Introduction

General fluid intelligence (gF) is a current problem-solving ability, which shows high inter-individual differences in humans(Cattell & Raymond, 1963). At the beginning of the last century, Spearman(Spearman, 1904) proposed that some general or g factor contributes to our gF. One key component of gF is visuo-spatial intelligence, usually tested by visual materials, shows high g-loading(Colom et al., 2006; Deary et al., 2010; Jung & Haier, 2007). The exact neural mechanisms of the interplay of visuo spatial intelligence with gF remain yet unclear, though.

The“neuro-efficiency” hypothesis is one explanation for individual differences in gF (Haier et al., 1988). This hypothesis puts forward that the human brain’s ability to suppress irrelevant information leads to more efficient cognitive processing. Correspondingly, using a well-known visual motion paradigm (center-surround antagonism)(Liu et al., 2016; Tadin et al., 2003), Melnick et al found a strong link between suppression index (SI) of motion perception and the scores of the block design test (BDT, a subtest of the Wechsler Adult Intelligence Scale (WAIS), which measures the visuo-spatial component (3D domain) of gF (Melnick et al., 2013). Motion surround suppression (SI), a specific function of human extrastriate cortical region, middle temporal complex (hMT+), aligns closely with this region’s activities (Gautama & Van Hulle, 2001). Furthermore, hMT+ is a sensory cortex involved in visual perception processing (3D domain) (Cumming & DeAngelis, 2001). These findings suggest that hMT+ potentially plays a significant role in 3D visuo-spatial gF by facilitating the efficient processing of 3D visual information and suppressing irrelevant information. However, more evidence is needed to uncover how the hMT+ functions as a core region for 3D visuo-spatial intelligence.

Frontal cortex is usually recognized as the cognitive core region (Duncan et al., 2000; Gray et al., 2003). Strong connectivity between the cognitive regions suggests a mechanism for large-scale information exchange and integration in the brain(Barbey, 2018; Cole et al., 2012). Therefore, the potential conjunctive coding may overlap with the inhibition and/or excitation mechanism of hMT+. Taken together, we hypothesized that 3D visuo-spatial intelligence (as measured by BDT) might be predicted by the inhibitory and/or excitation mechanisms in hMT+ and the integrative functions connecting hMT+ with frontal cortex (Figure 1a).

Figure 1.

To investigate our hypothesis, this work conducted multi-level examination including biochemical (Glutamatergic - GABAergic in hMT+), regional-systemic (brain connectivity with hMT+ - based), and behavioral (visual motion function in hMT+) levels to reveal if hMT+ contributes to the 3D visuo-spatial component of gF. We employ ultra-high field (7T) magnetic resonance spectroscopy (MRS) technology to reliably resolve GABA and Glu concentrations(Ende, 2015; Liu et al., 2022; Song et al., 2021). To verify the specificity of hMT+, we used early visual cortex (EVC, primarily in V1) - based GABA/Glu as control as it mediates the 2D rather than 3D visual domain(Cumming & DeAngelis, 2001).

Our findings first demonstrate that GABAergic inhibition mechanisms (but not excitatory Glu) in hMT+ region relate to 3D visuo-spatial ability. Further, analysis of functional brain connectivity at rest reveals that the network (between MT+ and frontal cortex) relating to MT+ GABA and perceptual suppression contribute the visuo-spatial intelligence. Our results provide direct evidence that inhibitory mechanisms centered on GABA levels in MT+ region (a sensory cortex) mediate multi-level visuo-spatial component (3D domain) of gF thus drawing a direct connection of biochemistry, brain connectivity, and behavior.

Results

To determine whether the function of hMT+ cortex contributes to visuo-spatial component (3D domain) of gF, we adopted the experimental design depicted in Figure 1b. Thirty-six healthy subjects participated in this study. Participants underwent two MRI sessions: the first encompassing resting-state fMRI and magnetic resonance spectra (MRS), and the second solely involving MRS. A 30-minute interval separated these sessions, during which participants performed motion discrimination tasks (using center-surround antagonism stimuli)(Tadin et al., 2003) and the block design test (BDT), which assesses the visuo-spatial ability (3D domain) of gF(Fangmeier et al., 2006). In the motion discrimination tasks, a grating of either large or small size was randomly presented at the center of the screen. The grating drifted either leftward or rightward, and participants were asked to judge the perceived moving direction. While in the Block design test, participants were asked to rebuild the figural pattern within a specified time limit using a set of red and white blocks. Both the volume-of-interests (VOIs) of MRS scanning in the left hMT+ (targeted brain area) and the left EVC (primarily in V1, control brain area) had dimensions of 2×2×2 cm³, and the MRS scanning sequences were randomized across the two sessions. The hMT+ MRS VOIs were demarcated using an anatomical landmark(Dumoulin et al., 2000). For 14 subjects, we also utilized fMRI to functionally pinpoint the hMT+ to validate the placement of the VOI (Figure 2a, b). The EVC (primarily in V1) MRS VOIs (figure supplement 1) were anatomically defined (Methods). Here, MRS data after extensive quality control (31/36 in hMT+, and 28/36 in EVC (primarily in V1)) were taken for further analysis (Methods).

Figure 2.

Figure supplement 1.

GABA and Glu concentrations in hMT+ and EVC (primarily in V1) and their relation to SI and BDT

An example of a MRS voxel located in hMT+ is shown in Figure 3a. LCModel fittings for GABA spectra from all subjects in hMT+ (n = 31) and EVC (primarily in V1) (n = 28) are illustrated in Figure 3b (color scale presents the BDT scores). We discerned a significant association between the inter-subjects’ BDT scores and the GABA levels in hMT+ voxels, but not in EVC (primarily in V1) voxels. Quantitative analysis displayed that BDT significantly correlates with GABA concentrations in hMT+ voxels (r = 0.39, P = 0.03, n = 31, Figure 3c). After using partial correlation to control for the effect of age, the relationship remains significant (rpartial = 0.426 P = 0.02, 1 participant excluded due to the age greater than mean + 2.5SD) In contrast, there was no obvious correlation between BDT and GABA levels in EVC (primarily in V1) voxels (figure supplement 2a). We show that SI significantly correlates with GABA levels in hMT+ voxels (r = 0.44, P = 0.01, n = 31, Figure 3d). In contrast, no significant correlation between SI and GABA concentrations in EVC (primarily in V1) voxels was observed (figure supplement 2b). This finding is in line with prior results, which indicates that motion perception is associated with neural activity in hMT+ area, but not in EVC (primarily in V1)(Schallmo et al., 2018). LCModel fittings for Glu spectra from all subjects in hMT+ (n = 31) and EVC (primarily in V1) (n = 28) voxels are presented in figure supplement 3a.

Figure 3.

Figure supplement 2.

Figure supplement 3.

Figure supplement 4.

Figure supplement 5.

Unlike in the case of GABA, no significant correlations between BDT and Glu levels were found in both hMT+ and EVC (primarily in V1) voxels (figure supplement 3b, c). While, as expected(Song et al., 2021), we observed significant positive correlations between GABA and Glu concentrations in both hMT+ (r = 0.62, P = 0.0002, n = 31) and EVC (primarily in V1) voxels (r = 0.56, P = 0.002, n = 28) (figure supplement 4a, b). Additionally, significant correlations between SI and BDT, duration threshold of small grating and BDT was discerned (r = 0.59, P = 0.0002, n = 34, Figure 3e, rpartial = 0.67, P < 0.001, 1 participant excluded due to the age greater than mean + 2.5SD; r = - 0.43, P = 0.016, rpartial = 0.44, P = 0.014, Figure 3f). While there was no significant correlation between duration threshold of large grating and BDT (Figure 3g), corroborating previous conclusions(Melnick et al., 2013). Two outliers evident in Figure 3e were excluded, with consistent results depicted in figure supplement 5a. Further, two outliers evident in Figure 3d were excluded, with consistent results depicted in figure supplement 5b.

MT - frontal FC relates to SI and BDT

We next took the left hMT+ as the seed region and separately measured interregional FCs between the seed region and each voxel in the frontal regions (a priori search space). These measurements were correlated with performance in 3D visuospatial ability (BDT) to identify FCs with significant correlations. Results from connectivity-BDT analysis are summarized in Table 1 and shown in Figure 4a. We found that brain regions with FC strength to the seed region (left hMT+) significantly correlated with BDT scores were situated within the canonical cognitive cores of FPN (Brodmann areas (BAs) 6, 9, 10, 46, 47)(Assem et al., 2020; Deary et al., 2010; Duncan et al., 2020; Duncan et al., 2000; Gray et al., 2003; Jung & Haier, 2007). Across the whole brain search, the similar FCs (between hMT+ and frontal cognitive cores) still showed significant correlations with BDT scores (Table supplement 1) (also shown in figure supplement 6a). Additionally, we identified certain parietal regions (BAs 7, 39, 40) with significant correlations between their connectivity to the left hMT+ and the BDT scores (Table supplement 1) (also shown in figure supplement 6a). These significant connections between hMT+ and FPN system suggest that left hMT+ is involved in the efficient information integration network mediating the visuo spatial component of gF.

Table 1

Table supplementary 1.

Table supplement 2.

Table supplement 3.

Figure 4.

Figure supplement 6.

Figure supplement 7.

To address the question whether spatial suppression plays a role, we correlated hMT+ - based global FCs with SI. Though spatial suppression during motion perception (quantified by SI) is considered to be the function of area hMT+(Gautama & Van Hulle, 2001), the top-down modulation from the frontal cortex can increase surround suppression(Liu et al., 2016). Our functional connectivity-SI analysis in the frontal regions (a priori search space) displayed 3 brain regions in which FCs strength significantly correlated with SI: right BA4/6, left BA6, and right BA46 (summarized in Table supplement 2, and shown in Figure 4b). Across the whole brain search, we identified total 7 brain regions in which FCs strength significantly correlated with SI, and 3 of these were in the frontal cortex. This is consistent with the results obtained by the functional connectivity-SI analysis in a priori search space (frontal cortex) (Table supplement 3 and figure supplement 6b).

We also did the V1 functional connectivity-BDT correlations as control analysis (figure supplement 7). Only positive correlations in the frontal area were detected, suggesting that in the 3D visuo-spatial intelligence task, V1 plays a role in feedforward information processing. However, hMT+, which showed specific negative correlations in the frontal, be suggested involving in the inhibition mechanism. These results further emphasize the de-redundancy function of hMT+ in 3D visuo-spatial intelligence.

Local hMT+ GABA acts on SI and BDT via global hMT-frontal connectivity

To determine whether local neurotransmitter levels (such as GABA and Glu) in the hMT+ region mediate the broader 3D visuo-spatial ability of BDT, which as a component of gF, is linked to the frontal cortex(Fangmeier et al., 2006), we correlated the significant FCs of hMT – frontal in Figure 4a (also shown in Table 1) with the GABA and Glu levels in hMT+ region. The results revealed that only two FCs significantly correlated with inhibitory GABA levels in hMT+: 1) the FC of left hMT+- right BA 46 (significantly negative correlation, r = - 0.56, P = 0.02, n = 29, FDR correction, Figure 5a left); 2) the FC of left hMT+ - right BA 6 (significantly positive correlation, r = 0.69, P = 0.002, n = 29, FDR correction, Figure 5b left) (also shown in Table 2). There were no significant correlations between these FCs and the excitatory Glu levels in hMT+ (Table 2). Across the whole brain search, we obtained the same two hMT+ - frontal FCs significantly correlating with both hMT+ GABA levels and BDT (Table supplement 4), this is consistent with the results in the priori search space (frontal cortex) (Table 2). We then correlated the significant FCs in Figure 5b (also in Table supplement 2) with GABA and Glu concentrations in hMT+ and found that almost all the correlations are significant except one (between the FC of left hMT+ - right BA46 and the Glu levels in hMT+) (Table supplement 5). Among the three FCs, the clusters of two FCs have substantial voxel overlap with the FCs we found by the connectivity-BDT analysis (Figure 5a, b). Across the whole brain search, there were total 7 brain regions in which FCs strength were significantly correlated with SI, all the 7 FCs significantly correlated the hMT+ GABA levels, while, no FC had significant correlation with the hMT+ Glu levels (Table supplement 6).

Table 2.

Table supplement 4.

Table supplement 5.

Table supplement 6.

Figure 5.

Figure supplement 8.

Figure Supplement 9.

Taken together, our results displayed that the overlap FCs from the analyses of connectivity - behavior (BDT and SI) -GABA are the hMT+ - BA 46 and hMT+ - BA 6 (Figure 5a, b). These results suggest that the coupling of FCs of hMT+ - frontal regions (BA 46 and BA 6) coupling with local hMT+ GABA provides the neural basis for both the simple motion perception (quantified by SI) and the complex 3D visuo- spatial ability (quantified by BDT).

In order to fully investigate the potential roles of the multiples variables contributing to BDT scores, serial mediation analyses(Hayes, 2013) were applied to both the MR and behavioral data. Following our hypothesis, the independent variable (X) is hMT+ GABA, the dependent variable (Y) is BDT scores, the covariate is the age, and the mediators are FC (M1) and SI (M2). We used the overlap clusters from the analyses of connectivity-BDT-GABA and connectivity-SI-GABA to compute the FC of hMT+ - BA46, 1 participant was excluded due to his age greater than mean + 2.5SD. The serial mediation model is shown in Figure 5c. GABA levels in hMT+ significantly negatively correlated with the FC of hMT+ - BA46 (β = - 0.32, P = 0.0009), which in turn significantly negatively correlated with SI (β = - 0.19, P = 0.035), and consequently, significantly positively correlated with BDT (β = 38.5, P = 0.009). Critically, bootstrapped analyses revealed that our hypothesized indirect effect (i.e., hMT+ GABA → FC of hMT+ - BA46 → SI → BDT) was significant (β = 2.28, SE = 1.54, 95% CI = [0.03, 5.94]). The model accounted for 34% of the variance in BDT. However, when considering the hMT-BA6 FC as the mediator M1, the serial model does not show a significant indirect effect. Consequently, we explored a mediation model, which revealed that the hMT-BA6 FC totally mediates the relationship between GABA and BDS. (Figure 5d). For sensitivity purposes, we tested the alternative models, in which the order of the mediators was reversed. The pathway that hMT+ GABA was predicted to be associated with SI, followed by the FC of hMT+ - BA 46, and then BDT, did not yield the chained mediation effects on BDT (figure supplement 8).

To summarize (shown in Figure 6), the results from the serial mediation analyses are consistent with our hypothesis. That is, higher GABAergic inhibition in hMT+ relates to stronger negative FC between hMT+ and BA46, leading to enhanced ability for surround suppression (filtering out irrelevant information(Tadin, 2015), which ultimately resulting in more efficient visual 3D processing as key component of gF (the higher BDT scores).

Figure 6.

Discussion

Here, we provide evidence that hMT+ inhibitory mechanisms mediate processing in the visuo-spatial component (3D domain) of gF on multiple levels, that is, from molecular over brain connectivity to behavior. First, this study found that higher hMT+ inhibitory GABA levels (but not excitatory Glu) relate to FC between hMT+ and BA 46 that contribute to both SI and BDT. Our serial mediation analyses indicate that the inhibitory mechanisms related to hMT+ and its GABA levels in hMT+ (but not Glu), FCs of hMT+ - BA46 coupling with hMT+ inhibitory GABA (but not excitatory Glu), and behavior (SI indexing perceptual suppression in hMT+) predict the inter-subject variance in the 3D gF task (BDT) (Figure 5c). Second, we demonstrate discrete GABAergic inhibition mechanisms in hMT+ that mediate the strong FCs between hMT+ - frontal regions (BA46 and BA6): significant negative correlation with the FC of hMT+ - BA 46 (Figure 5a), whereas there is significant positive correlation with the FC of hMT+ - BA 6 (Figure 5b). This indicates that different frontal regions, DLPFC (BA 46) and premotor cortex (BA6), contribute uniquely to gF through hMT+ - based inhibitory mechanisms.

The goal of our research is to reveal that the inhibitory (not excitatory) mechanism in hMT+ contributes to multi-level processing in 3D visuo-spatial ability (BDT). Monkey electrophysiological experiments revealed that selective attention gates the visual cortex, including area MT, effectively suppressing the irrelevant information(Everling et al., 2002; Treue & Maunsell, 1996). These findings align with the “neural efficiency” hypothesis of intelligence(Haier et al., 1988), which puts forward the human brain’s ability to suppress the repetition of information. Neural suppression is associated with the balance between excitation and inhibition (EIB), usually represented by covariation between Glutamate and GABA(Ozeki et al., 2009). Here, this study exploited the high spectral resolution afforded by ultrahigh field (7T) MRS to reliably resolve GABA measurement, to adequately discriminate the glutamate and glutamine signals, and to resolve the high accuracy Glu measurement(Ende, 2015). This work implemented the MRS scanning in hMT+ (3D visual domain) and EVC (primarily in V1) (2D visual domain) regions and found that hMT+ inhibitory GABA (but not excitatory Glu) significantly correlated with BDT, i.e., the higher GABA levels in hMT+ (rather than excitatory Glu) relate to higher visual 3D processing (BDT) (Figure 3c). Basically, this study contains the data of SI, BDT, GABA in MT+ and EVC (primarily in V1), Glu in MT+ and EVC (primarily in V1)-all 6 measurements. we made a correlation matrix to reporting all values in figure supplementary 9.

We searched the global hMT+ - based FCs with the connectivity-BDT analyses (in priori search space and whole brain search to valid), and then, correlated these significant FCs with the GABA and Glu concentrations in hMT+. We found two FCs (hMT+ - BA46 and hMT+ - BA6) significantly correlating with hMT+ inhibitory GABA (whereas no FC significantly correlated with hMT+ excitatory Glu). Accordingly, our results emphasize the importance of hMT+ inhibitory GABA (but not excitatory Glu) in processing the 3D visual-spatial intelligence (BDT).

Our recent human study(Song et al., 2021) and other study’s animal experiments(Ozeki et al., 2009; Sato et al., 2016) demonstrated that the conjoint action of inhibition (GABA) and excitation (Glu) underlies visual spatial suppression. In this work, our novel data show the chained mediation effects from local hMT+ GABA to more global BDT: hMT+ GABA → FC (hMT+ and BA46) → SI → BDT. Thereby, our data indicate that inhibitory mechanisms in hMT+, from the biochemical level of GABA over FC to the behavioral level, can predict the inter-subject variance in the 3D gF task (BDT) (Figure 5c).

Another interesting finding reveal that GABAergic inhibition in hMT+ coupling with distinct functional connectivity patterns between BA 46-hMT+ and BA6-hMT+. A previous human fMRI experiment found that the positive and negative correlations between BDT and the activation of frontal regions appeared at different reasoning phases (validation or integration phases during reasoning)(Fangmeier et al., 2006). On the one hand, a monkey electrophysiological experiment reported the delayed modulation from PFC (especially in DLPFC (BA 46))) to area MT during a visual motion task(Zaksas & Pasternak, 2006). Computational models converged with empirical data of awake monkey experiments slowing temporal modulation from PFC to MT/MST(Donner et al., 2009; Siegel et al., 2015; Wang, 2002; Wimmer et al., 2015). On the other hand, human MEG studies(Donner et al., 2009; Wilming et al., 2020) reported that the gamma-band activity in the visual cortex (including area MT) exhibited high coherence with the activity in (pre-) motor regions (BA 4/6). These results suggest that the relation of long-range FC and local inhibitory mechanism (hMT+ GABA) support our findings that inhibition in hMT+ contributes to efficient long-range integration and coordination in distant brain areas like the prefrontal and premotor cortex.

How does hMT+ assemble into the MD system as an intellectual hub rather than a simple input module? The results in Figure 5a, b showed that the overlap brain regions from the analyses of connectivity-BDT-GABA/connectivity-SI-GABA are the hMT+ - BA 46. This overlap couples with local visual suppression (SI) and consequently plays an important role in intelligence (BDT). The direction discrimination task in this work (the visual motion paradigm of center-surround antagonism) was previously considered a mainly local function of hMT+(Melnick et al., 2013; Tadin, 2015; Tadin et al., 2003). However, our results with connectivity-SI analyses revealed that both local (FC within BA 18) and global brain connectivity (FC between hMT+ and frontal regions) contribute to SI (Table supplement 3). In human psychophysical experiments(Melnick et al., 2013; Tadin et al., 2003) the brief stimulus duration (∼100 ms) in motion discrimination precludes most top-down attentional effects(Wang, 2002; Zaksas & Pasternak, 2006), while, attention, which predicted the performance of the motion discrimination task, was sustained throughout the stimulus intervals(Siegel et al., 2015). Furthermore, animal experiments have revealed that the local circuits in the visual cortex combining with top-down modulation and intracortical horizontal connection mediate the visual-spatial suppression(Angelucci et al., 2002; Keller et al., 2020; Li et al., 2019; Zhang et al., 2014).

Our results (shown in Figure 5a, b, right) present the intrinsic binding of local GABAergic inhibition in hMT+, which suppressing redundancy of visual motion processing (SI), and the activity of brain connectivity between hMT+ and frontal regions. These individually inherent traits may contribute to the individual difference in 3D visuo-spatial ability (Figure 5a, b, left). A candidate divisive normalization model(Carandini & Heeger, 2011; Reynolds & Heeger, 2009) can explain how such reverberation affects the process of suppressing the irrelevant information, from perception to intelligence(Melnick et al., 2013; Tadin, 2015). We summarize a framework (Figure 6) to indicate and visualize our findings.

Recently, Duncan et al. demonstrated coding of general fluid intelligence (gF) in distributed regions, defining them as part of multi-demand (MD) systems (Assem et al., 2020; Duncan et al., 2020). The MD system encompasses a range of cognitive domains, including working memory, mathematics, language, and relational reasoning. According to Melnick et al. (2013), motion surround suppression (SI) and time thresholds for small and large gratings, which reflect hMT+ functionality, are correlated with Verbal Comprehension, Perceptual Reasoning, Working Memory, and Processing Speed indicators. Additionally, Fedorenko et al. identified multi-demand activation regions around the occipito-temporal areas, potentially overlapping with hMT+ (Fedorenko et al., 2013). As a key region in the representation of sensory flows (including optic, and auditory flows)(Fetsch et al., 2011; Gu et al., 2006), hMT+ shows potential to be central to the MD system. Future research could focus on multi-task paradigms to further investigate the mechanisms of hMT+ and its relationship with broader cognitive functions.

Together, this study offers a comprehensive insight into how the information exchange and integration between the sensory cortex (hMT+) and cognition core of BA 46, coupling with the hMT+ GABA, can predict the performance of 3D visuo-spatial ability (BDT). Our results provide direct evidence that a sensory cortex area (hMT+), its GABA biochemistry, functional connectivity, and cognition behavior levels, can assemble into complex cognition as an intellectual hub.

Materials and Methods

Subjects

Thirty-six healthy subjects (18 female, mean age: 23.6 years±2.1, range: 20 to 29 years) participated in this study, they were recruited from Zhejiang University. All subjects had normal or corrected-to-normal vision. In addition, they reported no psychotropic medication use, no illicit drug use within the past month, no alcohol use within 3 days prior to scanning, and right-handed. This experiment was approved by the Ethics Review Committee of Zhejiang University and conducted in accordance with the Helsinki Declaration. All participants signed informed consent forms prior to the start of the study and were compensated for their time. All subjects participated in the motion spatial suppression psychophysical, resting-state fMRI and MRS (hMT+ and EVC (primarily in V1) regions, in random sequence) experiments, but only part of the MRS data (31/36 in hMT+ region and 28/36 in EVC (primarily in V1) region) survived quality control (see the part of MRS date processing). The sample size is determined by the statistic requirement (30 sample for Person correlation statistical analysis).

Motion surrounding suppression measurement

All stimuli were generated using Matlab (MathWorks, Natick, MA) with Psychophysics Toolbox(Brainard, 1997), and were shown on a linearized monitor (1920×1080 resolution, 100-Hz refresh rate, Cambridge Research System, Kent, UK). The viewing distance was 72 cm from the screen, with the head stabilized by a chinrest. Stimuli were drawn against a gray (56 cd per m^-2) background.

A schematic of the stimuli and trial sequences is shown in our recent study(Song et al., 2021). The stimulus was a vertical drifting sinusoidal grating (contrast, 50%; spatial frequency, 1 cycle/°; speed, 4°/s) of either small (diameter of 2°) or large (diameter of 10°) size. The edge of the grating was blurred with a raised cosine function (width, 0.3°). A cross was presented in the center of the screen at the beginning of each trial for 500ms, and participants were instructed to fixate at the cross and to keep fixating at the cross throughout the trial. In each trial, a grating of either large or small size was randomly presented at the center of the screen. The grating drifted either leftward or rightward, and participants were asked to judge the perceived moving direction by a key press. Response time was not limited. The grating was ramped on and off with a Gaussian temporal envelope, and the grating duration was defined as 1 SD of the Gaussian function. The duration was adaptively adjusted in each trial, and duration thresholds were estimated by a staircase procedure. Thresholds for large and small gratings were obtained from a 160-trial block that contained four interleaved 3-down/1-up staircases. For each participant, we computed the correct rate for different stimulus durations separately for each stimulus size. These values were then fitted to a cumulative Gaussian function, and the duration threshold corresponding to the 75% correct point on the psychometric function was estimated for each stimulus size.

Stimulus demonstration and practice trials were presented before the first run. Auditory feedback was provided for each wrong response. To quantify the spatial suppression strength, we calculated the spatial suppression index (SI), defined as the difference of log10 thresholds for large versus small stimuli(Schallmo et al., 2018; Tadin et al., 2003):

Block design task measurement

The block design task was administered in accordance with the WAIS-IV manual(Wechsler, 2008). Specifically, participants were asked to rebuild the figural pattern within a specified time limit using a set of red and white blocks. The time limits were set as 30 s to 120 s according to different levels of difficulty. The patters were presented in ascending order of difficulty, and the test stopped if two consecutive patterns were not constructed in the allotted time. The score was determined by the accomplishment of the pattern and the time taken. A time bonus was awarded for rapid performance in the last six patterns. The score ranges between 0 and 66 points, with higher scores indicating better perceptual reasoning.

MR experimental procedure

MR experiments were performed in a 7T whole body MR system (Siemens Healthcare, Erlangen, Germany) with a Nova Medical 32 channel array head coil. Sessions included resting-state functional MRI, fMRI localizer scan, structural image scanning, and MRS scan. Resting-state scans were acquired with 1.5-mm isotropic resolution (transverse orientation, TR/TE = 2000/20.6 ms, 160 volumes, slice number = 90, flip angle = 70°, eyes closed). Structural images were acquired using a MP2RAGE sequence (TR/ TI1/ TI2 = 5000/901/3200 ms) with 0.7-mm isotropic resolution. MRS data were collected within two regions (hMT+ and EVC (primarily in V1)) for each subject, and we divided them into two sessions to avoid discomfort caused by long scanning. The order of MRS VOIs (hMT+ and EVC (primarily in V1)) in the two sessions was counterbalanced across participants. Interval between two sessions was used for block design and motion discrimination tasks. One session included fMRI localizer scan, structural image scanning, and MRS scan for the hMT+ region; the other session included structural image scan, and MRS scan for the EVC (primarily in V1) region. Spectroscopy data were acquired using a ¹H-MRS single-voxel short-TE STEAM (Stimulated Echo Acquisition Mode) sequence(Frahm et al., 1989) (TE/TM/TR = 6/32/7100ms) with 4096 sampling points, 4-kHz bandwidth, 16 averages, 8 repetitions, 20×20×20 mm³ VOI size, and VAPOR (variable power and optimized relaxation delays) water suppression(Tkáč et al., 1999). Prior to acquisition, first- and second-order shims were adjusted using FASTMAP (fast, automatic shimming technique by mapping along projections(Gruetter, 1993). Two non-suppressed water spectra were also acquired: one for phase and eddy current correction (only RF pulse, 4 averages) and another for metabolite quantification (VAPOR none, 4 averages). Voxels were positioned based on anatomical landmarks using a structural image scan collected in the same session, while avoiding contamination by CSF, bone, and fat. The hMT+ VOIs were placed in the ventrolateral occipital lobe, which was based on anatomical landmarks(Dumoulin et al., 2000; Schallmo et al., 2018). We did not distinguish between the middle temporal (MT) and medial superior temporal (MST) areas in these hMT+ VOIs(Huk et al., 2002). For 14 subjects, we also functionally identified hMT+ as a check on the placement of the VOI. A protocol was used with a drifting grating (15% contrast) alternated with a static grating across blocks (10 s block duration, 160 TRs total). Using fMRI BOLD signals, these localizer data were processed online to identify the hMT+ voxels in the lateral occipital cortex, which responded more strongly to moving vs. static gratings. In addition, we only used the left hMT+ as the target region to scan, which was motivated by studies showing that left hMT+ was more effective at causing perceptual effects(Tadin et al., 2011). For EVC (primarily in V1) region, the VOI was positioned on each subject’s calcarine sulcus on the left side(Tadin et al., 2011) based on anatomical landmarks(Boucard et al., 2007; Dumoulin et al., 2000)

MRS data processing

Spectroscopy data were preprocessed and quantified using magnetic resonance signal processing and analysis, https://www.cmrr.umn.edu/ downloads/mrspa/), which runs under MATLAB and invokes the interface of the LCModel (Version 6.3-1L) (Chen et al., 2019). First, we used the non-suppressed water spectra to perform eddy current correction and frequency/phase correction. Second, we checked the quality of each FID (16 averages) visually and removed those with obviously poor quality. Third, the absolute concentrations of each metabolite were quantitatively estimated via the Water- Scaling method. For partial-volume correction, the tissue water content was computed as follows(Ernst et al., 1993):

where fgm, fwm, and fcsf were the GM/WM/CSF volume fraction in MRS VOI and we used FAST (fMRI’s automated segmentation tool, part of the FSL toolbox)(Zhang et al., 2001) to segment the three tissue compartments from the T1-weighted structural brain images. For water T2 correction, we set water T2 as 47ms (Marjańska et al., 2012). Our concentrations were mM per kg wet weight. Furthermore, LCModel analysis was performed on all spectra within the chemical shift range of 0.2 to 4.0 ppm.

Poor spectral quality was established by a Cramer-Rao Lower Bound (CRLB) of more than 20%(Cavassila et al., 2001), and some data were excluded from further analysis. The details were described in our recently paper(Song et al., 2021).

Rs-fMRI data processing and analysis

Resting-state functional image was analyzed in the Data Processing and Analysis for Brain Imaging DPABI toolbox(Yan et al., 2016) based on SPM 12 (http://www.fil.ion.ucl.ac.uk/spm/). The preprocessing steps included discard of the first five volumes, slice timing, realignment to the 90th slice, coregistration of each subject’s T1-weighted anatomical and functional images, segmentation of the anatomical images into six types of tissues using DARTEL, linear detrend, regressing nuisance variables (including realignment Friston 24-parameter, global signal, white matter and CSF signal) (Friston et al., 1996), normalization to the standard Montreal Neurological Institute (MNI) space with the voxel size of 1.5× 1.5× 1.5 mm³ using DARTEL, spatial smoothing with a Gaussian kernel of 3 mm full-width-half-maximum (FWHM), and band-pass filtering with Standard frequency band (SFB, 0.01–0.1 Hz). Spherical ROI with a radius of 6mm was placed in left MT. The coordinate for left MT (-46, -72, -4, in MNI space) was obtained by our localizer fMRI experiment. We calculated the seed-to-voxel whole brain FC map for each subject. All the FC values were Fisher-Z-transformed.

We did a similar connectivity-behavior analysis to a previous study (Song et al., 2008). First, we computed the Pearson’s correlation coefficient between BDT scores and the FC values across subjects in a voxel-based way. Then, to evaluate the significance, we transformed the r-value into t-value , where df denotes to the degrees of freedom, and r is the Pearson’s correlation coefficient between BDT scores and the FC values. Here, df was equal to 27. The brain regions in which the FC values to the seed region was significantly correlated with the BDT scores were obtained with a threshold of P < 0.005 for regions of a priori (|t₍₂₇₎ | ≥ 3.057, and adjacent cluster size ≥ 23 voxels (AlphaSim corrected)), and P < 0.01 for whole-brain analyses (|t₍₂₇₎ | ≥ 2.771 and adjacent cluster size ≥ 37 voxels (AlphaSim corrected).

Statistical Analysis

PROCESS version 3.4, a toolbox in SPSS, was used to examine the mediation model. There are some prerequisites for mediation analysis: the independent variable should be a significant predictor of the mediator, and the mediator should be a significant predictor of the dependent variable.

SPSS 20 (IBM, USA) was used to conduct all the remaining statistical analysis in the study. We evaluated the correlation of variables (GABA, Glu, SI, BDT) using Pearson’s correlation analysis. Differences or correlations were considered statistically significant if P < 0.05. Significances with multiple comparisons were tested with false discovery rate (FDR) correction. The effect of age on intelligence was controlled for by using partial correlation in the correlation analysis and was taken as a covariate in the serial mediation model analysis.

Data availability

Source data are provided with this paper and have been archived at zenodo and could be downloaded with reasonable request, https://doi.org/10.5281/zenodo.12789781

Code availability

This code has been uploaded to the GitHub: https://github.com/Yrehearsal/GABA-_hMT-_Intelligence

Acknowledgements

The authors thank Prof. Dost Ongur and Fei Du for guidance on the MRS data processing. Thank Prof. Xinyi Lai for supporting MRI data acquisition. Thank Guohua Xu and Fen Yang for technical assistance. This work was supported by STI 2030—Major Projects (2021ZD0200401 to X.M.S., 2022ZD0206000 to R.B.), the National

Natural Science Foundation of China Grants (U1909205, 61876222, 32000761, 82222032), Humanities and Social Sciences Ministry of Education (20YJC880095, 18YJA190001), the Key R&D Program of Zhejiang (2022C03096 to X.M.S., 2022ZJJH02-06 to G.C.), the European Union’s Horizon 2020 Framework Program for Research and Innovation under the Specific Grant Agreement No. 785907 (Human Brain Project SGA2 to G.N.), and the MOE Frontier Science Center for Brain Science & Brain- Machine Integration, Zhejiang University.

Author contributions

S.X.M. and Y.G. designed the experiment and G.N. guided the logic of the analysis.

Y.G., Y.C. and D.L. conducted human experiments, analyzed data, and Y.G. created figures. R.B. guided the MRI experiments. J.Y., J.W. and B.X. were in charge of data collection and partial date analysis. T. W., M.L. and G.C. guided the data analysis. S.X.M., Y.G. and G.N. wrote the manuscript.

Competing interests

The authors declare no competing interests.