Brown R D, Strott C A, Liddle G W
J Clin Invest. 1972 Jun;51(6):1413-8. doi: 10.1172/JCI106937.
Studies were undertaken to determine what part of the aldosterone biosynthetic pathway is stimulated by angiotensin and potassium. The availability of a method for isolating the early portion of the aldosterone pathway and a new method for measuring plasma deoxycorticosterone permitted the design of experiments to determine whether angiotensin and potassium stimulate the pathway before deoxycorticosterone. To eliminate ACTH-dependent steroid synthesis, the experiments were performed in subjects receiving constant dosage of dexamethasone. To minimize the intra-adrenal conversion of deoxycorticosterone to corticosterone, all subjects also received constant dosage of metyrapone. Plasma deoxycortisol was measured as an index of the activity of the zona fasciculata. In the absence of changes in plasma deoxycortisol, one may infer that changes in plasma deoxycorticosterone represent changes in function of zona glomerulosa, the site of aldosterone formation. Under these conditions, human subjects responded both to angiotensin and to potassium with significant increases in plasma deoxycorticosterone but without significant increases in plasma deoxycortisol. In contrast, small doses of ACTH given under similar conditions never induced increases in plasma deoxycorticosterone without simultaneously inducing large increases in plasma deoxycortisol. It is concluded that the aldosterone-stimulating effects of angiotensin and potassium are, at least in part, consequences of stimulation of the biosynthetic pathway at some point before the formation of deoxycorticosterone so as to increase the availability of aldosterone precursors.
开展了多项研究以确定醛固酮生物合成途径的哪个部分受到血管紧张素和钾的刺激。一种用于分离醛固酮途径早期部分的方法以及一种测量血浆脱氧皮质酮的新方法的出现,使得能够设计实验来确定血管紧张素和钾是否在脱氧皮质酮之前刺激该途径。为消除促肾上腺皮质激素(ACTH)依赖性类固醇合成,实验在接受恒定剂量地塞米松的受试者中进行。为尽量减少肾上腺内脱氧皮质酮向皮质酮的转化,所有受试者还接受了恒定剂量的甲吡酮。测量血浆脱氧皮质醇作为束状带活性的指标。在血浆脱氧皮质醇无变化的情况下,可以推断血浆脱氧皮质酮的变化代表醛固酮形成部位——球状带功能的变化。在这些条件下,人类受试者对血管紧张素和钾的反应均为血浆脱氧皮质酮显著增加,但血浆脱氧皮质醇无显著增加。相比之下,在类似条件下给予小剂量ACTH时,从未在不同时诱导血浆脱氧皮质醇大幅增加的情况下诱导血浆脱氧皮质酮增加。得出的结论是,血管紧张素和钾对醛固酮的刺激作用至少部分是在脱氧皮质酮形成之前的某个点刺激生物合成途径,从而增加醛固酮前体可用性的结果。