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正常志愿者中马来酸依那普利与赖氨酸类似物(MK-521);血浆药物水平与肾素-血管紧张素系统之间的关系

Enalapril maleate and a lysine analogue (MK-521) in normal volunteers; relationship between plasma drug levels and the renin angiotensin system.

作者信息

Biollaz J, Schelling J L, Jacot Des Combes B, Brunner D B, Desponds G, Brunner H R, Ulm E H, Hichens M, Gomez H J

出版信息

Br J Clin Pharmacol. 1982 Sep;14(3):363-8. doi: 10.1111/j.1365-2125.1982.tb01992.x.

Abstract

1 Two single doses of 10 mg each of the converting enzyme inhibitor enalapril maleate or MK-421 and of its lysine analogue (MK-521) were administered p.o. to twelve male volunteers. 2 The active diacid metabolite of MK-421 and the lysine analogue were determined by radioimmunoassay and MK-421 by the active metabolite method following in vitro hydrolysis. 3 Peak serum levels of MK-421, active metabolite and lysine analogue were reached within 1, 3 to 4, and 6 h respectively. Practically all MK-421 had disappeared from serum within 4 h. 4 A close correlation between percent inhibition of plasma converting enzyme activity and the serum concentration of active metabolite was observed ( r = 0.98, n = 171, P less than 0.001). Similarly, converting enzyme blockade as expressed by the ratio plasma angiotensin II/angiotensin I was closely correlated with serum active metabolite levels (r = 0.93, n = 15, P less than 0.001).

摘要
  1. 给12名男性志愿者口服单剂量10毫克的转化酶抑制剂马来酸依那普利(MK - 421)及其赖氨酸类似物(MK - 521)。

  2. MK - 421的活性二酸代谢物及其赖氨酸类似物通过放射免疫测定法测定,MK - 421通过体外水解后的活性代谢物法测定。

  3. MK - 421、活性代谢物和赖氨酸类似物的血清峰值水平分别在1小时、3至4小时和6小时内达到。实际上,所有MK - 421在4小时内已从血清中消失。

  4. 观察到血浆转化酶活性抑制百分比与活性代谢物的血清浓度之间存在密切相关性(r = 0.98,n = 171,P < 0.001)。同样,以血浆血管紧张素II/血管紧张素I比值表示的转化酶阻断与血清活性代谢物水平密切相关(r = 0.93,n = 15,P < 0.001)。

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