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Basomedial amygdala mediates top–down control of anxiety and fear
Anxiety-related conditions are among the most difficult neuropsychiatric diseases to treat pharmacologically, but respond to cognitive therapies. There has therefore been interest in identifying relevant top-down pathways from cognitive control regions in medial prefrontal cortex (mPFC). Identificat...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780260/ https://www.ncbi.nlm.nih.gov/pubmed/26536109 http://dx.doi.org/10.1038/nature15698 |
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author | Adhikari, Avishek Lerner, Talia N. Finkelstein, Joel Pak, Sally Jennings, Joshua H. Davidson, Thomas J. Ferenczi, Emily Gunaydin, Lisa A. Mirzabekov, Julie J. Ye, Li Kim, Sung-Yon Lei, Anna Deisseroth, Karl |
author_facet | Adhikari, Avishek Lerner, Talia N. Finkelstein, Joel Pak, Sally Jennings, Joshua H. Davidson, Thomas J. Ferenczi, Emily Gunaydin, Lisa A. Mirzabekov, Julie J. Ye, Li Kim, Sung-Yon Lei, Anna Deisseroth, Karl |
author_sort | Adhikari, Avishek |
collection | PubMed |
description | Anxiety-related conditions are among the most difficult neuropsychiatric diseases to treat pharmacologically, but respond to cognitive therapies. There has therefore been interest in identifying relevant top-down pathways from cognitive control regions in medial prefrontal cortex (mPFC). Identification of such pathways could contribute to our understanding of the cognitive regulation of affect, and provide pathways for intervention. Previous studies have suggested that dorsal and ventral mPFC subregions exert opposing effects on fear, as do subregions of other structures. However, precise causal targets for top-down connections among these diverse possibilities have not been established. Here we show that the basomedial amygdala (BMA) represents the major target of ventral mPFC in amygdala in mice. Moreover, BMA neurons differentiate safe and aversive environments, and BMA activation decreases fear-related freezing and high-anxiety states. Lastly, we show that the ventral mPFC–BMA projection implements top-down control of anxiety state and learned freezing, both at baseline and in stress-induced anxiety, defining a broadly relevant new top-down behavioural regulation pathway. |
format | Online Article Text |
id | pubmed-4780260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-47802602016-05-12 Basomedial amygdala mediates top–down control of anxiety and fear Adhikari, Avishek Lerner, Talia N. Finkelstein, Joel Pak, Sally Jennings, Joshua H. Davidson, Thomas J. Ferenczi, Emily Gunaydin, Lisa A. Mirzabekov, Julie J. Ye, Li Kim, Sung-Yon Lei, Anna Deisseroth, Karl Nature Article Anxiety-related conditions are among the most difficult neuropsychiatric diseases to treat pharmacologically, but respond to cognitive therapies. There has therefore been interest in identifying relevant top-down pathways from cognitive control regions in medial prefrontal cortex (mPFC). Identification of such pathways could contribute to our understanding of the cognitive regulation of affect, and provide pathways for intervention. Previous studies have suggested that dorsal and ventral mPFC subregions exert opposing effects on fear, as do subregions of other structures. However, precise causal targets for top-down connections among these diverse possibilities have not been established. Here we show that the basomedial amygdala (BMA) represents the major target of ventral mPFC in amygdala in mice. Moreover, BMA neurons differentiate safe and aversive environments, and BMA activation decreases fear-related freezing and high-anxiety states. Lastly, we show that the ventral mPFC–BMA projection implements top-down control of anxiety state and learned freezing, both at baseline and in stress-induced anxiety, defining a broadly relevant new top-down behavioural regulation pathway. 2015-11-04 2015-11-12 /pmc/articles/PMC4780260/ /pubmed/26536109 http://dx.doi.org/10.1038/nature15698 Text en http://creativecommons.org/licenses/by/3.0/ Reprints and permissions information is available at www.nature.com/reprints. |
spellingShingle | Article Adhikari, Avishek Lerner, Talia N. Finkelstein, Joel Pak, Sally Jennings, Joshua H. Davidson, Thomas J. Ferenczi, Emily Gunaydin, Lisa A. Mirzabekov, Julie J. Ye, Li Kim, Sung-Yon Lei, Anna Deisseroth, Karl Basomedial amygdala mediates top–down control of anxiety and fear |
title | Basomedial amygdala mediates top–down control of anxiety and fear |
title_full | Basomedial amygdala mediates top–down control of anxiety and fear |
title_fullStr | Basomedial amygdala mediates top–down control of anxiety and fear |
title_full_unstemmed | Basomedial amygdala mediates top–down control of anxiety and fear |
title_short | Basomedial amygdala mediates top–down control of anxiety and fear |
title_sort | basomedial amygdala mediates top–down control of anxiety and fear |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780260/ https://www.ncbi.nlm.nih.gov/pubmed/26536109 http://dx.doi.org/10.1038/nature15698 |
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