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Kappa-opioid receptor stimulation contributes to aortic artery dilation through activation of K(ATP) channel in the rats / 生理学报
Acta Physiologica Sinica ; (6): 91-95, 2003.
Article in English | WPRIM | ID: wpr-318936
ABSTRACT
To investigate the relaxation effect and underlying mechanism of U50,488H (a selective kappa-opioid receptor agonist) on aorta in the rat, isolated aortic ring was perfused and the tension of the vessel was measured. It was shown (1) kappa-opioid receptor stimulation with U50,488H relaxed rat aorta dose-dependently; (2) the relaxation effect of U50,488H on aorta was partially endothelium-dependent; (3) the relaxation effect of U50,488H was significantly attenuated in the presence of glybenclamide and glipizide, two ATP-sensitive K(+) channel (K(ATP)) blockers; and (4) the relaxation effect of U50,488H on vessel bore no relationship to muscarinic-receptor, beta-adrenoceptor, prostaglandin and nitric oxide (NO). These results indicate that kappa-opioid receptor stimulation with U50,488H relaxes the aortic artery at least partially via K(ATP) channel in the rat.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Aorta / Pharmacology / Physiology / Vasodilation / In Vitro Techniques / Rats, Sprague-Dawley / Receptors, Opioid, kappa / 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer / KATP Channels / Metabolism Limits: Animals Language: English Journal: Acta Physiologica Sinica Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Aorta / Pharmacology / Physiology / Vasodilation / In Vitro Techniques / Rats, Sprague-Dawley / Receptors, Opioid, kappa / 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer / KATP Channels / Metabolism Limits: Animals Language: English Journal: Acta Physiologica Sinica Year: 2003 Type: Article