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Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat
Stress-related disorders such as depression and anxiety are characterized by enhanced negative emotion and physiological dysfunction. Whilst elevated activity within area 25 of the subgenual anterior cingulate cortex (sgACC/25) has been implicated in these illnesses, it is unknown whether this over-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588412/ https://www.ncbi.nlm.nih.gov/pubmed/33106488 http://dx.doi.org/10.1038/s41467-020-19167-0 |
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author | Alexander, Laith Wood, Christian M. Gaskin, Philip L. R. Sawiak, Stephen J. Fryer, Tim D. Hong, Young T. McIver, Lauren Clarke, Hannah F. Roberts, Angela C. |
author_facet | Alexander, Laith Wood, Christian M. Gaskin, Philip L. R. Sawiak, Stephen J. Fryer, Tim D. Hong, Young T. McIver, Lauren Clarke, Hannah F. Roberts, Angela C. |
author_sort | Alexander, Laith |
collection | PubMed |
description | Stress-related disorders such as depression and anxiety are characterized by enhanced negative emotion and physiological dysfunction. Whilst elevated activity within area 25 of the subgenual anterior cingulate cortex (sgACC/25) has been implicated in these illnesses, it is unknown whether this over-activity is causal. By combining targeted intracerebral microinfusions with cardiovascular and behavioral monitoring in marmosets, we show that over-activation of sgACC/25 reduces vagal tone and heart rate variability, alters cortisol dynamics during stress and heightens reactivity to proximal and distal threat. (18)F-FDG PET imaging shows these changes are accompanied by altered activity within a network of brain regions including the amygdala, hypothalamus and dorsolateral prefrontal cortex. Ketamine, shown to have rapid antidepressant effects, fails to reverse elevated arousal to distal threat contrary to the beneficial effects we have previously demonstrated on over-activation induced reward blunting, illustrating the symptom-specificity of its actions. |
format | Online Article Text |
id | pubmed-7588412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75884122020-11-10 Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat Alexander, Laith Wood, Christian M. Gaskin, Philip L. R. Sawiak, Stephen J. Fryer, Tim D. Hong, Young T. McIver, Lauren Clarke, Hannah F. Roberts, Angela C. Nat Commun Article Stress-related disorders such as depression and anxiety are characterized by enhanced negative emotion and physiological dysfunction. Whilst elevated activity within area 25 of the subgenual anterior cingulate cortex (sgACC/25) has been implicated in these illnesses, it is unknown whether this over-activity is causal. By combining targeted intracerebral microinfusions with cardiovascular and behavioral monitoring in marmosets, we show that over-activation of sgACC/25 reduces vagal tone and heart rate variability, alters cortisol dynamics during stress and heightens reactivity to proximal and distal threat. (18)F-FDG PET imaging shows these changes are accompanied by altered activity within a network of brain regions including the amygdala, hypothalamus and dorsolateral prefrontal cortex. Ketamine, shown to have rapid antidepressant effects, fails to reverse elevated arousal to distal threat contrary to the beneficial effects we have previously demonstrated on over-activation induced reward blunting, illustrating the symptom-specificity of its actions. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7588412/ /pubmed/33106488 http://dx.doi.org/10.1038/s41467-020-19167-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Alexander, Laith Wood, Christian M. Gaskin, Philip L. R. Sawiak, Stephen J. Fryer, Tim D. Hong, Young T. McIver, Lauren Clarke, Hannah F. Roberts, Angela C. Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title | Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title_full | Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title_fullStr | Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title_full_unstemmed | Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title_short | Over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
title_sort | over-activation of primate subgenual cingulate cortex enhances the cardiovascular, behavioral and neural responses to threat |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588412/ https://www.ncbi.nlm.nih.gov/pubmed/33106488 http://dx.doi.org/10.1038/s41467-020-19167-0 |
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