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Photosensitive inhibition of the GABA system in vitro

In the central nervous system (CNS), γ–aminobutyric acid A (GABA(A)) receptors mediate two types of inhibitory effects. Phasic inhibition involves the activation of synaptic GABA(A) receptors, and tonic inhibition is mediated by extrasynaptic GABA(A) receptors. GABA(A) receptors are important regula...

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Detalles Bibliográficos
Autores principales: Sun, Lei, Liu, Xinying, Li, Xue, Li, Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035376/
https://www.ncbi.nlm.nih.gov/pubmed/32081949
http://dx.doi.org/10.1038/s41598-020-59915-2
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author Sun, Lei
Liu, Xinying
Li, Xue
Li, Mi
author_facet Sun, Lei
Liu, Xinying
Li, Xue
Li, Mi
author_sort Sun, Lei
collection PubMed
description In the central nervous system (CNS), γ–aminobutyric acid A (GABA(A)) receptors mediate two types of inhibitory effects. Phasic inhibition involves the activation of synaptic GABA(A) receptors, and tonic inhibition is mediated by extrasynaptic GABA(A) receptors. GABA(A) receptors are important regulators of neuronal activity and are involved in a range of neurological disorders. In this study, we conducted sIPSCs recordings on hippocampal CA1 pyramidal neurons in WT SD rats and found that exposure to blue light could specifically block the tonic inhibition and sIPSCs, and regulate neuronal activity. These observations indicate the existence of a non-opsin photosensitive pathway that regulates the GABA inhibitory system in the CNS.
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spelling pubmed-70353762020-02-28 Photosensitive inhibition of the GABA system in vitro Sun, Lei Liu, Xinying Li, Xue Li, Mi Sci Rep Article In the central nervous system (CNS), γ–aminobutyric acid A (GABA(A)) receptors mediate two types of inhibitory effects. Phasic inhibition involves the activation of synaptic GABA(A) receptors, and tonic inhibition is mediated by extrasynaptic GABA(A) receptors. GABA(A) receptors are important regulators of neuronal activity and are involved in a range of neurological disorders. In this study, we conducted sIPSCs recordings on hippocampal CA1 pyramidal neurons in WT SD rats and found that exposure to blue light could specifically block the tonic inhibition and sIPSCs, and regulate neuronal activity. These observations indicate the existence of a non-opsin photosensitive pathway that regulates the GABA inhibitory system in the CNS. Nature Publishing Group UK 2020-02-21 /pmc/articles/PMC7035376/ /pubmed/32081949 http://dx.doi.org/10.1038/s41598-020-59915-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sun, Lei
Liu, Xinying
Li, Xue
Li, Mi
Photosensitive inhibition of the GABA system in vitro
title Photosensitive inhibition of the GABA system in vitro
title_full Photosensitive inhibition of the GABA system in vitro
title_fullStr Photosensitive inhibition of the GABA system in vitro
title_full_unstemmed Photosensitive inhibition of the GABA system in vitro
title_short Photosensitive inhibition of the GABA system in vitro
title_sort photosensitive inhibition of the gaba system in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035376/
https://www.ncbi.nlm.nih.gov/pubmed/32081949
http://dx.doi.org/10.1038/s41598-020-59915-2
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