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Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding

An animal’s evolutionary success depends on the ability to seek and consume foods while avoiding environmental threats. However, how evolutionarily conserved threat detection circuits modulate feeding is unknown. In mammals, feeding and threat assessment are strongly influenced by the parabrachial n...

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Autores principales: Luskin, Andrew T., Bhatti, Dionnet L., Mulvey, Bernard, Pedersen, Christian E., Girven, Kasey S., Oden-Brunson, Hannah, Kimbell, Kate, Blackburn, Taylor, Sawyer, Abbie, Gereau, Robert W., Dougherty, Joseph D., Bruchas, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909877/
https://www.ncbi.nlm.nih.gov/pubmed/33637526
http://dx.doi.org/10.1126/sciadv.abd3666
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author Luskin, Andrew T.
Bhatti, Dionnet L.
Mulvey, Bernard
Pedersen, Christian E.
Girven, Kasey S.
Oden-Brunson, Hannah
Kimbell, Kate
Blackburn, Taylor
Sawyer, Abbie
Gereau, Robert W.
Dougherty, Joseph D.
Bruchas, Michael R.
author_facet Luskin, Andrew T.
Bhatti, Dionnet L.
Mulvey, Bernard
Pedersen, Christian E.
Girven, Kasey S.
Oden-Brunson, Hannah
Kimbell, Kate
Blackburn, Taylor
Sawyer, Abbie
Gereau, Robert W.
Dougherty, Joseph D.
Bruchas, Michael R.
author_sort Luskin, Andrew T.
collection PubMed
description An animal’s evolutionary success depends on the ability to seek and consume foods while avoiding environmental threats. However, how evolutionarily conserved threat detection circuits modulate feeding is unknown. In mammals, feeding and threat assessment are strongly influenced by the parabrachial nucleus (PBN), a structure that responds to threats and inhibits feeding. Here, we report that the PBN receives dense inputs from two discrete neuronal populations in the bed nucleus of the stria terminalis (BNST), an extended amygdala structure that encodes affective information. Using a series of complementary approaches, we identify opposing BNST-PBN circuits that modulate neuropeptide-expressing PBN neurons to control feeding and affective states. These previously unrecognized neural circuits thus serve as potential nodes of neural circuitry critical for the integration of threat information with the intrinsic drive to feed.
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spelling pubmed-79098772021-03-10 Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding Luskin, Andrew T. Bhatti, Dionnet L. Mulvey, Bernard Pedersen, Christian E. Girven, Kasey S. Oden-Brunson, Hannah Kimbell, Kate Blackburn, Taylor Sawyer, Abbie Gereau, Robert W. Dougherty, Joseph D. Bruchas, Michael R. Sci Adv Research Articles An animal’s evolutionary success depends on the ability to seek and consume foods while avoiding environmental threats. However, how evolutionarily conserved threat detection circuits modulate feeding is unknown. In mammals, feeding and threat assessment are strongly influenced by the parabrachial nucleus (PBN), a structure that responds to threats and inhibits feeding. Here, we report that the PBN receives dense inputs from two discrete neuronal populations in the bed nucleus of the stria terminalis (BNST), an extended amygdala structure that encodes affective information. Using a series of complementary approaches, we identify opposing BNST-PBN circuits that modulate neuropeptide-expressing PBN neurons to control feeding and affective states. These previously unrecognized neural circuits thus serve as potential nodes of neural circuitry critical for the integration of threat information with the intrinsic drive to feed. American Association for the Advancement of Science 2021-02-26 /pmc/articles/PMC7909877/ /pubmed/33637526 http://dx.doi.org/10.1126/sciadv.abd3666 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Luskin, Andrew T.
Bhatti, Dionnet L.
Mulvey, Bernard
Pedersen, Christian E.
Girven, Kasey S.
Oden-Brunson, Hannah
Kimbell, Kate
Blackburn, Taylor
Sawyer, Abbie
Gereau, Robert W.
Dougherty, Joseph D.
Bruchas, Michael R.
Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title_full Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title_fullStr Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title_full_unstemmed Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title_short Extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
title_sort extended amygdala-parabrachial circuits alter threat assessment and regulate feeding
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909877/
https://www.ncbi.nlm.nih.gov/pubmed/33637526
http://dx.doi.org/10.1126/sciadv.abd3666
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