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Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior
An adaptive stress response involves various mediators and circuits orchestrating a complex interplay of physiological, emotional, and behavioral adjustments. We identified a population of corticotropin-releasing hormone (CRH) neurons in the lateral part of the interstitial nucleus of the anterior c...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668302/ https://www.ncbi.nlm.nih.gov/pubmed/36383658 http://dx.doi.org/10.1126/sciadv.abo1023 |
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author | Chang, Simon Fermani, Federica Lao, Chu-Lan Huang, Lianyun Jakovcevski, Mira Di Giaimo, Rossella Gagliardi, Miriam Menegaz, Danusa Hennrich, Alexandru Adrian Ziller, Michael Eder, Matthias Klein, Rüdiger Cai, Na Deussing, Jan M. |
author_facet | Chang, Simon Fermani, Federica Lao, Chu-Lan Huang, Lianyun Jakovcevski, Mira Di Giaimo, Rossella Gagliardi, Miriam Menegaz, Danusa Hennrich, Alexandru Adrian Ziller, Michael Eder, Matthias Klein, Rüdiger Cai, Na Deussing, Jan M. |
author_sort | Chang, Simon |
collection | PubMed |
description | An adaptive stress response involves various mediators and circuits orchestrating a complex interplay of physiological, emotional, and behavioral adjustments. We identified a population of corticotropin-releasing hormone (CRH) neurons in the lateral part of the interstitial nucleus of the anterior commissure (IPACL), a subdivision of the extended amygdala, which exclusively innervate the substantia nigra (SN). Specific stimulation of this circuit elicits hyperactivation of the hypothalamic-pituitary-adrenal axis, locomotor activation, and avoidance behavior contingent on CRH receptor type 1 (CRHR1) located at axon terminals in the SN, which originate from external globus pallidus (GPe) neurons. The neuronal activity prompting the observed behavior is shaped by IPACL(CRH) and GPe(CRHR1) neurons coalescing in the SN. These results delineate a previously unidentified tripartite CRH circuit functionally connecting extended amygdala and basal ganglia nuclei to drive locomotor activation and avoidance behavior. |
format | Online Article Text |
id | pubmed-9668302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96683022022-11-29 Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior Chang, Simon Fermani, Federica Lao, Chu-Lan Huang, Lianyun Jakovcevski, Mira Di Giaimo, Rossella Gagliardi, Miriam Menegaz, Danusa Hennrich, Alexandru Adrian Ziller, Michael Eder, Matthias Klein, Rüdiger Cai, Na Deussing, Jan M. Sci Adv Neuroscience An adaptive stress response involves various mediators and circuits orchestrating a complex interplay of physiological, emotional, and behavioral adjustments. We identified a population of corticotropin-releasing hormone (CRH) neurons in the lateral part of the interstitial nucleus of the anterior commissure (IPACL), a subdivision of the extended amygdala, which exclusively innervate the substantia nigra (SN). Specific stimulation of this circuit elicits hyperactivation of the hypothalamic-pituitary-adrenal axis, locomotor activation, and avoidance behavior contingent on CRH receptor type 1 (CRHR1) located at axon terminals in the SN, which originate from external globus pallidus (GPe) neurons. The neuronal activity prompting the observed behavior is shaped by IPACL(CRH) and GPe(CRHR1) neurons coalescing in the SN. These results delineate a previously unidentified tripartite CRH circuit functionally connecting extended amygdala and basal ganglia nuclei to drive locomotor activation and avoidance behavior. American Association for the Advancement of Science 2022-11-16 /pmc/articles/PMC9668302/ /pubmed/36383658 http://dx.doi.org/10.1126/sciadv.abo1023 Text en Copyright © 2022 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/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 | Neuroscience Chang, Simon Fermani, Federica Lao, Chu-Lan Huang, Lianyun Jakovcevski, Mira Di Giaimo, Rossella Gagliardi, Miriam Menegaz, Danusa Hennrich, Alexandru Adrian Ziller, Michael Eder, Matthias Klein, Rüdiger Cai, Na Deussing, Jan M. Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title | Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title_full | Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title_fullStr | Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title_full_unstemmed | Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title_short | Tripartite extended amygdala–basal ganglia CRH circuit drives locomotor activation and avoidance behavior |
title_sort | tripartite extended amygdala–basal ganglia crh circuit drives locomotor activation and avoidance behavior |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668302/ https://www.ncbi.nlm.nih.gov/pubmed/36383658 http://dx.doi.org/10.1126/sciadv.abo1023 |
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