REDUCTION OF 3-OXOSTEROIDS IN HUMAN LIVER MICROSOMES
- 1 February 1976
- journal article
- research article
- Published by Oxford University Press (OUP) in Acta Endocrinologica
- Vol. 81 (2) , 530-536
- https://doi.org/10.1530/acta.0.0810530
Abstract
The 3α- and 3β-reduction of the following steroids was studied in human liver microsomes: 5α-androstane-3,17-dione, 17β-hydroxy-5α-androstan-3-one, 5α-pregnane-3,20-dione, 5β-pregnane-3,20-dione, 3-oxo-5β-cholanoic acid and 7α-hydroxy-5α-cholestan-3-one. With NADH as cofactor there was a preferential 3α-reduction of the C19- and C21-3-oxo-steroids and a preferential 3β-reduction of the C24- and C27-3-oxo-steroids. Substitution of NADH with NADPH influenced reduction of the substrates in different ways, indicating the presence of several 3α- and 3β-hydroxysteroid dehydrogenases with different substrate specificity and specificity towards NADH and NADPH. Only small or insignificant sex differences could be observed in the reductions studied.This publication has 2 references indexed in Scilit:
- Biosynthesis of cholestanol: 5α-cholestan-3-one reductase of rat liverJournal of Lipid Research, 1966
- FURTHER STUDIES ON THE SEX DIFFERENCE IN 3²-HYDROXYSTEROID DEHYDROGENASE ACTIVITY OF RAT LIVERS1Endocrinology, 1961