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Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus
The suprachiasmatic nucleus (SCN), the master circadian clock in mammals, sends major output signals to the subparaventricular zone (SPZ) and further to the paraventricular nucleus (PVN), the neural mechanism of which is largely unknown. In this study, the intracellular calcium levels were measured...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176559/ https://www.ncbi.nlm.nih.gov/pubmed/30228120 http://dx.doi.org/10.1073/pnas.1804300115 |
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author | Wu, Yu-Er Enoki, Ryosuke Oda, Yoshiaki Huang, Zhi-Li Honma, Ken-ichi Honma, Sato |
author_facet | Wu, Yu-Er Enoki, Ryosuke Oda, Yoshiaki Huang, Zhi-Li Honma, Ken-ichi Honma, Sato |
author_sort | Wu, Yu-Er |
collection | PubMed |
description | The suprachiasmatic nucleus (SCN), the master circadian clock in mammals, sends major output signals to the subparaventricular zone (SPZ) and further to the paraventricular nucleus (PVN), the neural mechanism of which is largely unknown. In this study, the intracellular calcium levels were measured continuously in cultured hypothalamic slices containing the PVN, SPZ, and SCN. We detected ultradian calcium rhythms in both the SPZ-PVN and SCN regions with periods of 0.5–4.0 hours, the frequency of which depended on the local circadian rhythm in the SPZ-PVN region. The ultradian rhythms were synchronous in the entire SPZ-PVN region and a part of the SCN. Because the ultradian rhythms were not detected in the SCN-only slice, the origin of ultradian rhythm is the SPZ-PVN region. In association with an ultradian bout, a rapid increase of intracellular calcium in a millisecond order was detected, the frequency of which determined the amplitude of an ultradian bout. The synchronous ultradian rhythms were desynchronized and depressed by a sodium channel blocker tetrodotoxin, suggesting that a tetrodotoxin-sensitive network is involved in synchrony of the ultradian bouts. In contrast, the ultradian rhythm is abolished by glutamate receptor blockers, indicating the critical role of glutamatergic mechanism in ultradian rhythm generation, while a GABA(A) receptor blocker increased the frequency of ultradian rhythm and modified the circadian rhythm in the SCN. A GABAergic network may refine the circadian output signals. The present study provides a clue to unraveling the loci and network mechanisms of the ultradian rhythm. |
format | Online Article Text |
id | pubmed-6176559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-61765592018-10-11 Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus Wu, Yu-Er Enoki, Ryosuke Oda, Yoshiaki Huang, Zhi-Li Honma, Ken-ichi Honma, Sato Proc Natl Acad Sci U S A PNAS Plus The suprachiasmatic nucleus (SCN), the master circadian clock in mammals, sends major output signals to the subparaventricular zone (SPZ) and further to the paraventricular nucleus (PVN), the neural mechanism of which is largely unknown. In this study, the intracellular calcium levels were measured continuously in cultured hypothalamic slices containing the PVN, SPZ, and SCN. We detected ultradian calcium rhythms in both the SPZ-PVN and SCN regions with periods of 0.5–4.0 hours, the frequency of which depended on the local circadian rhythm in the SPZ-PVN region. The ultradian rhythms were synchronous in the entire SPZ-PVN region and a part of the SCN. Because the ultradian rhythms were not detected in the SCN-only slice, the origin of ultradian rhythm is the SPZ-PVN region. In association with an ultradian bout, a rapid increase of intracellular calcium in a millisecond order was detected, the frequency of which determined the amplitude of an ultradian bout. The synchronous ultradian rhythms were desynchronized and depressed by a sodium channel blocker tetrodotoxin, suggesting that a tetrodotoxin-sensitive network is involved in synchrony of the ultradian bouts. In contrast, the ultradian rhythm is abolished by glutamate receptor blockers, indicating the critical role of glutamatergic mechanism in ultradian rhythm generation, while a GABA(A) receptor blocker increased the frequency of ultradian rhythm and modified the circadian rhythm in the SCN. A GABAergic network may refine the circadian output signals. The present study provides a clue to unraveling the loci and network mechanisms of the ultradian rhythm. National Academy of Sciences 2018-10-02 2018-09-18 /pmc/articles/PMC6176559/ /pubmed/30228120 http://dx.doi.org/10.1073/pnas.1804300115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | PNAS Plus Wu, Yu-Er Enoki, Ryosuke Oda, Yoshiaki Huang, Zhi-Li Honma, Ken-ichi Honma, Sato Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title | Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title_full | Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title_fullStr | Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title_full_unstemmed | Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title_short | Ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
title_sort | ultradian calcium rhythms in the paraventricular nucleus and subparaventricular zone in the hypothalamus |
topic | PNAS Plus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176559/ https://www.ncbi.nlm.nih.gov/pubmed/30228120 http://dx.doi.org/10.1073/pnas.1804300115 |
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