Circuit mechanisms for the chemical modulation of cortex-wide network interactions and behavioral variability

Thomas Pfeffer, Adrian Ponce-Alvarez, Konstantinos Tsetsos, Thomas Meindertsma, Christoffer Julius Gahnström, Ruud Lucas van den Brink, Guido Nolte, Andreas Karl Engel, Gustavo Deco, Tobias Hinrich Donner

Research output: Contribution to journalArticle (Academic Journal)peer-review

Abstract

Influential theories postulate distinct roles of catecholamines and acetylcholine in cognition and behavior. However, previous physiological work reported similar effects of these neuromodulators on the response properties (specifically, the gain) of individual cortical neurons. Here, we show a double dissociation between the effects of catecholamines and acetylcholine at the level of large-scale interactions between cortical areas in humans. A pharmacological boost of catecholamine levels increased cortex-wide interactions during a visual task, but not rest. An acetylcholine boost decreased interactions during rest, but not task. Cortical circuit modeling explained this dissociation by differential changes in two circuit properties: the local excitation-inhibition balance (more strongly increased by catecholamines) and intracortical transmission (more strongly reduced by acetylcholine). The inferred catecholaminergic mechanism also predicted noisier decision-making, which we confirmed for both perceptual and value-based choice behavior. Our work highlights specific circuit mechanisms for shaping cortical network interactions and behavioral variability by key neuromodulatory systems.

Original languageEnglish
Article numbereabf5620
JournalScience Advances
Volume7
Issue number29
Early online date16 Jul 2021
DOIs
Publication statusPublished - Jul 2021

Bibliographical note

Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

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