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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...

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Autores principales: Qiu, Jian, Nestor, Casey C, Zhang, Chunguang, Padilla, Stephanie L, Palmiter, Richard D, Kelly, Martin J, Rønnekleiv, Oline K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
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
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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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