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Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice
BACKGROUND: The neuroendocrine control of ovulation is orchestrated by neuronal circuits that ultimately drive the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus to trigger the preovulatory surge in luteinizing hormone (LH) secretion. While estrogen feedback signals are deter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602649/ https://www.ncbi.nlm.nih.gov/pubmed/37900129 http://dx.doi.org/10.3389/fendo.2023.1212854 |
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author | Buo, Carrie Bearss, Robin J. Novak, Alyssa G. Anello, Anna E. Dakin, Jordan J. Piet, Richard |
author_facet | Buo, Carrie Bearss, Robin J. Novak, Alyssa G. Anello, Anna E. Dakin, Jordan J. Piet, Richard |
author_sort | Buo, Carrie |
collection | PubMed |
description | BACKGROUND: The neuroendocrine control of ovulation is orchestrated by neuronal circuits that ultimately drive the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus to trigger the preovulatory surge in luteinizing hormone (LH) secretion. While estrogen feedback signals are determinant in triggering activation of GnRH neurons, through stimulation of afferent kisspeptin neurons in the rostral periventricular area of the third ventricle (RP3V(KISS1) neurons), many neuropeptidergic and classical neurotransmitter systems have been shown to regulate the LH surge. Among these, several lines of evidence indicate that the monoamine neurotransmitter serotonin (5-HT) has an excitatory, permissive, influence over the generation of the surge, via activation of type 2 5-HT (5-HT(2)) receptors. The mechanisms through which this occurs, however, are not well understood. We hypothesized that 5-HT exerts its influence on the surge by stimulating RP3V(KISS1) neurons in a 5-HT(2) receptor-dependent manner. METHODS: We tested this using kisspeptin neuron-specific calcium imaging and electrophysiology in brain slices obtained from male and female mice. RESULTS: We show that exogenous 5-HT reversibly increases the activity of the majority of RP3V(KISS1) neurons. This effect is more prominent in females than in males, is likely mediated directly at RP3V(KISS1) neurons and requires activation of 5-HT(2) receptors. The functional impact of 5-HT on RP3V(KISS1) neurons, however, does not significantly vary during the estrous cycle. CONCLUSION: Taken together, these data suggest that 5-HT(2) receptor-mediated stimulation of RP3V(KISS1) neuron activity might be involved in mediating the influence of 5-HT on the preovulatory LH surge. |
format | Online Article Text |
id | pubmed-10602649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106026492023-10-27 Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice Buo, Carrie Bearss, Robin J. Novak, Alyssa G. Anello, Anna E. Dakin, Jordan J. Piet, Richard Front Endocrinol (Lausanne) Endocrinology BACKGROUND: The neuroendocrine control of ovulation is orchestrated by neuronal circuits that ultimately drive the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus to trigger the preovulatory surge in luteinizing hormone (LH) secretion. While estrogen feedback signals are determinant in triggering activation of GnRH neurons, through stimulation of afferent kisspeptin neurons in the rostral periventricular area of the third ventricle (RP3V(KISS1) neurons), many neuropeptidergic and classical neurotransmitter systems have been shown to regulate the LH surge. Among these, several lines of evidence indicate that the monoamine neurotransmitter serotonin (5-HT) has an excitatory, permissive, influence over the generation of the surge, via activation of type 2 5-HT (5-HT(2)) receptors. The mechanisms through which this occurs, however, are not well understood. We hypothesized that 5-HT exerts its influence on the surge by stimulating RP3V(KISS1) neurons in a 5-HT(2) receptor-dependent manner. METHODS: We tested this using kisspeptin neuron-specific calcium imaging and electrophysiology in brain slices obtained from male and female mice. RESULTS: We show that exogenous 5-HT reversibly increases the activity of the majority of RP3V(KISS1) neurons. This effect is more prominent in females than in males, is likely mediated directly at RP3V(KISS1) neurons and requires activation of 5-HT(2) receptors. The functional impact of 5-HT on RP3V(KISS1) neurons, however, does not significantly vary during the estrous cycle. CONCLUSION: Taken together, these data suggest that 5-HT(2) receptor-mediated stimulation of RP3V(KISS1) neuron activity might be involved in mediating the influence of 5-HT on the preovulatory LH surge. Frontiers Media S.A. 2023-10-12 /pmc/articles/PMC10602649/ /pubmed/37900129 http://dx.doi.org/10.3389/fendo.2023.1212854 Text en Copyright © 2023 Buo, Bearss, Novak, Anello, Dakin and Piet 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 Buo, Carrie Bearss, Robin J. Novak, Alyssa G. Anello, Anna E. Dakin, Jordan J. Piet, Richard Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title | Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title_full | Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title_fullStr | Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title_full_unstemmed | Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title_short | Serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
title_sort | serotonin stimulates female preoptic area kisspeptin neurons via activation of type 2 serotonin receptors in mice |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602649/ https://www.ncbi.nlm.nih.gov/pubmed/37900129 http://dx.doi.org/10.3389/fendo.2023.1212854 |
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