In vivo androgen retention in mouse kidney.

Abstract:

:The in vivo retention of 3-H-testosterone, dihydrotestosterone (DHT), 3alpha-androstanediol (3alpha-DIOL), 3beta-DIOL, androstenedione, progesterone and cortisol by renal cytoplasm and nuclei of male and female mice was studied. Testosterone was the major androgen isolated from cytoplasm and nuclei following testosterone or androstenedione administration. By contrast, DHT was the major intracellular androgen after DHT, 3alpha- or 3beta-DIOL injection. The uptake of 3-H-testosterone or 3-H-DHT was abolished by excess unlabeled testosterone, DHT or cyproterone acetate. Androgen concentrations in kidney fractions from female mice were similar to those from males. There was no appreciable concentration of the isolated steroids following 3-H-progesterone administration. 3H-cortisol was concentrated in both cytoplasm and nuclei but was not displaced by non-radioactive androgens. These findings suggest that in contrast to prostate, mouse kidney can concentrate both testosterone and DHT. However, since testosterone is the major androgen in blood and since it is not metabolized in kidney, it is the major effector androgen in this organ. Androstenedione is active via conversion to testosterone while DIOLS are androgenic via metabolism to DHT.

journal_name

Steroids

journal_title

Steroids

authors

Bullock LP,Bardin CW

doi

10.1016/s0039-128x(75)80011-0

subject

Has Abstract

pub_date

1975-01-01 00:00:00

pages

107-19

issue

1

eissn

0039-128X

issn

1878-5867

pii

S0039-128X(75)80011-0

journal_volume

25

pub_type

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