
pmid: 12594537
handle: 11365/18660
Several studies have indicated that quercetin promotes relaxation of vascular smooth muscle both in vivo and in vitro. However, Saponara et al. [(2002) Br J Pharmacol 135: 1819-1827] have demonstrated that quercetin is an activator of vascular L-type Ca(2+) channels.We investigated the mechanical and electrophysiological properties of quercetin and its rutoside, rutin, in an attempt to clarify how Ca(2+) channel activation might be related to the myorelaxing activity.Aorta ring preparations and single tail artery myocytes were employed for functional and patch-clamp experiments, respectively.Rutin was found to relax intact rat aorta rings, which had been precontracted with phenylephrine (pIC(50) = 5.65 +/- 0.31) but in contrast had no effect on depolarised (60 mM K(+)) preparations or on those from which the endothelium had been removed. Furthermore, rutin did not affect L-type Ca(2+) current recorded in rat tail artery myocytes. The quercetin-induced relaxation of intact rings precontracted with phenylephrine exhibited two components characterised by 6.23 +/- 0.38 and 4.66 +/- 0.09 pIC(50), respectively. Removal of the endothelium abolished the first component, leaving the second unaltered. Moreover, quercetin was found to relax 60 mM K(+) depolarised rings with a pIC(50) of 4.59 +/- 0.03. The application of quercetin in isolated smooth muscle cells brought about a marked increase of L-type Ca(2+) current (pEC(50) = 5.09 +/- 0.05). Unlike quercetin, Bay K 8644 contracted aorta rings preincubated with 10, 20 or 30 mM K(+). The myotonic effect of Bay K 8644 was observed both in the absence or presence of 30 microM quercetin. The application of Bay K 8644 (10-100 nM) caused a further significant increase in L-type Ca(2+) current in rat tail artery myocytes stimulated with 30 microM quercetin.Quercetin is a naturally occurring L-type Ca(2+) channel agonist. This effect, however, is overwhelmed by quercetin-induced vasorelaxation taking place via pathways which are more relevant than L-type Ca(2+) influx in the hierarchy of functional competencies.
Male, Patch-Clamp Techniques, Potassium Channels, Calcium Channels, L-Type, Dose-Response Relationship, Drug, Rutin, Vasodilator Agents, 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester, Muscle, Smooth, Vascular, Rats, Rat vascular smooth muscle, Electrophysiology, Vasodilation, Calcium Channel Agonists, Patch-clamp; Quercetin; Rat vascular smooth muscle; Rutin; Wine polyphenols, Animals, Wine polyphenols, Quercetin, Rats, Wistar, Patch-clamp, Aorta
Male, Patch-Clamp Techniques, Potassium Channels, Calcium Channels, L-Type, Dose-Response Relationship, Drug, Rutin, Vasodilator Agents, 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester, Muscle, Smooth, Vascular, Rats, Rat vascular smooth muscle, Electrophysiology, Vasodilation, Calcium Channel Agonists, Patch-clamp; Quercetin; Rat vascular smooth muscle; Rutin; Wine polyphenols, Animals, Wine polyphenols, Quercetin, Rats, Wistar, Patch-clamp, Aorta
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