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Neuroprotective abilities of resveratrol and other red wine constituents against nitric oxide‐related toxicity in cultured hippocampal neurons
Author(s) -
Bastianetto Stéphane,
Zheng WenHua,
Quirion Rémi
Publication year - 2000
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0703626
Subject(s) - nitric oxide , sodium nitroprusside , neuroprotection , quercetin , resveratrol , chemistry , biochemistry , pharmacology , catechin , antioxidant , nitric oxide synthase , neurotoxicity , toxicity , trolox , polyphenol , biology , enzyme , organic chemistry , dpph
Animal and epidemiological studies suggest that polyphenol constituents of red wine possess antioxidant activities that favour protection against cardiovascular disease – the so‐called. ‘French paradox’ – and possibly, central nervous system disorders such as Alzheimer's disease (AD) and ischaemia. In the present study, the potential of three major red wine derived‐polyphenols to protect against toxicity induced by the nitric oxide free radical donors sodium nitroprusside (SNP) and 3‐morpholinosydnonimine (SIN‐1) was examined in cultured rat hippocampal cells. Both co‐ and post‐treatments with either the stilbene resveratrol (5–25 μ M ) or the flavonoids quercetin (5–25 μ M ) and (+)‐catechin (1–10 μ M ) were capable of attenuating hippocampal cell death and intracellular reactive oxygen species accumulation produced by SNP (100 μ M and 1 m M , respectively). However, among the phenolic compounds tested, only the flavonoids afforded significant protection against 5 m M SIN‐1‐induced toxicity. The effects of phenolic constituents were shared by Trolox (100 μ M ), a vitamin E analogue, but not by selective inhibitors of cyclo‐oxygenases (COX) and lipoxygenases (LOX). Among the phenolic compounds tested, only quercetin (10 μ M ) inhibited 100 μ M SNP‐stimulated protein kinase C (PKC) activation, whereas none of them were able to attenuate nitrite accumulation caused by SNP (100 μ M ). Taken together, these data suggest that the neuroprotective abilities of quercetin, resveratrol, and (+)‐catechin result from their antioxidant properties rather than their purported inhibitory effects on intracellular enzymes such as COX, LOX, or nitric oxide synthase. Quercetin, however, may also act via PKC to produce its protective effects.British Journal of Pharmacology (2000) 131 , 711–720; doi: 10.1038/sj.bjp.0703626