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Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice
The mechanism by which arcuate kisspeptin (ARN(KISS)) neurons co-expressing glutamate, neurokinin B, and dynorphin intermittently synchronize their activity to drive pulsatile hormone secretion remains unclear in females. In order to study spontaneous synchronization within the ARN(KISS) neuron netw...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652333/ https://www.ncbi.nlm.nih.gov/pubmed/37936337 http://dx.doi.org/10.1210/endocr/bqad167 |
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author | Morris, Paul G Herbison, Allan E |
author_facet | Morris, Paul G Herbison, Allan E |
author_sort | Morris, Paul G |
collection | PubMed |
description | The mechanism by which arcuate kisspeptin (ARN(KISS)) neurons co-expressing glutamate, neurokinin B, and dynorphin intermittently synchronize their activity to drive pulsatile hormone secretion remains unclear in females. In order to study spontaneous synchronization within the ARN(KISS) neuron network, acute brain slices were prepared from adult female Kiss1-GCaMP6 mice. Analysis of both spontaneous synchronizations and those driven by high frequency stimulation of individual ARN(KISS) neurons revealed that the network exhibits semi-random emergent excitation dependent upon glutamate signaling through AMPA receptors. No role for NMDA receptors was identified. In contrast to male mice, ongoing tachykinin receptor tone within the slice operated to promote spontaneous synchronizations in females. As previously observed in males, we found that ongoing dynorphin transmission in the slice did not contribute to synchronization events. These observations indicate that a very similar AMPA receptor–dependent mechanism underlies ARN(KISS) neuron synchronizations in the female mouse supporting the “glutamate two-transition” model for kisspeptin neuron synchronization. However, a potentially important sex difference appears to exist with a more prominent facilitatory role for tachykinin transmission in the female. |
format | Online Article Text |
id | pubmed-10652333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106523332023-11-04 Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice Morris, Paul G Herbison, Allan E Endocrinology Research Article The mechanism by which arcuate kisspeptin (ARN(KISS)) neurons co-expressing glutamate, neurokinin B, and dynorphin intermittently synchronize their activity to drive pulsatile hormone secretion remains unclear in females. In order to study spontaneous synchronization within the ARN(KISS) neuron network, acute brain slices were prepared from adult female Kiss1-GCaMP6 mice. Analysis of both spontaneous synchronizations and those driven by high frequency stimulation of individual ARN(KISS) neurons revealed that the network exhibits semi-random emergent excitation dependent upon glutamate signaling through AMPA receptors. No role for NMDA receptors was identified. In contrast to male mice, ongoing tachykinin receptor tone within the slice operated to promote spontaneous synchronizations in females. As previously observed in males, we found that ongoing dynorphin transmission in the slice did not contribute to synchronization events. These observations indicate that a very similar AMPA receptor–dependent mechanism underlies ARN(KISS) neuron synchronizations in the female mouse supporting the “glutamate two-transition” model for kisspeptin neuron synchronization. However, a potentially important sex difference appears to exist with a more prominent facilitatory role for tachykinin transmission in the female. Oxford University Press 2023-11-04 /pmc/articles/PMC10652333/ /pubmed/37936337 http://dx.doi.org/10.1210/endocr/bqad167 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Morris, Paul G Herbison, Allan E Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title | Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title_full | Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title_fullStr | Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title_full_unstemmed | Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title_short | Mechanism of Arcuate Kisspeptin Neuron Synchronization in Acute Brain Slices From Female Mice |
title_sort | mechanism of arcuate kisspeptin neuron synchronization in acute brain slices from female mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652333/ https://www.ncbi.nlm.nih.gov/pubmed/37936337 http://dx.doi.org/10.1210/endocr/bqad167 |
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