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Regional inactivations of primate ventral prefrontal cortex reveal two distinct mechanisms underlying negative bias in decision making.


Type

Article

Change log

Authors

Clarke, Hannah F 
Horst, Nicole K 
Roberts, Angela C 

Abstract

Dysregulation of the orbitofrontal and ventrolateral prefrontal cortices is implicated in anxiety and mood disorders, but the specific contributions of each region are unknown, including how they gate the impact of threat on decision making. To address this, the effects of GABAergic inactivation of these regions were studied in marmoset monkeys performing an instrumental approach-avoidance decision-making task that is sensitive to changes in anxiety. Inactivation of either region induced a negative bias away from punishment that could be ameliorated with anxiolytic treatment. However, whereas the effects of ventrolateral prefrontal cortex inactivation on punishment avoidance were seen immediately, those of orbitofrontal cortex inactivation were delayed and their expression was dependent upon an amygdala-anterior hippocampal circuit. We propose that these negative biases result from deficits in attentional control and punishment prediction, respectively, and that they provide the basis for understanding how distinct regional prefrontal dysregulation contributes to the heterogeneity of anxiety disorders with implications for cognitive-behavioral treatment strategies.

Description

Keywords

anxiety, negative bias, orbitofrontal cortex, ventrolateral prefrontal cortex, Amygdala, Animals, Anti-Anxiety Agents, Anxiety Disorders, Attention, Behavior, Animal, Bias, Callithrix, Decision Making, Female, Hippocampus, Magnetic Resonance Imaging, Male, Neuroimaging, Prefrontal Cortex, Vision, Ocular

Journal Title

Proc Natl Acad Sci U S A

Conference Name

Journal ISSN

0027-8424
1091-6490

Volume Title

112

Publisher

Proceedings of the National Academy of Sciences
Sponsorship
Medical Research Council (G1000183)
Medical Research Council (G0901884)
Medical Research Council (G0001354)
Medical Research Council (G1100307)
Medical Research Council (MR/M023990/1)
Wellcome Trust (093875/Z/10/Z)
All authors contributed extensively to the work presented in this article, and we thank Rudolf Cardinal for helpful advice and discussion and Mercedes Arroyo for histology. This research was funded by a Medical Research Council Programme Grant (to A.C.R.) and Career Development Award (to H.F.C.). The research was conducted at the Behavioural and Clinical Neuroscience Institute, which is supported by a joint award from the Medical Research Council and Wellcome Trust (G00001354).