Provencher P H, Tremblay Y, Bélanger A
CHUL Research Center, Quebec, Canada.
J Endocrinol. 1992 Feb;132(2):269-76. doi: 10.1677/joe.0.1320269.
The present study examined the effects of steroids on steroidogenic enzyme activity in adrenal glands. Guinea-pig fasciculata-glomerulosa (FG) cells maintained in primary culture were exposed to steroids for 48 h. Although the treatment with androstenedione alone had no effect on 3 beta-hydroxysteroid dehydrogenase 4-ene-5-ene-isomerase (3 beta-HSD), 17-hydroxylase and 17,20-lyase activities, there was inhibition of 11-hydroxylase and 21-hydroxylase activities. When FG cells were exposed to 10 nmol ACTH/l for the last 24 h of incubation, ACTH alone had no effect on steroidogenic enzymes but, while combined with androstenedione, it further decreased 21-hydroxylase activity and stimulated 17-hydroxylase and 17,20-lyase activities. Cortisol, corticosterone, oestradiol and 11 beta-hydroxy androstenedione had no effect on steroidogenic enzyme activities while the inhibitory effect on 21-hydroxylase activity was only observed with androstenedione, testosterone and dihydrotestosterone. Addition of hydroxyflutamide, a pure antiandrogen, did not block the inhibitory effect of androstenedione on 21-hydroxylase and 11-hydroxylase activities. The reduction in oxygen tension from 19 to 2% which was aimed at examining the oxygen-mediated effects on steroidogenic enzymes, revealed that the reduction in 21-hydroxylase activity induced by androstenedione could not be prevented by low oxygen tension. An interaction of C19 steroids at the level of the enzymes is also suggested by our finding that androstenedione had no effect on basal and ACTH-stimulated steady-state 11-hydroxylase, 17-hydroxylase, 17,20-lyase and 21-hydroxylase mRNA levels.(ABSTRACT TRUNCATED AT 400 WORDS)
本研究检测了类固醇对肾上腺中类固醇生成酶活性的影响。将原代培养的豚鼠束状带-球状带(FG)细胞暴露于类固醇48小时。虽然单独用雄烯二酮处理对3β-羟基类固醇脱氢酶4-烯-5-烯异构酶(3β-HSD)、17-羟化酶和17,20-裂解酶活性没有影响,但11-羟化酶和21-羟化酶活性受到抑制。当FG细胞在孵育的最后24小时暴露于10 nmol促肾上腺皮质激素/升时,单独的促肾上腺皮质激素对类固醇生成酶没有影响,但是,与雄烯二酮联合使用时,它进一步降低了21-羟化酶活性,并刺激了17-羟化酶和17,20-裂解酶活性。皮质醇、皮质酮、雌二醇和11β-羟基雄烯二酮对类固醇生成酶活性没有影响,而仅在雄烯二酮、睾酮和双氢睾酮作用下观察到对21-羟化酶活性的抑制作用。添加纯抗雄激素药物氟他胺并不能阻断雄烯二酮对21-羟化酶和11-羟化酶活性的抑制作用。将氧张力从19%降至2%以检测氧对类固醇生成酶的介导作用,结果显示低氧张力无法阻止雄烯二酮诱导的21-羟化酶活性降低。我们发现雄烯二酮对基础和促肾上腺皮质激素刺激的稳态11-羟化酶、17-羟化酶、17,20-裂解酶和21-羟化酶mRNA水平没有影响,这也提示了C19类固醇在酶水平上存在相互作用。(摘要截选至400字)