Chemoreception: Keeping carbon dioxide in check

The response of the brainstem to increased levels of carbon dioxide in the blood is coordinated with the response of the cardiovascular system.
  1. Alfredo J Garcia III
  2. Jan-Marino Ramirez  Is a corresponding author
  1. University of Chicago, United States
  2. Seattle Children's Research Institute, United States
  3. University of Washington School of Medicine, United States

Changes in the level of carbon dioxide molecules and hydrogen ions in the blood can change its pH, and this can have a negative impact on brain function. To avoid this, mammals rely on specialized cells in the brainstem called central chemoreceptors that can detect changes in the pH of the blood. When these chemoreceptors detect such a change, the body responds by regulating blood flow and breathing. However, changes in the rate at which blood flows through the brain make it more difficult to detect changes in its pH.

The pH of a liquid is determined by the concentration of hydrogen ions in it: the higher the concentration of hydrogen ions, the lower the pH. Carbon dioxide influences the pH of blood by reacting with water to form carbonic acid (H2CO3), which can dissociate to form a hydrogen ion (H+) and a hydrogen carbonate ion (HCO3-). Increasing the concentration of carbon dioxide in the blood therefore results in more H+ ions and a lower pH. However, both these reactions are reversible, and breathing heavily to remove carbon dioxide from the body will lead to a reduction in the concentration of the H+ and HCO3- ions, and hence to an increase in pH.

For over a century, it was thought that all the blood vessels in the brain reacted to increased levels of carbon dioxide in the blood by becoming wider to increase blood flow. Now, in eLife, Daniel Mulkey of the University of Connecticut, Thiago Moreira of the University of Sao Paulo and colleagues – including Virginia Hawkins as first author – report that elevated levels of carbon dioxide (a condition known as hypercapnia) cause the blood vessels in the brainstem to become narrower, while the blood vessels in the rest of the brain become wider (Hawkins et al., 2017).

Although the magnitude of the narrowing observed in the brainstem is modest (the diameter of the arteriole is reduced by less than 10%), the phenomenon reported by Hawkins et al. is reminiscent of the way that a shortage of oxygen (a condition known as hypoxia) causes the small pulmonary arteries in the lung to become narrower. This process optimizes lung function by redirecting of blood flow to areas of the lung where there is little blood flow, thereby increasing the surface area for gas exchange (Ward and McMurtry, 2009). Similarly, the narrowing of the blood vessels in the brainstem caused by increased levels of carbon dioxide might, according to Hawkins et al., help the body to measure the levels of carbon dioxide and H+ ions in the blood more accurately.

While neurons throughout the brainstem are known to be involved in the detection of carbon dioxide and H+ ions (Guyenet et al., 2010), the neurons in two regions of the brainstem – the ventrolateral medulla and the retrotrapezoid nucleus – have a particularly significant role (Kumar et al., 2015). However, the discovery in 2010 that astrocytes (cells in the brain and spinal cord that are not neurons) were also involved in central chemoreception showed that the regulation of breathing was more complex than expected (Gourine et al., 2010). The results of the elegant study by Hawkins et al. are further evidence in support of such complexity.

These are exciting times for the field. For over a half of a century, the drive to understand central chemosensitivity has understandably been focused on the cellular and molecular substrates of the phenomenon. However, growing evidence supports the notion that central chemosensitivity is a property that emerges from concerted interactions across the multiple cell types in the neurovascular unit, and that physiological interactions have an important role. While the phenomenon reported by Hawkins et al. appears to be small in magnitude, its potential impact on physiology cannot be dismissed.

Further research is now needed to address a number of questions: Does the constriction of the blood vessels seen by Hawkins et al. influence the pH of the surrounding tissue? Does the constriction have an impact on the cellular physiology of the neurons and astrocytes in the neurovascular unit? And how do the blood vessels in other regions of the brainstem respond to high levels of carbon dioxide? Answering these questions could, ultimately, lead to a systems-level understanding of the mechanisms underlying central chemosensitivity, and thus provide insights into the variability of this process in both health and disease.

References

Article and author information

Author details

  1. Alfredo J Garcia III

    Institute for Integrative Physiology and the Section of Emergency Medicine, University of Chicago, Chicago, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-5620-7519
  2. Jan-Marino Ramirez

    1. Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, United States
    2. Department of Neurological Surgery, University of Washington School of Medicine, Seattle, United States
    For correspondence
    jan.ramirez@seattlechildrens.org
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5626-3999

Publication history

  1. Version of Record published:

Copyright

© 2017, Garcia et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 3,642
    views
  • 135
    downloads
  • 9
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Alfredo J Garcia III
  2. Jan-Marino Ramirez
(2017)
Chemoreception: Keeping carbon dioxide in check
eLife 6:e27563.
https://doi.org/10.7554/eLife.27563

Further reading

    1. Neuroscience
    Katie Morris, Edita Bulovaite ... Mathew H Horrocks
    Research Article

    The concept that dimeric protein complexes in synapses can sequentially replace their subunits has been a cornerstone of Francis Crick’s 1984 hypothesis, explaining how long-term memories could be maintained in the face of short protein lifetimes. However, it is unknown whether the subunits of protein complexes that mediate memory are sequentially replaced in the brain and if this process is linked to protein lifetime. We address these issues by focusing on supercomplexes assembled by the abundant postsynaptic scaffolding protein PSD95, which plays a crucial role in memory. We used single-molecule detection, super-resolution microscopy and MINFLUX to probe the molecular composition of PSD95 supercomplexes in mice carrying genetically encoded HaloTags, eGFP, and mEoS2. We found a population of PSD95-containing supercomplexes comprised of two copies of PSD95, with a dominant 12.7 nm separation. Time-stamping of PSD95 subunits in vivo revealed that each PSD95 subunit was sequentially replaced over days and weeks. Comparison of brain regions showed subunit replacement was slowest in the cortex, where PSD95 protein lifetime is longest. Our findings reveal that protein supercomplexes within the postsynaptic density can be maintained by gradual replacement of individual subunits providing a mechanism for stable maintenance of their organization. Moreover, we extend Crick’s model by suggesting that synapses with slow subunit replacement of protein supercomplexes and long-protein lifetimes are specialized for long-term memory storage and that these synapses are highly enriched in superficial layers of the cortex where long-term memories are stored.

    1. Neuroscience
    Samyogita Hardikar, Bronte Mckeown ... Jonathan Smallwood
    Research Article

    Complex macro-scale patterns of brain activity that emerge during periods of wakeful rest provide insight into the organisation of neural function, how these differentiate individuals based on their traits, and the neural basis of different types of self-generated thoughts. Although brain activity during wakeful rest is valuable for understanding important features of human cognition, its unconstrained nature makes it difficult to disentangle neural features related to personality traits from those related to the thoughts occurring at rest. Our study builds on recent perspectives from work on ongoing conscious thought that highlight the interactions between three brain networks – ventral and dorsal attention networks, as well as the default mode network. We combined measures of personality with state-of-the-art indices of ongoing thoughts at rest and brain imaging analysis and explored whether this ‘tri-partite’ view can provide a framework within which to understand the contribution of states and traits to observed patterns of neural activity at rest. To capture macro-scale relationships between different brain systems, we calculated cortical gradients to describe brain organisation in a low-dimensional space. Our analysis established that for more introverted individuals, regions of the ventral attention network were functionally more aligned to regions of the somatomotor system and the default mode network. At the same time, a pattern of detailed self-generated thought was associated with a decoupling of regions of dorsal attention from regions in the default mode network. Our study, therefore, establishes that interactions between attention systems and the default mode network are important influences on ongoing thought at rest and highlights the value of integrating contemporary perspectives on conscious experience when understanding patterns of brain activity at rest.