Resveratrol Inhibits GABAC rho Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes.
10.4196/kjpp.2013.17.2.175
- Author:
Byung Hwan LEE
1
;
Sun Hye CHOI
;
Sung Hee HWANG
;
Hyeon Joong KIM
;
Joon Hee LEE
;
Seung Yeol NAH
Author Information
1. Department of Physiology, College of Veterinary Medicine and Bio-Molecular Informatics Center, Konkuk University, Seoul 143-701, Korea. synah@konkuk.ac.kr
- Publication Type:Original Article
- Keywords:
GABAC receptor;
Ligand-gated ion channel;
Resveratrol;
Xenopus oocyte
- MeSH:
Fruit;
gamma-Aminobutyric Acid;
Humans;
Inhibitory Concentration 50;
Ligand-Gated Ion Channels;
Nervous System;
Oocytes;
Receptors, GABA;
Retinal Bipolar Cells;
RNA, Complementary;
Sesquiterpenes;
Stilbenes;
Vitis;
Wine;
Xenopus
- From:The Korean Journal of Physiology and Pharmacology
2013;17(2):175-180
- CountryRepublic of Korea
- Language:English
-
Abstract:
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-HT3A receptors. The gamma-aminobutyric acidC (GABAC) 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 GABAC receptor expressed in Xenopus oocytes injected with cRNA encoding human GABAC rho subunits. Our data show that the application of GABA elicits an inward peak current (IGABA) in oocytes that express the GABAC receptor. Resveratrol treatment had no effect on oocytes injected with H2O or with GABAC receptor cRNA. Co-treatment with resveratrol and GABA inhibited IGABA in oocytes with GABAC receptors. The inhibition of IGABA by resveratrol was in a reversible and concentration-dependent manner. The IC50 of resveratrol was 28.9+/-2.8 microM in oocytes expressing GABAC receptor. The inhibition of IGABA by resveratrol was in voltage-independent and non-competitive manner. These results indicate that resveratrol might regulate GABAC receptor expression and that this regulation might be one of the pharmacological actions of resveratrol on the nervous system.
