Endogenous opioids regulate moment-to-moment neuronal communication and excitability

The endogenous opioid system regulates fear and anxiety, but the underlying cellular mechanism is unclear. Winterset al. shows that in the intercalated cells (ITC) of the amygdala, endogenous opioids suppress glutamatergic inputs via the δ-opioid receptor presynaptically, and reduce the excitability...

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Autores principales: Bryony L. Winters, Gabrielle C. Gregoriou, Sarah A. Kissiwaa, Oliver A. Wells, Danashi I. Medagoda, Sam M. Hermes, Neil T. Burford, Andrew Alt, Sue A. Aicher, Elena E. Bagley
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Lenguaje:EN
Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/d5dae2c2b5f34eefb24b94cf971ec920
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spelling oai:doaj.org-article:d5dae2c2b5f34eefb24b94cf971ec9202021-12-02T15:38:52ZEndogenous opioids regulate moment-to-moment neuronal communication and excitability10.1038/ncomms146112041-1723https://doaj.org/article/d5dae2c2b5f34eefb24b94cf971ec9202017-03-01T00:00:00Zhttps://doi.org/10.1038/ncomms14611https://doaj.org/toc/2041-1723The endogenous opioid system regulates fear and anxiety, but the underlying cellular mechanism is unclear. Winterset al. shows that in the intercalated cells (ITC) of the amygdala, endogenous opioids suppress glutamatergic inputs via the δ-opioid receptor presynaptically, and reduce the excitability of ITCs via the μ-opioid receptor postsynaptically.Bryony L. WintersGabrielle C. GregoriouSarah A. KissiwaaOliver A. WellsDanashi I. MedagodaSam M. HermesNeil T. BurfordAndrew AltSue A. AicherElena E. BagleyNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Bryony L. Winters
Gabrielle C. Gregoriou
Sarah A. Kissiwaa
Oliver A. Wells
Danashi I. Medagoda
Sam M. Hermes
Neil T. Burford
Andrew Alt
Sue A. Aicher
Elena E. Bagley
Endogenous opioids regulate moment-to-moment neuronal communication and excitability
description The endogenous opioid system regulates fear and anxiety, but the underlying cellular mechanism is unclear. Winterset al. shows that in the intercalated cells (ITC) of the amygdala, endogenous opioids suppress glutamatergic inputs via the δ-opioid receptor presynaptically, and reduce the excitability of ITCs via the μ-opioid receptor postsynaptically.
format article
author Bryony L. Winters
Gabrielle C. Gregoriou
Sarah A. Kissiwaa
Oliver A. Wells
Danashi I. Medagoda
Sam M. Hermes
Neil T. Burford
Andrew Alt
Sue A. Aicher
Elena E. Bagley
author_facet Bryony L. Winters
Gabrielle C. Gregoriou
Sarah A. Kissiwaa
Oliver A. Wells
Danashi I. Medagoda
Sam M. Hermes
Neil T. Burford
Andrew Alt
Sue A. Aicher
Elena E. Bagley
author_sort Bryony L. Winters
title Endogenous opioids regulate moment-to-moment neuronal communication and excitability
title_short Endogenous opioids regulate moment-to-moment neuronal communication and excitability
title_full Endogenous opioids regulate moment-to-moment neuronal communication and excitability
title_fullStr Endogenous opioids regulate moment-to-moment neuronal communication and excitability
title_full_unstemmed Endogenous opioids regulate moment-to-moment neuronal communication and excitability
title_sort endogenous opioids regulate moment-to-moment neuronal communication and excitability
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/d5dae2c2b5f34eefb24b94cf971ec920
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