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A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats

Survival depends on a balance between seeking rewards and avoiding potential threats, but the neural circuits that regulate this motivational conflict remain largely unknown. Using an approach-food vs. avoid-predator threat conflict test in rats, we identified a subpopulation of neurons in the anter...

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Autores principales: Engelke, D. S., Zhang, X. O., O’Malley, J. J., Fernandez-Leon, J. A., Li, S., Kirouac, G. J., Beierlein, M., Do-Monte, F. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097010/
https://www.ncbi.nlm.nih.gov/pubmed/33947849
http://dx.doi.org/10.1038/s41467-021-22730-y
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author Engelke, D. S.
Zhang, X. O.
O’Malley, J. J.
Fernandez-Leon, J. A.
Li, S.
Kirouac, G. J.
Beierlein, M.
Do-Monte, F. H.
author_facet Engelke, D. S.
Zhang, X. O.
O’Malley, J. J.
Fernandez-Leon, J. A.
Li, S.
Kirouac, G. J.
Beierlein, M.
Do-Monte, F. H.
author_sort Engelke, D. S.
collection PubMed
description Survival depends on a balance between seeking rewards and avoiding potential threats, but the neural circuits that regulate this motivational conflict remain largely unknown. Using an approach-food vs. avoid-predator threat conflict test in rats, we identified a subpopulation of neurons in the anterior portion of the paraventricular thalamic nucleus (aPVT) which express corticotrophin-releasing factor (CRF) and are preferentially recruited during conflict. Inactivation of aPVT(CRF) neurons during conflict biases animal’s response toward food, whereas activation of these cells recapitulates the food-seeking suppression observed during conflict. aPVT(CRF) neurons project densely to the nucleus accumbens (NAc), and activity in this pathway reduces food seeking and increases avoidance. In addition, we identified the ventromedial hypothalamus (VMH) as a critical input to aPVT(CRF) neurons, and demonstrated that VMH-aPVT neurons mediate defensive behaviors exclusively during conflict. Together, our findings describe a hypothalamic-thalamostriatal circuit that suppresses reward-seeking behavior under the competing demands of avoiding threats.
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spelling pubmed-80970102021-05-11 A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats Engelke, D. S. Zhang, X. O. O’Malley, J. J. Fernandez-Leon, J. A. Li, S. Kirouac, G. J. Beierlein, M. Do-Monte, F. H. Nat Commun Article Survival depends on a balance between seeking rewards and avoiding potential threats, but the neural circuits that regulate this motivational conflict remain largely unknown. Using an approach-food vs. avoid-predator threat conflict test in rats, we identified a subpopulation of neurons in the anterior portion of the paraventricular thalamic nucleus (aPVT) which express corticotrophin-releasing factor (CRF) and are preferentially recruited during conflict. Inactivation of aPVT(CRF) neurons during conflict biases animal’s response toward food, whereas activation of these cells recapitulates the food-seeking suppression observed during conflict. aPVT(CRF) neurons project densely to the nucleus accumbens (NAc), and activity in this pathway reduces food seeking and increases avoidance. In addition, we identified the ventromedial hypothalamus (VMH) as a critical input to aPVT(CRF) neurons, and demonstrated that VMH-aPVT neurons mediate defensive behaviors exclusively during conflict. Together, our findings describe a hypothalamic-thalamostriatal circuit that suppresses reward-seeking behavior under the competing demands of avoiding threats. Nature Publishing Group UK 2021-05-04 /pmc/articles/PMC8097010/ /pubmed/33947849 http://dx.doi.org/10.1038/s41467-021-22730-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Engelke, D. S.
Zhang, X. O.
O’Malley, J. J.
Fernandez-Leon, J. A.
Li, S.
Kirouac, G. J.
Beierlein, M.
Do-Monte, F. H.
A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title_full A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title_fullStr A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title_full_unstemmed A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title_short A hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
title_sort hypothalamic-thalamostriatal circuit that controls approach-avoidance conflict in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097010/
https://www.ncbi.nlm.nih.gov/pubmed/33947849
http://dx.doi.org/10.1038/s41467-021-22730-y
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