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The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats

Variations in circulating corticosterone (Cort) are driven by the paraventricular nucleus of the hypothalamus (PVN), mainly via the sympathetic autonomic nervous system (ANS) directly stimulating Cort release from the adrenal gland and via corticotropin-releasing hormone targeting the adenohypophysi...

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Autores principales: Leon-Mercado, Luis, Herrera Moro Chao, Daniela, Basualdo, María del Carmen, Kawata, Mitsuhiro, Escobar, Carolina, Buijs, Ruud M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334455/
https://www.ncbi.nlm.nih.gov/pubmed/28275717
http://dx.doi.org/10.1523/ENEURO.0350-16.2017
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author Leon-Mercado, Luis
Herrera Moro Chao, Daniela
Basualdo, María del Carmen
Kawata, Mitsuhiro
Escobar, Carolina
Buijs, Ruud M.
author_facet Leon-Mercado, Luis
Herrera Moro Chao, Daniela
Basualdo, María del Carmen
Kawata, Mitsuhiro
Escobar, Carolina
Buijs, Ruud M.
author_sort Leon-Mercado, Luis
collection PubMed
description Variations in circulating corticosterone (Cort) are driven by the paraventricular nucleus of the hypothalamus (PVN), mainly via the sympathetic autonomic nervous system (ANS) directly stimulating Cort release from the adrenal gland and via corticotropin-releasing hormone targeting the adenohypophysis to release adrenocorticotropic hormone (ACTH). Cort feeds back through glucocorticoid receptors (GRs). Here we show in male Wistar rats that PVN neurons projecting to the adrenal gland do not express GRs, leaving the question of how the ANS in the PVN gets information about circulating Cort levels to control the adrenal. Since the arcuate nucleus (ARC) shows a less restrictive blood–brain barrier, expresses GRs, and projects to the PVN, we investigated whether the ARC can detect and produce fast adjustments of circulating Cort. In low Cort conditions (morning), local microdialysis in the ARC with type I GR antagonist produced a fast and sustained increase of Cort. This was not observed with a type II antagonist. At the circadian peak levels of Cort (afternoon), a type II GR antagonist, but not a type I antagonist, increased Cort levels but not ACTH levels. Antagonist infusions in the PVN did not modify circulating Cort levels, demonstrating the specificity of the ARC to give Cort negative feedback. Furthermore, type I and II GR agonists in the ARC prevented the increase of Cort after stress, demonstrating the role of the ARC as sensor to modulate Cort release. Our findings show that the ARC may be essential to sense blood levels of Cort and adapt Cort secretion depending on such conditions as stress or time of day.
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spelling pubmed-53344552017-03-08 The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats Leon-Mercado, Luis Herrera Moro Chao, Daniela Basualdo, María del Carmen Kawata, Mitsuhiro Escobar, Carolina Buijs, Ruud M. eNeuro New Research Variations in circulating corticosterone (Cort) are driven by the paraventricular nucleus of the hypothalamus (PVN), mainly via the sympathetic autonomic nervous system (ANS) directly stimulating Cort release from the adrenal gland and via corticotropin-releasing hormone targeting the adenohypophysis to release adrenocorticotropic hormone (ACTH). Cort feeds back through glucocorticoid receptors (GRs). Here we show in male Wistar rats that PVN neurons projecting to the adrenal gland do not express GRs, leaving the question of how the ANS in the PVN gets information about circulating Cort levels to control the adrenal. Since the arcuate nucleus (ARC) shows a less restrictive blood–brain barrier, expresses GRs, and projects to the PVN, we investigated whether the ARC can detect and produce fast adjustments of circulating Cort. In low Cort conditions (morning), local microdialysis in the ARC with type I GR antagonist produced a fast and sustained increase of Cort. This was not observed with a type II antagonist. At the circadian peak levels of Cort (afternoon), a type II GR antagonist, but not a type I antagonist, increased Cort levels but not ACTH levels. Antagonist infusions in the PVN did not modify circulating Cort levels, demonstrating the specificity of the ARC to give Cort negative feedback. Furthermore, type I and II GR agonists in the ARC prevented the increase of Cort after stress, demonstrating the role of the ARC as sensor to modulate Cort release. Our findings show that the ARC may be essential to sense blood levels of Cort and adapt Cort secretion depending on such conditions as stress or time of day. Society for Neuroscience 2017-03-02 /pmc/articles/PMC5334455/ /pubmed/28275717 http://dx.doi.org/10.1523/ENEURO.0350-16.2017 Text en Copyright © 2017 Leon-Mercado et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Leon-Mercado, Luis
Herrera Moro Chao, Daniela
Basualdo, María del Carmen
Kawata, Mitsuhiro
Escobar, Carolina
Buijs, Ruud M.
The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title_full The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title_fullStr The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title_full_unstemmed The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title_short The Arcuate Nucleus: A Site of Fast Negative Feedback for Corticosterone Secretion in Male Rats
title_sort arcuate nucleus: a site of fast negative feedback for corticosterone secretion in male rats
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334455/
https://www.ncbi.nlm.nih.gov/pubmed/28275717
http://dx.doi.org/10.1523/ENEURO.0350-16.2017
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