Hammar M, Berg A A, Kjessler B
Arch Androl. 1985;14(1):21-8. doi: 10.3109/01485018508987274.
The in vitro conversion of tritiated pregnenolone and progesterone was studied in testicular tissue from three infertile adult males before and during 25-30 weeks of therapy with hCG alone or combined with hMG. Furthermore, the in vitro conversion of pregnenolone was studied in testicular tissue from five prepubertal boys with undescended testes, two of whom had been subjected to hCG treatment for 5 weeks. The gonadotrophic treatment appeared to augment the steroid conversion mediated by the enzymes 3 beta-hydroxysteroid dehydrogenase and 17 alpha-hydroxylase in adult as well as prepubertal testicular tissue. The conversion mediated by C17-20-lyase along the delta 4 metabolic pathway was not increased, causing a "trap" along the delta 4 metabolic pathway. The increased production of testosterone in vitro from tritiated pregnenolone, which was observed during gonadotrophic treatment, probably took place along the delta 5 metabolic pathway through the C17-20-lyase step, whereas C21 steroids converted to the delta 4 metabolic pathway were found to be "trapped" as 17 alpha-hydroxyprogesterone.
研究了3名成年不育男性在单独使用hCG或联合使用hMG治疗25 - 30周之前及期间,其睾丸组织中氚化孕烯醇酮和孕酮的体外转化情况。此外,还研究了5名青春期前隐睾男孩睾丸组织中孕烯醇酮的体外转化情况,其中2名男孩接受了5周的hCG治疗。促性腺激素治疗似乎增强了成年及青春期前睾丸组织中由3β-羟基类固醇脱氢酶和17α-羟化酶介导的类固醇转化。沿δ4代谢途径由C17 - 20裂解酶介导的转化未增加,导致沿δ4代谢途径出现“滞留”现象。在促性腺激素治疗期间观察到的由氚化孕烯醇酮体外产生睾酮的增加,可能是沿δ5代谢途径通过C17 - 20裂解酶步骤发生的,而转化为δ4代谢途径的C21类固醇则被“滞留”为17α-羟孕酮。