REGULATION OF 21-HYDROXYLASE ACTIVITY BY STEROIDS

Citation
A. Belanger et al., REGULATION OF 21-HYDROXYLASE ACTIVITY BY STEROIDS, Endocrine research, 21(1-2), 1995, pp. 329-341
Citations number
16
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
07435800
Volume
21
Issue
1-2
Year of publication
1995
Pages
329 - 341
Database
ISI
SICI code
0743-5800(1995)21:1-2<329:RO2ABS>2.0.ZU;2-1
Abstract
In this study, we investigated the effect of steroids on guinea pig an d bovine adrenal steroidogenesis, especially 21-hydroxylase activity. Analysis of guinea pig adrenal steroids indicated the presence of high concentrations of androstenedione in the guinea pig adrenal; furtherm ore, in vitro studies using guinea pig adrenal cortex cells in primary culture confirmed that androstenedione is one of the major C19 steroi ds produced and secreted. The direct action of steroids on steroid pro duction by adrenal cells was investigated. Our data indicate that ster oids themselves increase C19 steroid synthesis and inhibit glucocortic oid production by guinea pig adrenal cells without affecting gene expr ession for steroidogenic enzymes. Incubation of a series of C19 steroi ds, namely, androstenedione, with guinea pig adrenal cell cultures dem onstrated that the decrease in 21-hydroxylase activity is largely inde pendent of the androgenic activity of C19 steroids. RU38486, a synthet ic C18 steroid possessing a 4-ene-3-ketosteroid with an aryl group at position 11 and a very low affinity for the androgen receptor, also ir reversibly altered 21-hydroxylase activity. An effect of RU38486 on 21 -hydroxylase activity was also demonstrated in bovine adrenal cells. F urther studies with bovine adrenal cells showed that the decrease in 2 1-hydroxylase activity induced by RU38486 was accompanied by a small b ut significant inhibition of P450c21 protein levels at both basal and ACTH-stimulated levels. In summary, our data indicate that alteration of 21-hydroxylase activity by steroids is likely due to a direct actio n on P540c21 protein, and the levels of androstenedione in the adrenal are high enough to inhibit 21-hydroxylase activity.