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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...

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Autores principales: Penix, Jonathon, DeFazio, R. Anthony, Dulka, Eden A., Schnell, Santiago, Moenter, Suzanne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
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.
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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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