, or CIV across sex and age. Additionally, some tissues responded in an age-and-sex-specific manner (i.e., display divergence in Figure 8D). This data clustering summarizes the shared (age-specific) or opposite (sex-specific) directionality of mitochondrial function across tissues in respond to age.
It should be noted, however, that the mitochondrial activity of a particular tissue could increase or decrease in a sex-specific way even though the directionality is the same. For example, respiration through CII for the stomach (ST) showed male and female values decreasing with age, yet the male had a larger relative decrease when compared to female (Figure 8D, middle panel). Another consideration should be given to the divergent group with varying degrees of divergence. For example, CI-associated respiration of the stomach (Figure 8D, top panel) showed a strong divergence given that male had a strong decline in function while the female increased over time. On the other hand, the CI-associated respiration of the kidney medulla showed a weak divergence; although the directionality of change was opposite, the magnitude was small.
Lastly, we grouped all the tissues with a consistent shared (across sex) relative increase or decrease in CI-, CII-, and CIV-associated respiration in response to age (Figure 8F). The tissues with a shared (across sex) increased response to aging were plantaris (PL), quadriceps (QD), diaphragm (DI), soleus (SL), heart ventricle (HV), ileum (IL), cecum (CC), proximal colon (PC), and mesenteric fat (MW). Interestingly, PL, QD, DI, and SL are all skeletal muscles and IL, CC, and PC are all part of the digestive tract. Also of note, the gastrocnemius (GT), hamstring (HS), and tongue (TN) muscles were not uniformly increasing with age. In fact, these muscles showed reduced mitochondrial respiration with age, in striking contrast to other skeletal muscle types assayed. The tissues with a shared (across sex) decrease in response to aging were brown fat (BT), gonadal fat (GW), inguinal fat (IW), brain cortex (CO), hippocampus (HI), hypothalamus (HY), cerebellum (CE), liver (LV), kidney cortex (KC), eye (EY), skin (SK), and spleen (SP). Different fat depots and many of the brain regions showed a consistent decline in respiratory function with age, regardless of sex. The kidney cortex (KC) oddly showed a respiratory effect distinct from the medulla, which was almost completely resistant to age-related respiratory changes. The eyes (EY) not only showed a consistent decline in respiration with age, but also had one of the largest combined relative effects. Together, the shared and divergent analyses presented (Figure 8E and F) illuminate the modulation of mitochondrial function across age.
Discussion
Here, we provide the most comprehensive catalog of sex- and age-associated mitochondrial respiration signatures across diverse tissues and organs system. One important aspect of our study to emphasize is the experimental uniformity. All the tissue samples were collected from the same set of mice, and processed and analyzed in a uniform and standardized manner on the same respirometry platform in a single laboratory. Combined with the ten biological replicates, our experimental setup and workflow markedly enhanced the rigor and reduced the variations in data quality. From the mitochondrial respiration compendium, we can clearly see that mitochondrial function varies widely across tissues and that aging has a much larger effect than sex on mitochondrial activity across tissues.
The transcriptomic dataset generated by the Tabula Muris Consortium clearly indicates organ-specific temporal signatures across the lifespan (7–9), and this is assumed to track closely with tissue function even though no equivalent systematic interrogation of tissue function across the lifespan has been performed. In this regard, our mitochondrial activity atlas aligned and corroborated with the conclusion from large-scale transcriptomic analyses that the aging process and trajectory can vary substantially across tissues (7, 8). This reinforces the notion that while an organism ages, the aging-associated decline in organ function is not uniform across tissues and organ systems. Given that genetics and environmental factors all contribute to tissue health and their functional breakdown with age, this further amplifies the heterogenous process of aging across a population.
Although sex is a significant biological variable influencing many aspects of physiology and pathophysiology (29, 30), we were surprised that sex has a relatively modest impact on respiratory capacity in mitochondria across tissues and age. The modest impact of sex on mitochondrial respiration across tissues is also consistent with the relatively minor impact of sex on tissue transcriptome across the lifespan (7, 11). The caveat, however, is that our study is based on a single strain of mice with a uniform genetic background. The contribution of biological sex may be more pronounced in an outbred population where sex hormones interact with other genetic and environmental determinants to influence mitochondrial activity across tissues and age.
Aging is a dynamic process that unfolds across the lifespan, and this involves changes at the molecular, cellular, biochemical, and tissue level. Transcriptomics analyses have consistently shown that aging induces a reduction in mitochondrial OXPHOS genes (7, 8), and this likely contributes to the reduced mitochondrial activity we observed across many tissues in old mice. Changes in cell function, however, are often counter measured by homeostatic responses. While many tissues showed a significant reduction in mitochondrial function, some tissues also showed a concomitant increase in mitochondrial activity with age. With the assumption that organ function declines with age, our data suggests a potential organ-selective compensatory response to declining efficiency in cellular function which entails a greater demand on mitochondrial ATP production. This hypothesis awaits future experimental confirmation.
Every respirometry method has its advantages and limitations (27). Unlike the mitochondrial respiration analysis in intact cells or isolated mitochondria, our respirometry analysis was performed in mitochondria-enriched lysate derived from frozen tissues (28). In an intact mitochondrion, the rate of mitochondrial respiration is regulated by both substrate supply across the mitochondrial membrane and the rate of NADH and FADH production via the TCA cycle and fatty acid β-oxidation. In the absence of an intact mitochondrial membrane, our assays measure maximal mitochondrial respiration through CI, CII, or CIV. Thus, our mitochondrial activity reflects maximal respiration across tissues. In an in vivo milieu, mitochondrial activity is likely regulated and may not reach its maximal capacity as reflected in our assay. However, the advantage of the frozen-tissue method makes it feasible to carry out large-scale respirometry analyses, which outweigh its limitations.
In summary, our mitochondrial functional signatures demonstrate similar and divergent responses to aging across tissues. Whether changes in tissue mitochondrial respiration reflect the cause, consequence, or both, of aging remains to be determined. We anticipate that the integration of this knowledge with other large-scale omics data will help uncover potential genetic, epigenetic, and biochemical mechanisms linking mitochondrial health and organismal aging.
Materials and methods
Mouse model
All wild-type C57BL/6J male and female mice were purchased from the Jackson Laboratory and fed a standard chow (Envigo; 2018SX). In total, the young group was comprised of 10 male and 10 female 8-week-old mice, and the old group was comprised of 10 male and 10 female 80-week-old mice. Mice were housed in polycarbonate cages on a 12h:12h light-dark photocycle with ad libitum access to water and food. All mice were fasted for 2 h prior to euthanasia and dissection. Tissues were collected, snap-frozen in liquid nitrogen, and kept at −80°C until analysis. All mouse protocols were approved by the Institutional Animal Care and Use Committee of the Johns Hopkins University School of Medicine (animal protocol # MO22M367). All animal experiments were conducted in accordance with the National Institute of Health guidelines and followed the standards established by the Animal Welfare Acts.
Comprehensive multi-organ dissection
Each mouse was dissected cleanly, swiftly, and in a concerted manner by three people. Each mouse dissection took approximately 8-10 min, with 33 tissues collected per dissection. After euthanasia, blood was collected via decapitation. The head was then immediately given to dissector one to collect brain regions (hypothalamus, cerebellum, hippocampus, and cortex), eyes, and tongue. Simultaneously, the visceral cavity was opened by dissector two. Inguinal white adipose tissue (iWAT) was collected immediately after opening the abdominal skin. After that the abdominal muscle was cut and gonadal white adipose tissue (gWAT) and testes or fallopian tubes were collected. Following this, the visceral organs were partitioned in two groups. Dissector two promptly dissected liver, stomach, kidneys (further separated the cortex and medulla), spleen, diaphragm, heart (further divided into atria and ventricles), lungs, brown adipose tissue (BAT), and skin (cleared of hair using Topical Nair lotion, cleaned, then collected). At the same time, dissector three was collecting the pancreas, mesenteric white adipose tissue (mesWAT), small intestine (further split into duodenum, jejunum, and ileum), cecum, and large intestine (further split into proximal and distal colon). As soon as tissue collection in the head was finished, the mouse carcass was cut transversely at the lumbar spine and handed to dissector one for muscle dissection. Dissector one then rapidly and precisely anatomized (bilaterally) the quadriceps (entire complex – rectus femoris, vastus lateralis, vastus intermedius, and vastus medialis), hamstrings (biceps femoris), gastrocnemius, plantaris, and soleus muscles. All tissues were washed with sterile 1X PBS to remove residual blood prior to snap freeze. Additionally, the stomach, small intestine, and large intestine were cleared and cleaned of debris with PBS prior to freezing. The Cecum, however, was kept whole containing all fecal/food matter and microorganisms present. All dissected tissues were snap frozen in liquid nitrogen, and stored at −80°C for later analysis.
Respirometry of frozen tissue samples
Respirometry was conducted on frozen tissue samples to assay for mitochondrial activity as described previously (28), using a Seahorse XFe96 Analyzer. Samples were thawed in 1X MAS buffer (70 mM sucrose, 220 mM mannitol, 5 mM KH2PO4, 5 mM MgCl2, 1 mM EGTA, 2 mM HEPES pH 7.4), finely minced with scissors, then homogenized with a glass Dounce homogenizer on ice. The entire sample, bilateral for skeletal muscles, was homogenized and used for respirometry with the exception of liver in which only a piece was homogenized. This was done to provide a true tissue average and avoid regional differences in mitochondria. The resulting homogenate was spun at 1000 g for 10 min at 4°C. The supernatant was collected and immediately used for protein quantification by BCA assay (Thermo Scientific, 23225). Each well of the Seahorse microplate was loaded with the designated amount (in µg) of homogenate protein (Table 1). Each biological replicate is comprised of three technical replicates. Samples from all tissues were treated separately with NADH (1 mM) as a complex I substrate or Succinate (a complex II substrate, 5 mM) in the presence of rotenone (a complex I inhibitor, 2 µM), then with the inhibitors rotenone (2 µM) and Antimycin A (4 µM), followed by TMPD (N,N,N’,N’-Tetramethyl-p-Phenylenediamine; also known as Wurster’s Reagent, 0.45 mM) and Ascorbate (Vitamin C, 1 mM) to activate complex IV, and finally treated with Azide (40 mM) to assess non-mitochondrial respiration.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_tbl1.tif/full/max/0/default.jpg)
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_tbl1a.tif/full/max/0/default.jpg)
Assay parameters for Seahorse-based respirometry analysis across all tissues.
Table shows tissues used, approximate size per tissue homogenized for analysis, amount of 1X MAS buffer used for homogenization, and the amount of protein used for respiration analysis across all tissues.
Quantification of mitochondrial content
Mitochondrial content of homogenates used for respirometry was quantified with MitoTracker Deep Red FM (MTDR, Invitrogen, M22426) staining as described previously (28). Briefly, lysates were incubated with MTDR (1 µM) for 10 min at 37°C, then centrifuged at 2000 g for 5 min at 4°C. The supernatant was carefully removed and replaced with 1X MAS solution and fluorescence was read with excitation and emission wavelengths of 625 nm and 670 nm, respectively. All measurements were read with a BioTek Synergy HTX Multimode Plate Reader (Agilent). All samples from a single tissue-type were measured on the same plate, in duplicate, with an equal gain setting of 90 to ensure comparability across samples. To minimize non-specific background signal contribution, control wells were loaded with MTDR + 1X MAS and subtracted from all sample values.
Acknowledgements
This work was supported by the National Institutes of Health (DK084171 to GWW). D.C.S. was supported by an NIH T32 training grant (HL007534).
Competing interests
We declare that none of the authors has a conflict of interest.
Data availability
All the data presented are included in the main text or as supplementary tables and figures.
Abbreviations
BAT: Brown adipose tissue
CI: Mitochondrial complex I
CII: Mitochondrial complex II
CIII: Mitochondrial complex IIII
CIV: Mitochondrial complex IV
FADH: flavin adenine dinucleotide
gWAT: Gonadal white adipose tissue
iWAT: Inguinal white adipose tissue NADH nicotinamide adenine dinucleotide OCR Oxygen consumption rate
Rot: Rotenone
TMPD: N,N,N’,N’-Tetramethyl-p-Phenylenediamine
Supplemental figure legends
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s1.tif/full/max/0/default.jpg)
Mitochondrial respiration of brown adipose tissue (BAT) across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s2.tif/full/max/0/default.jpg)
Mitochondrial respiration of cecum across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s3.tif/full/max/0/default.jpg)
Mitochondrial respiration of brain cerebellum across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s4.tif/full/max/0/default.jpg)
Mitochondrial respiration of brain cortex across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s5.tif/full/max/0/default.jpg)
Mitochondrial respiration of diaphragm muscle across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s6.tif/full/max/0/default.jpg)
Mitochondrial respiration of distal colon across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s7.tif/full/max/0/default.jpg)
Mitochondrial respiration of duodenum across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s8.tif/full/max/0/default.jpg)
Mitochondrial respiration of eyes across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s9.tif/full/max/0/default.jpg)
Mitochondrial respiration of fallopian tubes and testicles across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the two primary comparisons are 1) young (10 weeks) female vs. old (80 weeks) female, 2) young male (10 weeks) vs. old (80 weeks) male. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s10.tif/full/max/0/default.jpg)
Mitochondrial respiration of gastrocnemius muscle across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s11.tif/full/max/0/default.jpg)
Mitochondrial respiration of gonadal white adipose tissue (gWAT) across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s12.tif/full/max/0/default.jpg)
Mitochondrial respiration of hamstring (biceps femoris) muscles across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s13.tif/full/max/0/default.jpg)
Mitochondrial respiration of heart atria across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s14.tif/full/max/0/default.jpg)
Mitochondrial respiration of heart ventricles across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s15.tif/full/max/0/default.jpg)
Mitochondrial respiration of brain hippocampus across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s16.tif/full/max/0/default.jpg)
Mitochondrial respiration of brain hypothalamus across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s17.tif/full/max/0/default.jpg)
Mitochondrial respiration of ileum across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, *** p < 0.001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s18.tif/full/max/0/default.jpg)
Mitochondrial respiration of inguinal white adipose tissue (iWAT) across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s19.tif/full/max/0/default.jpg)
Mitochondrial respiration of jejunum across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. ** p < 0.01. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s20.tif/full/max/0/default.jpg)
Mitochondrial respiration of kidney cortex across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. ** p < 0.01. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s21.tif/full/max/0/default.jpg)
Mitochondrial respiration of kidney medulla across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s22.tif/full/max/0/default.jpg)
Mitochondrial respiration of liver across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s23.tif/full/max/0/default.jpg)
Mitochondrial respiration of lung across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s24.tif/full/max/0/default.jpg)
Mitochondrial respiration of mesenteric white adipose tissue (MesWAT) across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s25.tif/full/max/0/default.jpg)
Mitochondrial respiration of pancreas across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s26.tif/full/max/0/default.jpg)
Mitochondrial respiration of plantaris muscles across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s27.tif/full/max/0/default.jpg)
Mitochondrial respiration of proximal colon across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s28.tif/full/max/0/default.jpg)
Mitochondrial respiration of Quadricep muscle complex across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s29.tif/full/max/0/default.jpg)
Mitochondrial respiration of skin across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s30.tif/full/max/0/default.jpg)
Mitochondrial respiration of soleus muscles across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s31.tif/full/max/0/default.jpg)
Mitochondrial respiration of spleen across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s32.tif/full/max/0/default.jpg)
Mitochondrial respiration of stomach across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs1s33.tif/full/max/0/default.jpg)
Mitochondrial respiration of tongue across sex and age.
A. Average oxygen consumption rate (OCR) traces per group, normalized to the amount of tissue homogenate protein input. From left to right the four primary comparisons are 1) young (10 weeks) male vs. young female, 2) old (80 weeks) male vs. old female, 3) young male vs. old male, and 4) young female vs. old female. Each group tracing represents the average trace of n = 10 samples. Each tracing shows the entire process of the Seahorse-based respirometry assay with injection compounds listed at the time of introduction to the sample. The sequence is as follows: i) basal reads, ii) addition of NADH (activation of respiration through complex I), iii) addition of antimycin A (AA, inhibitor of complex III) and rotenone (Rot, inhibitor of complex I), iv) addition of TMPD and ascorbate (to activate complex IV via electron donation to cytochrome c), and finally v) addition of azide (inhibitor of complex IV). B. The same information as presented in (A) conducted on the same samples, but the NADH injection step is replaced with the injection of succinate (to activate respiration through complex II) and rotenone (to inhibit complex I). C. Average values of all data presented in (A) and (B). Each dot represents the average of three technical replicates measured at three separate times. Both independent measurements of complex IV (CIV) were used to determine average CIV respiration. D. Average respiration values normalized to mitochondrial content as determined by MitoTracker Deep Red (MTDR) staining. E. Mitochondrial content quantification per group. n = 10 mice per group. * p < 0.05, ** p < 0.01, **** p < 0.0001. CI = complex I, CII = complex II, CIV = complex IV. YM = young male, YF = young female, OM = old male, OF = old female.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s1.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in the brain across sex and age.
A. Depiction of whole mouse brain denoting the specific regions assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all brain regions assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 40 samples. Data point color indicates the specific brain region, and bar color indicates the group. C. Individual brain region average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are four background colors indicating brain region (from left to right: cerebellum (CE), cortex (CO), hippocampus (HI), and hypothalamus (HY)). D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old- dominant effect (respectively) within a specific brain region. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s2.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in the kidneys across sex and age.
A. Depiction of the kidney regions assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all kidney regions assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 20 samples. Data point color indicates the specific kidney region, and bar color indicates the group. C. Individual kidney region average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are two background colors indicating the specific region (from left to right: cortex then medulla). D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old-dominant effect (respectively) of a kidney region. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values. KC = kidney cortex, KM = kidney medulla; both regions collected and assayed bilaterally.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s3.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in the heart across sex and age.
A. Depiction of the heart regions assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all heart regions assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 20 samples. Data point color indicates the specific heart region, and bar color indicates the group. C. Individual heart region average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are two background colors indicating the specific region (from left to right: atria then ventricles). D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old-dominant effect (respectively) of a heart region. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values. HA = heart atria (both left and right), HV = heart ventricles (both left and right).
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s4.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in skeletal muscle across sex and age.
A. Depiction of the skeletal muscles assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all skeletal muscles assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 70 samples. Data point color indicates the specific skeletal muscle, and bar color indicates the group. C. Individual skeletal muscle average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are seven background colors indicating the specific skeletal muscle [from left to right: diaphragm (DI), soleus (SL), tongue (TN), plantaris (PL), quadriceps (QD), hamstring (HS), and gastrocnemius (GS)]. D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old-dominant effect (respectively) of a skeletal muscle. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values. All muscles collected and assayed bilaterally.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s5.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in the white adipose tissue across sex and age.
A. Depiction of white adipose tissue (WAT) regions assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all WAT regions assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 30 samples. Data point color indicates the specific WAT region, and bar color indicates the group. C. Individual WAT region average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are three background colors indicating the specific region (from left to right: gonadal WAT, inguinal WAT, mesenteric WAT). D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old-dominant effect (respectively) of a WAT region. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values. gW = gonadal WAT, iW = inguinal WAT, mW = mesenteric WAT.
![](https://prod--epp.elifesciences.org/iiif/2/96926%2Fv1%2Fcontent%2F586781v1_figs2s6.tif/full/max/0/default.jpg)
Tissue-centric view of mitochondrial changes in the gastrointestinal tract across sex and age.
A. Depiction of the gastrointestinal tract (GI) denoting the specific regions assayed in this study. B. Average mitochondrial respiration through complex I (CI), respiration through complex II (CII), and respiration at complex IV (CIV) for all GI regions assayed. Data are grouped by sex and age (young (10 weeks) male, young female, old (80 weeks) male, old female which are represented as YM, YF, OM, and OF, respectively). Each data point represents the average of n = 10 mice, each bar represents n = 70 samples. Data point color indicates the specific GI region, and bar color indicates the group. C. Individual GI region average values of each group. Each bar represents the average of n = 10 mice. Under each mitochondrial parameter assayed (CI, CII, and CIV), there are seven background colors indicating the specific GI region (from left to right: stomach, duodenum, jejunum, ileum, cecum, proximal colon, and distal colon). D. Graphs depicting the total change in CI, CII, and CIV (from left to right) as a result of sex or age. Light blue or light grey bars to the left of the butterfly plot indicate a male- or young-dominant effect (respectively), while the light red and dark grey bars to the right indicate a female- or old-dominant effect (respectively) within a specific GI region. Male values were calculated by averaging young and old male. Female values were calculated by averaging young and old female. Young values were calculated by averaging young male and female. Old values were calculated by averaging old male and female. The change in a particular mitochondrial parameter was calculated by subtracting either the male and female or young and old values. ST = stomach, DU = duodenum, IL = ileum, JE = jejunum, CE = cecum, PC = proximal colon, DC = distal colon.
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