Chemogenetics Reveal an Anterior Cingulate–Thalamic Pathway for Attending to Task-Relevant Information. (30th November 2020)

• Record Type: Journal Article
• Authors: Bubb, Emma J; Aggleton, John P; O'Mara, Shane M; Nelson, Andrew J D
• Is Part Of: Cerebral cortex. Volume 31:Number 4(2021)
• Page Start: 2169
• Page End: 2186
• Publication Date: 2020-11-30
• Subjects: anterior cingulate cortex -- anterior thalamic nuclei -- attentional-set formation -- DREADDs -- extradimensional set-shift; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhaa353
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: In a changing environment, organisms need to decide when to select items that resemble previously rewarded stimuli and when it is best to switch to other stimulus types. Here, we used chemogenetic techniques to provide causal evidence that activity in the rodent anterior cingulate cortex and its efferents to the anterior thalamic nuclei modulate the ability to attend to reliable predictors of important outcomes. Rats completed an attentional set-shifting paradigm that first measures the ability to master serial discriminations involving a constant stimulus dimension that reliably predicts reinforcement (intradimensional-shift), followed by the ability to shift attention to a previously irrelevant class of stimuli when reinforcement contingencies change (extradimensional-shift). Chemogenetic disruption of the anterior cingulate cortex (Experiment 1) as well as selective disruption of anterior cingulate efferents to the anterior thalamic nuclei (Experiment 2) impaired intradimensional learning but facilitated 2 sets of extradimensional-shifts. This pattern of results signals the loss of a corticothalamic system for cognitive control that preferentially processes stimuli resembling those previously associated with reward. Previous studies highlight a separate medial prefrontal system that promotes the converse pattern, that is, switching to hitherto inconsistent predictors of reward when contingencies change. Competition between these 2 systems regulates cognitive flexibility and choice.