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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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