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去甲肾上腺素、甲氧明和去氧肾上腺素对大鼠肾皮质切片肾素释放的抑制作用。

Inhibitory effects of norepinephrine, methoxamine and phenylephrine on renin release from rat kidney cortical slices.

作者信息

Matsumura Y, Miyawaki N, Sasaki Y, Morimoto S

出版信息

J Pharmacol Exp Ther. 1985 Jun;233(3):782-7.

PMID:2989497
Abstract

We attempted to determine whether the inhibition of renin release from rat kidney cortical slices by alpha adrenoceptor agonists is mediated by activation of alpha-1 and/or alpha-2 adrenoceptors, and to investigate the role of calcium in the mechanisms of this inhibition. Norepinephrine (NE), methoxamine (ME) and phenylephrine (PE) produced a concentration-dependent inhibition of renin release from rat kidney cortical slices, whereas clonidine was without effect. NE-, ME- and PE-induced inhibition of renin release was blocked by prazosin, which was 2 or 3 orders of magnitude more potent than yohimbine. The inhibitory effects of NE, ME and PE on renin release from the slices were abolished by removal of calcium from the incubation medium. Calcium antagonists, verapamil and nifedipine, attenuated the responses of renin release to NE, ME and PE, in a concentration-dependent manner. The inhibitory effects of NE, ME and PE on renin release were blocked significantly by N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide, a calmodulin antagonist, but not by N-(6-aminohexyl)-1-naphthalenesulfonamide, which has virtually no calmodulin antagonistic activity. These findings suggest that alpha adrenoceptor agonists inhibit renin release from rat kidney cortical slices mainly via alpha-1 adrenoceptors and that calcium influx followed by the activation of the calcium-calmodulin system is involved in the above inhibition.

摘要

我们试图确定α肾上腺素能受体激动剂对大鼠肾皮质切片肾素释放的抑制作用是否由α1和/或α2肾上腺素能受体的激活介导,并研究钙在这种抑制机制中的作用。去甲肾上腺素(NE)、甲氧明(ME)和去氧肾上腺素(PE)对大鼠肾皮质切片的肾素释放产生浓度依赖性抑制,而可乐定则无此作用。NE、ME和PE诱导的肾素释放抑制被哌唑嗪阻断,哌唑嗪的效力比育亨宾强2或3个数量级。从孵育培养基中去除钙后,NE、ME和PE对切片肾素释放的抑制作用消失。钙拮抗剂维拉帕米和硝苯地平以浓度依赖性方式减弱肾素释放对NE、ME和PE的反应。钙调蛋白拮抗剂N-(6-氨基己基)-5-氯-1-萘磺酰胺可显著阻断NE、ME和PE对肾素释放的抑制作用,但几乎没有钙调蛋白拮抗活性的N-(6-氨基己基)-1-萘磺酰胺则无此作用。这些发现表明,α肾上腺素能受体激动剂主要通过α1肾上腺素能受体抑制大鼠肾皮质切片的肾素释放,且上述抑制作用涉及钙内流后钙-钙调蛋白系统的激活。

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