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Dynamic Subcortical Modulators of Human Default Mode Network Function

Ben J. Harrison, Christopher G. Davey, Hannah S. Savage, Alec J. Jamieson, Christine A. Leonards, Bradford A. Moffat, Rebecca K. Glarin, Trevor Steward

preprint DOI: 10.1101/2021.10.27.466172 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Functional magnetic resonance imaging study
Population Human participants undergoing functional MRI
Topics Default mode network
Key points The basal forebrain showed activity suppression with DMN cortical regions during rest-to-external-task transitions and, per dynamic causal modelling, drove changes in DMN cortical activity. The mediodorsal thalamus was engaged during internally focused cognition and exerted a broad excitatory influence on DMN cortical activation. The authors present this as the first direct human evidence of distinct basal forebrain and thalamic influences on DMN function.

Abstract

Abstract: The brain’s ‘default mode network’ (DMN) enables flexible switching between internally and externally focused cognition. Precisely how this modulation occurs is not well understood, although may involve key subcortical mechanisms, including hypothesized influences from the basal forebrain (BF) and mediodorsal thalamus (MD). Here, we used ultra-high field (7T) functional magnetic resonance imaging to examine the involvement of the BF and MD across states of task-induced DMN activity modulation. Specifically, we mapped DMN activity suppression (‘deactivation’) when participants transitioned between rest and externally focused task performance, as well as DMN activity engagement (‘activation’) when task performance was internally (i.e., self) focused. Consistent with recent rodent studies, the BF showed overall activity suppression with DMN cortical regions when comparing the rest to external task conditions. Further analyses, including dynamic causal modelling, confirmed that the BF drove changes in DMN cortical activity during these rest-to-task transitions. The MD, by comparison, was specifically engaged during internally focused cognition and demonstrated a broad excitatory influence on DMN cortical activation. These results provide the first direct evidence in humans of distinct basal forebrain and thalamic circuit influences on the control of DMN function and suggest novel mechanistic avenues for ongoing translational research.

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