Levin J, Zumoff B, Fukushima D K
J Clin Endocrinol Metab. 1978 Oct;47(4):845-9. doi: 10.1210/jcem-47-4-845.
[14C]Cortisol was injected iv into three subjects during a control period and while receiving metyrapone. The plasma kinetics of the tracer cortisol and the patterns of its urinary metabolites were measured. Metyrapone caused an increase in the volume of distribution of cortisol (34%) and in the MCR (75%); the half-life was decreased by 25%. There were marked changes in the urinary metabolite pattern: 3 alpha,11 beta,17,21-tetrahydroxy-5 alpha-pregnan-20-one, 3 alpha,17,21-trihydroxy-pregnane-11,20-dione(THE), pregnane-3 alpha,11 beta,17,20 alpha,21-pentol, plus pregnane-3 alpha,11 beta,17,20 beta-21-pentol (cortol), and 3 alpha,17,20 alpha,21-tetrahydroxypregnan-11-one (cortolone) all decreased by an average of 62%, 44%, 38%, 45%, and 25% respectively. In contrast, there was an increase of 296% in 3 alpha,17,20 beta,21-tetrahydroxypregnan-11-one (beta-cortolone). To account for these effects it is postulated that metyrapone has the following extraadrenal actions: 1) it inhibits the back reduction of cortisone to cortisol and 2) it stimulates the 20-ketosteroid reductase that converts THE to beta-cortolone.
在对照期以及服用甲吡酮期间,向三名受试者静脉注射了[14C]皮质醇。测定了示踪皮质醇的血浆动力学及其尿代谢物模式。甲吡酮使皮质醇的分布容积增加了34%,使代谢清除率增加了75%;半衰期缩短了25%。尿代谢物模式有显著变化:3α,11β,17,21-四羟基-5α-孕烷-20-酮、3α,17,21-三羟基孕烷-11,20-二酮(THE)、孕烷-3α,11β,17,20α,21-戊醇,加上孕烷-3α,11β,17,20β-21-戊醇(皮质醇)和3α,17,20α,21-四羟基孕烷-11-酮(皮质素原)分别平均下降了62%、44%、38%、45%和25%。相比之下,3α,17,20β,21-四羟基孕烷-11-酮(β-皮质素原)增加了296%。为了解释这些作用,推测甲吡酮具有以下肾上腺外作用:1)它抑制可的松向皮质醇的逆向还原,2)它刺激将THE转化为β-皮质素原的20-酮类固醇还原酶。