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钙离子通道阻滞剂和沙拉新对兔主动脉条中血管紧张素II诱导收缩的影响。

Effect of Ca++ channel blockers and saralasin on angiotensin II induced contraction in rabbit aortic strip.

作者信息

Kheterpal K, Lall S B, Rajdev S, Gupta Y K

出版信息

Indian J Physiol Pharmacol. 1986 Apr-Jun;30(2):166-70.

PMID:3818044
Abstract

To investigate the role of calcium in angiotensin II (A II) induced contractions in rabbit aortic strip, the action of verapamil, nifedipine, cinnarizine and saralasin was studied. The cumulative dose response curves obtained with A II shifted to right with increasing concentrations of all these four agents. The antagonism was noncompetitive. The pD'2 value of saralasin was 8.49 of nifedipine, 8.15 and or verapamil 7.92. Cinnarizine which mainly acts at intracellular site had pD'2 value 5.54. The results indicate that A II induced contractions critically depend on entry of calcium through channels which appear to be closely associated with angiotensin receptors.

摘要

为研究钙在血管紧张素II(A II)诱导的兔主动脉条收缩中的作用,研究了维拉帕米、硝苯地平、桂利嗪和沙拉新的作用。随着这四种药物浓度的增加,A II获得的累积剂量反应曲线向右移动。这种拮抗作用是非竞争性的。沙拉新的pD'2值为8.49,硝苯地平为8.15,维拉帕米为7.92。主要作用于细胞内位点的桂利嗪的pD'2值为5.54。结果表明,A II诱导的收缩关键取决于钙通过与血管紧张素受体密切相关的通道进入细胞。

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