17α-hydroxylase (P450c 17-20) catalyzes hydroxylation and cleavage of steroids (converts steroids from a 21-carbon to a 19-carbon molecule in Δ4 and Δ5- hydroxysteroid pathways);
Production/Activity Regulated by:
- LH
P450c17 Activity suppressed by:
- TESTOSTERONE (via effects on second messenger cAMP pathway)
17α-hydroxylase /C17-20 lyasepathway directly affected by:
- Nicotine;
- Ethanol (17α-hydroxylase)
- Drugs: Bromocriptine, Mibolerone, Danazol, Cyproterone acetate, Cyclosporin A, Flutamide.
Δ5 - hydroxy-steroid pathway |
PREGNENOLONE |
→ P450 C17 hydroxylation |
17α-Hydroxy- PREGNENOLONE |
→ P450 C17 Lyase activity cleavage |
DHEA |
Δ4 - hydroxy-steroid pathway |
PROGESTERONE |
→ P450 C17 hydroxylation |
17α-Hydroxy-PROGESTERONE |
→ P450 C20 Lyase * |
ANDRO-STENEDIONE |
•In rats, P450 C17 catalyses:
17α-HydroxyPROGESTERONE ➔ ANDROSTENEDIONE
(but not in humans, which could explain differences between rat and human studies);