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. 2023 Oct 13:3:kkad016.
doi: 10.1093/psyrad/kkad016. eCollection 2023.

The right inferior frontal gyrus as pivotal node and effective regulator of the basal ganglia-thalamocortical response inhibition circuit

Affiliations

The right inferior frontal gyrus as pivotal node and effective regulator of the basal ganglia-thalamocortical response inhibition circuit

Qian Zhuang et al. Psychoradiology. .

Abstract

Background: The involvement of specific basal ganglia-thalamocortical circuits in response inhibition has been extensively mapped in animal models. However, the pivotal nodes and directed causal regulation within this inhibitory circuit in humans remains controversial.

Objective: The main aim of the present study was to determine the causal information flow and critical nodes in the basal ganglia-thalamocortical inhibitory circuits and also to examine whether these are modulated by biological factors (i.e. sex) and behavioral performance.

Methods: Here, we capitalize on the recent progress in robust and biologically plausible directed causal modeling (DCM-PEB) and a large response inhibition dataset (n = 250) acquired with concomitant functional magnetic resonance imaging to determine key nodes, their causal regulation and modulation via biological variables (sex) and inhibitory performance in the inhibitory circuit encompassing the right inferior frontal gyrus (rIFG), caudate nucleus (rCau), globus pallidum (rGP), and thalamus (rThal).

Results: The entire neural circuit exhibited high intrinsic connectivity and response inhibition critically increased causal projections from the rIFG to both rCau and rThal. Direct comparison further demonstrated that response inhibition induced an increasing rIFG inflow and increased the causal regulation of this region over the rCau and rThal. In addition, sex and performance influenced the functional architecture of the regulatory circuits such that women displayed increased rThal self-inhibition and decreased rThal to GP modulation, while better inhibitory performance was associated with stronger rThal to rIFG communication. Furthermore, control analyses did not reveal a similar key communication in a left lateralized model.

Conclusions: Together, these findings indicate a pivotal role of the rIFG as input and causal regulator of subcortical response inhibition nodes.

Keywords: DCM; basal ganglia; effective connectivity; inferior frontal gyrus; response inhibition.

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Conflict of interest statement

K.M.K. holds the position of Editor-in-Chief and B.B. is a member of editorial board of Psychoradiology. They were blinded from the review process and making decisions on the manuscript. Disclaimer: Any opinions, findings, conclusions or recommendations expressed in this publication do not reflect the views of the Government of the Hong Kong Special Administrative Region or the Innovation and Technology Commission.

Figures

Figure 1:
Figure 1:
Brain activation maps for general response inhibition on whole brain level (contrast: NoGo > Go; P < 0.05 FWE, peak level). L, left; R, right. The color bar represents the t-values of the BOLD signal and reflect the significance level of the contrast.
Figure 2:
Figure 2:
Location of regions included in the right model and group-level connectivity parameters. (A) Location of regions included in the right model. The A matrix: intrinsic connectivity across all experimental conditions (B, F). The B matrix: modulatory effect on effective connectivity between regions and self-inhibitions from NoGo (C, G) and Go condition (D, H). The C matrix: Driving inputs in ROI in the NoGo and Go condition (E, I). Values in matrices reflect the connectivity parameters. Effective connectivity strengths are displayed by the color ranging from yellow to dark red (i.e. excitatory connectivity) and from turquoise to dark blue (i.e. inhibitory). Parameters with stronger evidence (posterior probability >95%) are presented and subthreshold parameters are marked with “n.s.”.
Figure 3:
Figure 3:
Sex effect on connectivity parameters in terms of A matrix and B matrix. (A) For intrinsic connectivity in A matrix, female participants showed a more negative influence from rThal to rGP compared to male participants. (B) In the NoGo condition, there is a greater self-inhibition in rThal in female than male participants in terms of B matrix. Effective connectivity strengths are displayed by the color ranging from yellow to dark red (i.e. excitatory connectivity) and from turquoise to dark blue (i.e. inhibitory). Parameters with stronger evidence (posterior probability > 95%) are presented.
Figure 4:
Figure 4:
Location of regions included in the left model and group-level connectivity parameters. (A) Location of regions included in the left model. The A matrix: intrinsic connectivity independent of experimental conditions (B, F). The B matrix: modulatory effect on effective connectivity between regions and self-connections in the NoGo (C, G) and Go condition (D, H). The C matrix: driving inputs into ROI of NoGo and Go conditions (E, I). Values in matrices reflect the connectivity parameters. Effective connectivity strengths are displayed by the color ranging from yellow to dark red (i.e. excitatory connectivity) and from turquoise to dark blue (i.e. inhibitory). Parameters with stronger evidence (posterior probability > 95%) are presented and subthreshold parameters marked with “n.s.”.

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