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Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum
In vertebrates, gonadotropin-releasing hormone (GnRH)-secreting neurons control fertility by regulating gonadotrophs in the anterior pituitary. While it is known that acetylcholine (ACh) influences GnRH secretion, whether the effect is direct or indirect, and the specific ACh receptor (AChR) subtype...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025473/ https://www.ncbi.nlm.nih.gov/pubmed/36950690 http://dx.doi.org/10.3389/fendo.2023.1147554 |
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author | Shostak, David M. Constantin, Stephanie Flannery, Jill Wray, Susan |
author_facet | Shostak, David M. Constantin, Stephanie Flannery, Jill Wray, Susan |
author_sort | Shostak, David M. |
collection | PubMed |
description | In vertebrates, gonadotropin-releasing hormone (GnRH)-secreting neurons control fertility by regulating gonadotrophs in the anterior pituitary. While it is known that acetylcholine (ACh) influences GnRH secretion, whether the effect is direct or indirect, and the specific ACh receptor (AChR) subtype(s) involved remain unclear. Here, we determined 1) whether ACh can modulate GnRH cellular activity and 2) a source of ACh afferents contacting GnRH neurons. Calcium imaging was used to assay GnRH neuronal activity. With GABAergic and glutamatergic transmission blocked, subtype-specific AChR agonists and antagonists were applied to identify direct regulation of GnRH neurons. ACh and nicotine caused a rise in calcium that declined gradually back to baseline after 5-6 min. This response was mimicked by an alpha3-specific agonist. In contrast, muscarine inhibited GnRH calcium oscillations, and blocking M2 and M4 together prevented this inhibition. Labeling for choline acetyltransferase (ChAT) and GnRH revealed ChAT fibers contacting GnRH neurons, primarily in the medial septum (MS), and in greater number in females than males. ChAT positive cells in the MS are known to express p75NGFRs. Labeling for p75NGFR, ChAT and GnRH indicated that ChAT fibers contacting GnRH cells originate from cholinergic cells within these same rostral areas. Together, these results indicate that cholinergic cells in septal areas can directly regulate GnRH neurons. |
format | Online Article Text |
id | pubmed-10025473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100254732023-03-21 Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum Shostak, David M. Constantin, Stephanie Flannery, Jill Wray, Susan Front Endocrinol (Lausanne) Endocrinology In vertebrates, gonadotropin-releasing hormone (GnRH)-secreting neurons control fertility by regulating gonadotrophs in the anterior pituitary. While it is known that acetylcholine (ACh) influences GnRH secretion, whether the effect is direct or indirect, and the specific ACh receptor (AChR) subtype(s) involved remain unclear. Here, we determined 1) whether ACh can modulate GnRH cellular activity and 2) a source of ACh afferents contacting GnRH neurons. Calcium imaging was used to assay GnRH neuronal activity. With GABAergic and glutamatergic transmission blocked, subtype-specific AChR agonists and antagonists were applied to identify direct regulation of GnRH neurons. ACh and nicotine caused a rise in calcium that declined gradually back to baseline after 5-6 min. This response was mimicked by an alpha3-specific agonist. In contrast, muscarine inhibited GnRH calcium oscillations, and blocking M2 and M4 together prevented this inhibition. Labeling for choline acetyltransferase (ChAT) and GnRH revealed ChAT fibers contacting GnRH neurons, primarily in the medial septum (MS), and in greater number in females than males. ChAT positive cells in the MS are known to express p75NGFRs. Labeling for p75NGFR, ChAT and GnRH indicated that ChAT fibers contacting GnRH cells originate from cholinergic cells within these same rostral areas. Together, these results indicate that cholinergic cells in septal areas can directly regulate GnRH neurons. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10025473/ /pubmed/36950690 http://dx.doi.org/10.3389/fendo.2023.1147554 Text en Copyright © 2023 Shostak, Constantin, Flannery and Wray https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Shostak, David M. Constantin, Stephanie Flannery, Jill Wray, Susan Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title | Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title_full | Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title_fullStr | Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title_full_unstemmed | Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title_short | Acetylcholine regulation of GnRH neuronal activity: A circuit in the medial septum |
title_sort | acetylcholine regulation of gnrh neuronal activity: a circuit in the medial septum |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025473/ https://www.ncbi.nlm.nih.gov/pubmed/36950690 http://dx.doi.org/10.3389/fendo.2023.1147554 |
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