Resveratrol Inhibits GABAC 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 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 γ-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 ρ 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 µM 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.

[1]  F. Bloom,et al.  Localizing 3H-GABA in Nerve Terminals of Rat Cerebral Cortex by Electron Microscopic Autoradiography , 1971, Nature.

[2]  P. Taylor,et al.  Local anesthetics and histrionicotoxin are allosteric inhibitors of the acetylcholine receptor. Studies of clonal muscle cells. , 1982, The Journal of biological chemistry.

[3]  J. Changeux,et al.  Multiple sites of action for noncompetitive blockers on acetylcholine receptor rich membrane fragments from torpedo marmorata. , 1983, Biochemistry.

[4]  R. Weatherby,et al.  Bicuculline-insensitive GABA receptors: Studies on the binding of (−)-baclofen to rat cerebellar membranes , 1984, Neuroscience Letters.

[5]  J. Wamsley,et al.  Autoradiographic localization of subcomponents of the macromolecular GABA receptor complex. , 1986, Life Science.

[6]  E. Cherubini,et al.  Transient expression of a novel type of GABA response in rat CA3 hippocampal neurones during development. , 1994, Journal of Physiology.

[7]  H. Arias Luminal and non-luminal non-competitive inhibitor binding sites on the nicotinic acetylcholine receptor. , 1996, Molecular membrane biology.

[8]  H. Wässle,et al.  Glycine and GABA receptors in the mammalian retina , 1998, Vision Research.

[9]  J. Bormann,et al.  The 'ABC' of GABA receptors. , 2000, Trends in pharmacological sciences.

[10]  H. Scherübl,et al.  GABAC receptors in neuroendocrine gut cells: a new GABA-binding site in the gut , 2000, Pflügers Archiv.

[11]  G. Tramu,et al.  Molecular and Electrophysiological Evidence for a GABAC Receptor in Thyrotropin-Secreting Cells. , 2000, Endocrinology.

[12]  G. Johnston,et al.  GABA-Activated ligand gated ion channels: medicinal chemistry and molecular biology. , 2000, Journal of medicinal chemistry.

[13]  M. Chan Antimicrobial effect of resveratrol on dermatophytes and bacterial pathogens of the skin. , 2002, Biochemical pharmacology.

[14]  P. Lukasiewicz,et al.  Elimination of the ρ1 Subunit Abolishes GABACReceptor Expression and Alters Visual Processing in the Mouse Retina , 2002, The Journal of Neuroscience.

[15]  J. Hanrahan,et al.  GABA(C) receptors as drug targets. , 2003, Current drug targets. CNS and neurological disorders.

[16]  S. Pervaiz Resveratrol: from grapevines to mammalian biology , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[17]  J. Deuchars,et al.  Evidence for Inhibition Mediated by Coassembly of GABAA and GABAC Receptor Subunits in Native Central Neurons , 2004, The Journal of Neuroscience.

[18]  M. Chebib GABAC RECEPTOR ION CHANNELS , 2004, Clinical and experimental pharmacology & physiology.

[19]  P. Langcake,et al.  A new class of phytoalexins from grapevines , 1977, Experientia.

[20]  L. Mucke,et al.  SIRT1 Protects against Microglia-dependent Amyloid-β Toxicity through Inhibiting NF-κB Signaling* , 2005, Journal of Biological Chemistry.

[21]  L. Mucke,et al.  SIRT1 protects against microglia-dependent amyloid-beta toxicity through inhibiting NF-kappaB signaling. , 2005, The Journal of biological chemistry.

[22]  A. Schousboe,et al.  Charge selectivity of the Cys‐loop family of ligand‐gated ion channels , 2005, Journal of neurochemistry.

[23]  M. Perez-Pinzon,et al.  Resveratrol Mimics Ischemic Preconditioning in the Brain , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  Antonino Cattaneo,et al.  Resveratrol Prolongs Lifespan and Retards the Onset of Age-Related Markers in a Short-Lived Vertebrate , 2006, Current Biology.

[25]  D. Holtzman,et al.  Pomegranate Polyphenols and Resveratrol Protect the Neonatal Brain against Hypoxic-Ischemic Injury , 2007, Developmental Neuroscience.

[26]  Y. Toyohira,et al.  Dual effects of daidzein, a soy isoflavone, on catecholamine synthesis and secretion in cultured bovine adrenal medullary cells. , 2007, Endocrinology.

[27]  Y. Toyohira,et al.  Effects of resveratrol, a grape polyphenol, on catecholamine secretion and synthesis in cultured bovine adrenal medullary cells. , 2007, Biochemical pharmacology.

[28]  Qi Xu,et al.  Protective Effect of Resveratrol against Kainate-induced Temporal Lobe Epilepsy in Rats , 2009, Neurochemical Research.

[29]  D. Das,et al.  Resveratrol, a unique phytoalexin present in red wine, delivers either survival signal or death signal to the ischemic myocardium depending on dose. , 2009, The Journal of nutritional biochemistry.

[30]  T. Saleh,et al.  Resveratrol preconditioning induces cellular stress proteins and is mediated via NMDA and estrogen receptors , 2010, Neuroscience.

[31]  Sun-Hye Choi,et al.  Resveratrol enhances 5-hydroxytryptamine type 3A receptor-mediated ion currents: the role of arginine 222 residue in pre-transmembrane domain I. , 2011, Biological & pharmaceutical bulletin.

[32]  Byung-Hwan Lee,et al.  Inhibitory Effects of Quercetin on Muscle-type of Nicotinic Acetylcholine Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes. , 2011, The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology.