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Lesions of either anterior orbitofrontal cortex or ventrolateral prefrontal cortex in marmoset monkeys heighten innate fear and attenuate active coping behaviors to predator threat.


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Authors

Shiba, Yoshiro 
Kim, Charissa 
Santangelo, Andrea M 
Roberts, Angela C 

Abstract

The ventral prefrontal cortex is an integral part of the neural circuitry that is dysregulated in mood and anxiety disorders. However, the contribution of its distinct sub-regions to the regulation of negative emotion are poorly understood. Recently we implicated both the ventrolateral prefrontal cortex (vlPFC) and anterior orbitofrontal cortex (antOFC) in the regulation of conditioned fear and anxiety responses to a social stimulus, i.e., human intruder, in the marmoset monkey. In the present study we extend our investigations to determine the role of these two regions in regulating innate responses and coping strategies to a predator stimulus, i.e., a model snake. Both the vlPFC and antOFC lesioned groups exhibited enhanced anxiety-related responses to the snake in comparison to controls. Both groups also showed a reduction in active coping behavior. These results indicate that the vlPFC and antOFC contribute independently to the regulation of both innate fear and, as previously reported, conditioned fear, and highlight the importance of these regions in producing stimulus-appropriate coping responses. The finding that dysregulation in two distinct prefrontal regions produces the apparently similar behavioral phenotype of heightened negative emotion provides insight into the varied etiology that may underlie this symptom across a wide variety of neuropsychiatric conditions with implications for personalized treatment strategies.

Description

Keywords

anxiety, emotion regulation, prefrontal cortex, primate, snake fear

Journal Title

Front Syst Neurosci

Conference Name

Journal ISSN

1662-5137
1662-5137

Volume Title

8

Publisher

Frontiers Media SA
Sponsorship
Medical Research Council (G1000183)
Medical Research Council (G0901884)
Medical Research Council (G0001354)
Wellcome Trust (093875/Z/10/Z)
This research was supported by a Medical Research Programme Grant (G0901884) from the Medical Research Council (MRC), UK to Angela C. Roberts. Yoshiro Shiba was supported by the Long Term Student Support Program provided by Osaka University and the Ministry of Education, Culture, Sports, Science and Technology of Japan and currently by the MRC Programme grant (G0901884). Andrea M. Santangelo, until October 2011, by a J. S. McDonnell Foundation grant (Principle Investigators; E. Phelps, T. W. Robbins, co-investigators; J. E. LeDoux, and Angela C. Roberts) and currently by the MRC Programme grant (G0901884). Work was carried out within the Behavioral and Clinical Neurosciences Institute supported by a consortium award from the Wellcome Trust and the MRC. We thank Dr. Carmen Agustín-Pavón for conducting the lesion surgeries, Dr. Katrin Braesicke for help with statistical analyses and Dr. Mercedes Arroyo for the preparation of histological material.