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High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons
Kisspeptin (Kiss1) and neurokinin B (NKB) neurocircuits are essential for pubertal development and fertility. Kisspeptin neurons in the hypothalamic arcuate nucleus (Kiss1(ARH)) co-express Kiss1, NKB, dynorphin and glutamate and are postulated to provide an episodic, excitatory drive to gonadotropin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995096/ https://www.ncbi.nlm.nih.gov/pubmed/27549338 http://dx.doi.org/10.7554/eLife.16246 |
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author | Qiu, Jian Nestor, Casey C Zhang, Chunguang Padilla, Stephanie L Palmiter, Richard D Kelly, Martin J Rønnekleiv, Oline K |
author_facet | Qiu, Jian Nestor, Casey C Zhang, Chunguang Padilla, Stephanie L Palmiter, Richard D Kelly, Martin J Rønnekleiv, Oline K |
author_sort | Qiu, Jian |
collection | PubMed |
description | Kisspeptin (Kiss1) and neurokinin B (NKB) neurocircuits are essential for pubertal development and fertility. Kisspeptin neurons in the hypothalamic arcuate nucleus (Kiss1(ARH)) co-express Kiss1, NKB, dynorphin and glutamate and are postulated to provide an episodic, excitatory drive to gonadotropin-releasing hormone 1 (GnRH) neurons, the synaptic mechanisms of which are unknown. We characterized the cellular basis for synchronized Kiss1(ARH) neuronal activity using optogenetics, whole-cell electrophysiology, molecular pharmacology and single cell RT-PCR in mice. High-frequency photostimulation of Kiss1(ARH) neurons evoked local release of excitatory (NKB) and inhibitory (dynorphin) neuropeptides, which were found to synchronize the Kiss1(ARH) neuronal firing. The light-evoked synchronous activity caused robust excitation of GnRH neurons by a synaptic mechanism that also involved glutamatergic input to preoptic Kiss1 neurons from Kiss1(ARH) neurons. We propose that Kiss1(ARH) neurons play a dual role of driving episodic secretion of GnRH through the differential release of peptide and amino acid neurotransmitters to coordinate reproductive function. DOI: http://dx.doi.org/10.7554/eLife.16246.001 |
format | Online Article Text |
id | pubmed-4995096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49950962016-08-24 High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons Qiu, Jian Nestor, Casey C Zhang, Chunguang Padilla, Stephanie L Palmiter, Richard D Kelly, Martin J Rønnekleiv, Oline K eLife Neuroscience Kisspeptin (Kiss1) and neurokinin B (NKB) neurocircuits are essential for pubertal development and fertility. Kisspeptin neurons in the hypothalamic arcuate nucleus (Kiss1(ARH)) co-express Kiss1, NKB, dynorphin and glutamate and are postulated to provide an episodic, excitatory drive to gonadotropin-releasing hormone 1 (GnRH) neurons, the synaptic mechanisms of which are unknown. We characterized the cellular basis for synchronized Kiss1(ARH) neuronal activity using optogenetics, whole-cell electrophysiology, molecular pharmacology and single cell RT-PCR in mice. High-frequency photostimulation of Kiss1(ARH) neurons evoked local release of excitatory (NKB) and inhibitory (dynorphin) neuropeptides, which were found to synchronize the Kiss1(ARH) neuronal firing. The light-evoked synchronous activity caused robust excitation of GnRH neurons by a synaptic mechanism that also involved glutamatergic input to preoptic Kiss1 neurons from Kiss1(ARH) neurons. We propose that Kiss1(ARH) neurons play a dual role of driving episodic secretion of GnRH through the differential release of peptide and amino acid neurotransmitters to coordinate reproductive function. DOI: http://dx.doi.org/10.7554/eLife.16246.001 eLife Sciences Publications, Ltd 2016-08-23 /pmc/articles/PMC4995096/ /pubmed/27549338 http://dx.doi.org/10.7554/eLife.16246 Text en © 2016, Qiu et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Qiu, Jian Nestor, Casey C Zhang, Chunguang Padilla, Stephanie L Palmiter, Richard D Kelly, Martin J Rønnekleiv, Oline K High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title | High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title_full | High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title_fullStr | High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title_full_unstemmed | High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title_short | High-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites GnRH neurons |
title_sort | high-frequency stimulation-induced peptide release synchronizes arcuate kisspeptin neurons and excites gnrh neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995096/ https://www.ncbi.nlm.nih.gov/pubmed/27549338 http://dx.doi.org/10.7554/eLife.16246 |
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