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血管紧张素转换酶和中性内肽酶抑制剂的作用:缓激肽的影响。

Effects of angiotensin-converting enzyme and neutral endopeptidase inhibitors: influence of bradykinin.

作者信息

Pham I, Gonzalez W, Doucet J, Fournie-Zaluski M C, Roques B P, Michel J B

机构信息

INSERM U 367, Paris, France.

出版信息

Eur J Pharmacol. 1996 Feb 5;296(3):267-76. doi: 10.1016/0014-2999(95)00706-7.

Abstract

These experiments compare the effects of a neutral endopeptidase inhibitor, retrothiorphan, 1-[(1-mercaptomethyl-2-phenyl)ethyl]amino-1-oxopropanoic acid, a converting enzyme inhibitor, enalaprilat, and the combination of the two inhibitors on changes in blood pressure and renal function induced by exogenous and endogenous bradykinin in deoxycorticosterone acetate (DOCA)-salt rats. Enalaprilat potentiated the exogenous bradykinin-induced hypotensive responses while retrothiorphan potentiated the effects on urinary cyclic-GMP (cGMP) and bradykinin. The combination potentiated the exogenous bradykinin-induced hypotensive effects and the bradykinin-induced urinary excretion of cGMP, bradykinin and prostaglandin. The bradykinin B2 receptor antagonist, Hoe 140, had no effect on the enalaprilat- and retrothiorphan-induced changes in blood pressure and renal function. In conclusion, while angiotensin-converting enzyme and neutral endopeptidase are involved in the vascular and renal catabolism of exogenous bradykinin, the effects of the peptidase inhibitors do not appear to depend on the protection of endogenous bradykinin under acute conditions in DOCA-salt rats.

摘要

这些实验比较了一种中性内肽酶抑制剂(雷托硫因,1-[(1-巯基甲基-2-苯基)乙基]氨基-1-氧代丙酸)、一种转化酶抑制剂(依那普利拉)以及这两种抑制剂联合使用,对醋酸脱氧皮质酮(DOCA)-盐大鼠中外源性和内源性缓激肽诱导的血压和肾功能变化的影响。依那普利拉增强了外源性缓激肽诱导的降压反应,而雷托硫因增强了对尿中环磷酸鸟苷(cGMP)和缓激肽的影响。联合使用增强了外源性缓激肽诱导的降压作用以及缓激肽诱导的cGMP、缓激肽和前列腺素的尿排泄。缓激肽B2受体拮抗剂Hoe 140对依那普利拉和雷托硫因诱导的血压和肾功能变化没有影响。总之,虽然血管紧张素转化酶和中性内肽酶参与外源性缓激肽的血管和肾脏代谢,但在DOCA-盐大鼠急性条件下,肽酶抑制剂的作用似乎并不依赖于对内源性缓激肽的保护。

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