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醛固酮拮抗剂在健康男性中的相对效价及构效关系:与动物实验结果的相关性

Relative potency and structure activity relationships of aldosterone antagonists in healthy man: correlation with animal experience.

作者信息

McInnes G T, Shelton J R, Ramsay L E, Harrison I R, Asbury M J, Clarke J M, Perkins R M, Venning G R

出版信息

Br J Clin Pharmacol. 1982 Mar;13(3):331-9. doi: 10.1111/j.1365-2125.1982.tb01383.x.

Abstract

1 The renal antimineralocorticoid potency of single doses of thirteen compounds with properties in animals compatible with competitive aldosterone antagonism was compared to that of spironolactone in healthy men. 2 Twelve compounds showed significant activity when compared to placebo but only one, prorenoate potassium, was significantly more potent than spironolactone on a weight basis. 3 The results allowed ranking of the compounds in order of potency relative to spironolactone and general observations on structure activity relationships in man. 4 Animal bioassays and in vitro aldosterone binding studies are unreliable predictors of the human activity of competitive mineralocorticoid antagonists.

摘要
  1. 将单剂量的13种性质与竞争性醛固酮拮抗作用相符的化合物在动物体内的肾抗盐皮质激素效力,与螺内酯在健康男性体内的效力进行了比较。2. 与安慰剂相比,12种化合物显示出显著活性,但按重量计算,只有一种,即普乐睾酮钾,比螺内酯的效力显著更强。3. 结果可以按照相对于螺内酯的效力对这些化合物进行排序,并对人体结构活性关系进行总体观察。4. 动物生物测定和体外醛固酮结合研究对于竞争性盐皮质激素拮抗剂的人体活性来说是不可靠的预测指标。

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The aldosterone blocking effects of spirolactones.螺内酯的醛固酮阻断作用。
Jpn J Pharmacol. 1962 Mar;11:77-87. doi: 10.1254/jjp.11.77.

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