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Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state
Gonadotropin-releasing hormone (GnRH) neurons form the final pathway for the central neuronal control of fertility. GnRH is released in pulses that vary in frequency in females, helping drive hormonal changes of the reproductive cycle. In the common fertility disorder polycystic ovary syndrome (PCOS...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481724/ https://www.ncbi.nlm.nih.gov/pubmed/32968535 http://dx.doi.org/10.1098/rsos.201040 |
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author | Penix, Jonathon DeFazio, R. Anthony Dulka, Eden A. Schnell, Santiago Moenter, Suzanne M. |
author_facet | Penix, Jonathon DeFazio, R. Anthony Dulka, Eden A. Schnell, Santiago Moenter, Suzanne M. |
author_sort | Penix, Jonathon |
collection | PubMed |
description | Gonadotropin-releasing hormone (GnRH) neurons form the final pathway for the central neuronal control of fertility. GnRH is released in pulses that vary in frequency in females, helping drive hormonal changes of the reproductive cycle. In the common fertility disorder polycystic ovary syndrome (PCOS), persistent high-frequency hormone release is associated with disrupted cycles. We investigated long- and short-term action potential patterns of GnRH neurons in brain slices before and after puberty in female control and prenatally androgenized (PNA) mice, which mimic aspects of PCOS. A Monte Carlo (MC) approach was used to randomize action potential interval order. Dataset distributions were analysed to assess (i) if organization persists in GnRH neuron activity in vitro, and (ii) to determine if any organization changes with development and/or PNA treatment. GnRH neurons in adult control, but not PNA, mice produce long-term patterns different from MC distributions. Short-term patterns differ from MC distributions before puberty but become absorbed into the distributions with maturation, and the distributions narrow. These maturational changes are blunted by PNA treatment. Firing patterns of GnRH neurons in brain slices thus maintain organization dictated at least in part by the biologic status of the source and are disrupted in models of disease. |
format | Online Article Text |
id | pubmed-7481724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74817242020-09-22 Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state Penix, Jonathon DeFazio, R. Anthony Dulka, Eden A. Schnell, Santiago Moenter, Suzanne M. R Soc Open Sci Organismal and Evolutionary Biology Gonadotropin-releasing hormone (GnRH) neurons form the final pathway for the central neuronal control of fertility. GnRH is released in pulses that vary in frequency in females, helping drive hormonal changes of the reproductive cycle. In the common fertility disorder polycystic ovary syndrome (PCOS), persistent high-frequency hormone release is associated with disrupted cycles. We investigated long- and short-term action potential patterns of GnRH neurons in brain slices before and after puberty in female control and prenatally androgenized (PNA) mice, which mimic aspects of PCOS. A Monte Carlo (MC) approach was used to randomize action potential interval order. Dataset distributions were analysed to assess (i) if organization persists in GnRH neuron activity in vitro, and (ii) to determine if any organization changes with development and/or PNA treatment. GnRH neurons in adult control, but not PNA, mice produce long-term patterns different from MC distributions. Short-term patterns differ from MC distributions before puberty but become absorbed into the distributions with maturation, and the distributions narrow. These maturational changes are blunted by PNA treatment. Firing patterns of GnRH neurons in brain slices thus maintain organization dictated at least in part by the biologic status of the source and are disrupted in models of disease. The Royal Society 2020-08-12 /pmc/articles/PMC7481724/ /pubmed/32968535 http://dx.doi.org/10.1098/rsos.201040 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Organismal and Evolutionary Biology Penix, Jonathon DeFazio, R. Anthony Dulka, Eden A. Schnell, Santiago Moenter, Suzanne M. Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title | Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title_full | Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title_fullStr | Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title_full_unstemmed | Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title_short | Firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
title_sort | firing patterns of gonadotropin-releasing hormone neurons are sculpted by their biologic state |
topic | Organismal and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481724/ https://www.ncbi.nlm.nih.gov/pubmed/32968535 http://dx.doi.org/10.1098/rsos.201040 |
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