Nicorandil-induced ATP release in endothelial cells of rat caudal artery is associated with increase in intracellular Ca2+

Citation
M. Hashimoto et al., Nicorandil-induced ATP release in endothelial cells of rat caudal artery is associated with increase in intracellular Ca2+, EUR J PHARM, 416(3), 2001, pp. 179-183
Citations number
20
Categorie Soggetti
Pharmacology & Toxicology
Journal title
EUROPEAN JOURNAL OF PHARMACOLOGY
ISSN journal
00142999 → ACNP
Volume
416
Issue
3
Year of publication
2001
Pages
179 - 183
Database
ISI
SICI code
0014-2999(20010330)416:3<179:NARIEC>2.0.ZU;2-4
Abstract
The effect of nicorandil, an ATP-sensitive K+ channel opener, on the level of intracellular Ca2+ ([Ca2+](i)) and on ATP release in endothelial cells o f the rat caudal artery was examined using a fluorescent confocal microscop ic imaging system and high-performance liquid chromatography (HPLC) with fl uorescent detection, respectively. Nicorandil significantly increased [Ca2](i) and the overflow of ATP and its metabolites. The former reaction was a bolished in the absence of extracellular Ca2+, but it did not change in the presence of thapsigargin or cycIopiazonic acid. The increase in the overfl ow of ATP and [Ca2+](i) induced by nicorandil was markedly suppressed by gl ibenclamide, an ATP-sensitive K+ channel blocker. The increase of [Ca2+](i) induced by nicorandil was significantly and inversely correlated with the level of intracellular ATP in the endothelial cells, suggesting that activa tion of ATP-sensitive K+ channels by nicorandil increases Ca2+ influx in en dothelial cells. The increase of [Ca2+](i) might be associated with ATP rel ease. (C) 2001 Elsevier Science B.V. All rights reserved.