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清醒大鼠中心血管效应、尼可地尔血浆水平与血管cGMP生成的相互关系

Interrelationship of cardiovascular effects, plasma levels of nicorandil, and vascular cGMP formation in conscious rats.

作者信息

Sakai K, Akima M, Kamachi S, Moriyasu M, Kitajima S

机构信息

Central Research Laboratories, Chugai Pharmaceutical Co., Ltd, Tokyo, Japan.

出版信息

J Pharm Pharmacol. 1998 Jun;50(6):661-6. doi: 10.1111/j.2042-7158.1998.tb06902.x.

Abstract

The relationship between the dual activity of nicorandil (KATP channel-opening activity and nitrate-like action), plasma levels, and changes in vascular cGMP levels and cardiovascular parameters was investigated in conscious rats. Nicorandil (3 mg kg(-1), p.o.) was rapidly absorbed and caused a significant reduction in blood pressure, lasting for at least 1 h, increases in heart rate and femoral blood flow, and decreases in femoral vascular resistance. These were entirely abolished by intravenous glibenclamide (20 mg kg(-1)). The plasma concentration of nicorandil reached a maximum 30 min after dosing. After administration of nicorandil, a correlation was observed between blood pressure and plasma nicorandil level or femoral vascular resistance. A significant increase (P < 0.05) in the cGMP content of the thoracic aorta occurred 15 min after administration of nicorandil, and persisted for at least 2 h. These results imply that nicorandil induces vasodilatation by opening KATP channels in peripheral resistance vessels, leading to overt reduction of blood pressure, but acts on conductance vessels mainly through nitrate-like activity.

摘要

在清醒大鼠中研究了尼可地尔的双重活性(开放KATP通道活性和类硝酸盐作用)、血浆水平以及血管cGMP水平变化和心血管参数之间的关系。尼可地尔(3 mg kg(-1),口服)吸收迅速,可使血压显著降低,持续至少1小时,使心率和股血流量增加,股血管阻力降低。静脉注射格列本脲(20 mg kg(-1))可完全消除这些作用。尼可地尔给药后30分钟血浆浓度达到峰值。给予尼可地尔后,观察到血压与血浆尼可地尔水平或股血管阻力之间存在相关性。给予尼可地尔15分钟后,胸主动脉cGMP含量显著增加(P < 0.05),并持续至少2小时。这些结果表明,尼可地尔通过开放外周阻力血管中的KATP通道诱导血管舒张,导致血压明显降低,但主要通过类硝酸盐活性作用于传导血管。

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