Akademik Veri Yönetim Sistemi
VASCULAR PHARMACOLOGY, cilt.44, sa.4, ss.231-237, 2006 (SCI-Expanded)
Resveratrol causes endothelium dependent and independent relaxation of vascular smooth muscle. This study investigated the mechanisms behind the effect of resveratrol on vascular tone. Resveratrol (0.1 mM) inhibited KCI-stimulated contractions in endothelium-denuded rat aorta and this inhibition was not reversed by tetraethylamrnonium (TEA) (5 mM), glyburide (3 mu M), ouabain (0.1 mM), thapsigargin (1 mu M), or indomethacin (10 mu M). KCI (90 mM) increased the intracellular free calcium concentration ([Ca2+],) in the isolated smooth muscle cells from the rat aorta and resveratrol (0.1 mM) did not inhibit the KCI-stimulated [Ca2+](i) increase. The CaCl2- (0.1 - 100 mu M) stimulated contractions were inhibited by resveratrol (0.1 mM) in the Triton X-100 skinned smooth muscle of the aorta. In heart valve endothelium, resveratrol (0.1 mM) augmented the acetylcholine (10 mu M) stimulated [Ca2+](i) increase. Resveratrol-induced augmentation of the acetylcholine-stimulated [Ca2+](i) elevation was reversed by glyburide (3 mu M), but not by TEA (5 mM). The present study indicated that resveratrol affected vascular smooth muscle and endothelium in different ways. Resveratrol decreased the Ca2+ sensitivity but did not affect the KCI-stimulated [Ca2+](i) increase in the vascular smooth muscle. In the endothelial cells, resveratrol enhanced the agonist-stimulated [Ca2+](i) increase that might trigger nitric oxide synthesis from endothelial cells. (c) 2006 Elsevier Inc. All rights reserved.