help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marandici, A.
Right arrow Articles by Monder, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marandici, A.
Right arrow Articles by Monder, C.

Endocrinology, Vol 113, 1400-1407, Copyright © 1983 by Endocrine Society


ARTICLES

A comparison of the tissue distribution and metabolism of 11-deoxy-[1,2- 3H]corticosterone in the BALB/c and C57BL/6 strains of mice

A Marandici and C Monder

Corticosteroid side-chain isomerase of mouse liver catalyzes the reversible interconversion of the ketol and aldol configurations of the corticosteroid side chain. Activity of the enzyme is under genetic control. To see if the differences in activity that were observed in vitro between inbred strains of mice were also expressed in vivo, the metabolism of 11-deoxy-[1,2-3H]corticosterone ([1,2-3H]DOC) was studied in BALB/c (C) and C57BL/6 (B6) mice. Maximum radioactivity appeared in most organs within 5-10 min after ip injection. Uptake of tracer into liver was greater for C than B6 mice. Tritium levels in blood, kidney, and pancreas were higher in C mice; levels in adrenal, abdominal fat, and mesentery were higher in B6 mice. In both strains, the concentrations of tracer in tissues, except in gastrointestinal tract, declined and reached a minimum within 60 min. Most of the radioactivity (84%) from [1,2-3H]DOC accumulated in the lumen of the intestinal tract, and few counts were found in the wall. Intestinal concentrations of 3H at different postinjection intervals were greater for B6 than C mice. In contrast, twice as much radioactivity appeared in the kidneys of C than of B6 mice. The organs of excretion (kidney, liver, gall bladder, and intestine) concentrated steroid from blood. Heart, striated muscle, and spleen excluded steroid. Four acidic metabolites of [1,2-3H]DOC were detected in liver, and two were detected in small intestine. Acids formed in liver did not accumulate, and no differences between C and B6 strains were seen. More acid metabolites accumulated in intestines of C mice than in those of B6 mice. The quantitative aspects of steroid acid formation in vivo are consistent with our previous in vitro findings that livers from C mice synthesize more pregnolic acid from DOC than do livers from B6 mice.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1983 by The Endocrine Society