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Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes

Resveratrol is a phytoalexin found in grapes, red wine, and berries. Resveratrol has been known to have many beneficial health effects, such as anti-cancer, neuroprotective, anti-inflammatory, and life-prolonging effects. However, relatively little is known about the effects of resveratrol on the re...

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Autores principales: Lee, Byung-Hwan, Choi, Sun-Hye, Hwang, Sung-Hee, Kim, Hyeon-Joong, Lee, Joon-Hee, Nah, Seung-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634096/
https://www.ncbi.nlm.nih.gov/pubmed/23626481
http://dx.doi.org/10.4196/kjpp.2013.17.2.175
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author Lee, Byung-Hwan
Choi, Sun-Hye
Hwang, Sung-Hee
Kim, Hyeon-Joong
Lee, Joon-Hee
Nah, Seung-Yeol
author_facet Lee, Byung-Hwan
Choi, Sun-Hye
Hwang, Sung-Hee
Kim, Hyeon-Joong
Lee, Joon-Hee
Nah, Seung-Yeol
author_sort Lee, Byung-Hwan
collection PubMed
description Resveratrol is a phytoalexin found in grapes, red wine, and berries. Resveratrol has been known to have many beneficial health effects, such as anti-cancer, neuroprotective, anti-inflammatory, and life-prolonging effects. However, relatively little is known about the effects of resveratrol on the regulation of ligand-gated ion channels. We have previously reported that resveratrol regulates subsets of homomeric ligand-gated ion channels such as those of 5-HT(3A) receptors. The γ-aminobutyric acid(C) (GABA(C)) receptor is mainly expressed in retinal bipolar cells and plays an important role in visual processing. In the present study, we examined the effects of resveratrol on the channel activity of homomeric GABA(C) receptor expressed in Xenopus oocytes injected with cRNA encoding human GABA(C) ρ subunits. Our data show that the application of GABA elicits an inward peak current (I(GABA)) in oocytes that express the GABA(C) receptor. Resveratrol treatment had no effect on oocytes injected with H(2)O or with GABA(C) receptor cRNA. Co-treatment with resveratrol and GABA inhibited I(GABA) in oocytes with GABA(C) receptors. The inhibition of I(GABA) by resveratrol was in a reversible and concentration-dependent manner. The IC(50) of resveratrol was 28.9±2.8 µM in oocytes expressing GABA(C) receptor. The inhibition of I(GABA) by resveratrol was in voltage-independent and non-competitive manner. These results indicate that resveratrol might regulate GABA(C) receptor expression and that this regulation might be one of the pharmacological actions of resveratrol on the nervous system.
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spelling pubmed-36340962013-04-26 Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes Lee, Byung-Hwan Choi, Sun-Hye Hwang, Sung-Hee Kim, Hyeon-Joong Lee, Joon-Hee Nah, Seung-Yeol Korean J Physiol Pharmacol Original Article Resveratrol is a phytoalexin found in grapes, red wine, and berries. Resveratrol has been known to have many beneficial health effects, such as anti-cancer, neuroprotective, anti-inflammatory, and life-prolonging effects. However, relatively little is known about the effects of resveratrol on the regulation of ligand-gated ion channels. We have previously reported that resveratrol regulates subsets of homomeric ligand-gated ion channels such as those of 5-HT(3A) receptors. The γ-aminobutyric acid(C) (GABA(C)) receptor is mainly expressed in retinal bipolar cells and plays an important role in visual processing. In the present study, we examined the effects of resveratrol on the channel activity of homomeric GABA(C) receptor expressed in Xenopus oocytes injected with cRNA encoding human GABA(C) ρ subunits. Our data show that the application of GABA elicits an inward peak current (I(GABA)) in oocytes that express the GABA(C) receptor. Resveratrol treatment had no effect on oocytes injected with H(2)O or with GABA(C) receptor cRNA. Co-treatment with resveratrol and GABA inhibited I(GABA) in oocytes with GABA(C) receptors. The inhibition of I(GABA) by resveratrol was in a reversible and concentration-dependent manner. The IC(50) of resveratrol was 28.9±2.8 µM in oocytes expressing GABA(C) receptor. The inhibition of I(GABA) by resveratrol was in voltage-independent and non-competitive manner. These results indicate that resveratrol might regulate GABA(C) receptor expression and that this regulation might be one of the pharmacological actions of resveratrol on the nervous system. The Korean Physiological Society and The Korean Society of Pharmacology 2013-04 2013-04-10 /pmc/articles/PMC3634096/ /pubmed/23626481 http://dx.doi.org/10.4196/kjpp.2013.17.2.175 Text en Copyright © 2013 The Korean Physiological Society and The Korean Society of Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Byung-Hwan
Choi, Sun-Hye
Hwang, Sung-Hee
Kim, Hyeon-Joong
Lee, Joon-Hee
Nah, Seung-Yeol
Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title_full Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title_fullStr Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title_full_unstemmed Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title_short Resveratrol Inhibits GABA(C) ρ Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes
title_sort resveratrol inhibits gaba(c) ρ receptor-mediated ion currents expressed in xenopus oocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634096/
https://www.ncbi.nlm.nih.gov/pubmed/23626481
http://dx.doi.org/10.4196/kjpp.2013.17.2.175
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