McInnes G T, Shelton J R, Asbury M J, Harrison I R, Clarke J M, Ramsay L E, Venning G R
Clin Pharmacol Ther. 1981 Aug;30(2):218-25. doi: 10.1038/clpt.1981.151.
The renal antimineralocorticoid activity of single oral doses of a new aldosterone antagonist OH OPC(ME)-K was compared to that of spironolactone in two studies in healthy men. OH OPC(ME)-K reversed the urinary electrolyte response to fludrocortisone in the period up to 16 hr after treatment, but it was less potent than spironolactone on a weight basis. The best estimate of the relative potency of OH OPC(ME)-K: spironolactone (derived from a simple protocol using equal single doses of the two drugs) was 0.60:1 (95% confidence limits 0.24:1 to 1.42:1), in good agreement with the estimate from a more complex three-dose parallel-line bioassay (0.61:1, 95% confidence limits 0.48:1 to 0.79:1). The results of simple single-dose studies can be used, with certain assumptions, to provide a useful estimate of the relative potency of new aldosterone antagonists at an early stage of development.
在两项针对健康男性的研究中,比较了单次口服新型醛固酮拮抗剂OH OPC(ME)-K与螺内酯的肾脏抗盐皮质激素活性。在治疗后的16小时内,OH OPC(ME)-K逆转了氟氢可的松引起的尿液电解质反应,但按重量计算其效力低于螺内酯。OH OPC(ME)-K与螺内酯的相对效力最佳估计值(源自使用两种药物等单剂量的简单方案)为0.60:1(95%置信限为0.24:1至1.42:1),与更复杂的三剂量平行线生物测定法的估计值(0.61:1,95%置信限为0.48:1至0.79:1)高度一致。简单的单剂量研究结果在某些假设条件下,可用于在开发早期阶段对新型醛固酮拮抗剂的相对效力提供有用的估计。