Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†

The oxidation of cholesterol-26-C14, sodium propionate-1, -2, or -3-C14, and sodium octanoate-1-C14 by liver mitochondrial preparations from intact and gonadectomized rats of both sexes, and from intact and gonadectomized rats of both sexes treated with androgens and estrogens, has been studied. Mit...

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Main Authors: David Kritchevsky, Shirley A. Tepper, Ezra Staple, Michael W. Whitehouse
Format: Article
Language:English
Published: Elsevier 1963-04-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520403451
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author David Kritchevsky
Shirley A. Tepper
Ezra Staple
Michael W. Whitehouse
author_facet David Kritchevsky
Shirley A. Tepper
Ezra Staple
Michael W. Whitehouse
author_sort David Kritchevsky
collection DOAJ
description The oxidation of cholesterol-26-C14, sodium propionate-1, -2, or -3-C14, and sodium octanoate-1-C14 by liver mitochondrial preparations from intact and gonadectomized rats of both sexes, and from intact and gonadectomized rats of both sexes treated with androgens and estrogens, has been studied. Mitochondria from intact female rats and mice consistently oxidized added cholesterol to a greater extent than mitochondria from intact males. There were no significant sex differences in the oxidation of sodium propionate (a possible intermediate in the oxidation of the cholesterol side chain to carbon dioxide). Surgical or chemical castration of male rats enhanced cholesterol oxidation. Androgen treatment of female rats slightly depressed cholesterol oxidation but ovariectomy had no effect. Cholesterol oxidation by preparations of normal male or female rat liver mitochondria was inhibited by sex hormones added in vitro. These sex differences in cholesterol oxidation suggest that circulating androgen, rather than estrogen, levels determine the efficiency of cholesterol oxidation. Octanoate oxidation by liver mitochondria was not influenced by prior castration or treatment of male rats with androgens or estrogens. Androgen treatment of female rats slightly inhibited octanoate oxidation while estrogen treatment enhanced octanoate oxidation.
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spelling doaj.art-a64c555de8d84d7baa86e6c724ae3c072022-12-21T21:30:04ZengElsevierJournal of Lipid Research0022-22751963-04-0142188192Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†David Kritchevsky0Shirley A. Tepper1Ezra Staple2Michael W. Whitehouse3The Wistar Institute and Department of Biochemistry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania; Department of Biochemistry, University of Oxford, Oxford, EnglandThe Wistar Institute and Department of Biochemistry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania; Department of Biochemistry, University of Oxford, Oxford, EnglandThe Wistar Institute and Department of Biochemistry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania; Department of Biochemistry, University of Oxford, Oxford, EnglandThe Wistar Institute and Department of Biochemistry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania; Department of Biochemistry, University of Oxford, Oxford, EnglandThe oxidation of cholesterol-26-C14, sodium propionate-1, -2, or -3-C14, and sodium octanoate-1-C14 by liver mitochondrial preparations from intact and gonadectomized rats of both sexes, and from intact and gonadectomized rats of both sexes treated with androgens and estrogens, has been studied. Mitochondria from intact female rats and mice consistently oxidized added cholesterol to a greater extent than mitochondria from intact males. There were no significant sex differences in the oxidation of sodium propionate (a possible intermediate in the oxidation of the cholesterol side chain to carbon dioxide). Surgical or chemical castration of male rats enhanced cholesterol oxidation. Androgen treatment of female rats slightly depressed cholesterol oxidation but ovariectomy had no effect. Cholesterol oxidation by preparations of normal male or female rat liver mitochondria was inhibited by sex hormones added in vitro. These sex differences in cholesterol oxidation suggest that circulating androgen, rather than estrogen, levels determine the efficiency of cholesterol oxidation. Octanoate oxidation by liver mitochondria was not influenced by prior castration or treatment of male rats with androgens or estrogens. Androgen treatment of female rats slightly inhibited octanoate oxidation while estrogen treatment enhanced octanoate oxidation.http://www.sciencedirect.com/science/article/pii/S0022227520403451
spellingShingle David Kritchevsky
Shirley A. Tepper
Ezra Staple
Michael W. Whitehouse
Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
Journal of Lipid Research
title Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
title_full Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
title_fullStr Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
title_full_unstemmed Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
title_short Influence of sex and sex hormones on the oxidation of cholesterol-26-C14 by rat liver mitochondria*†
title_sort influence of sex and sex hormones on the oxidation of cholesterol 26 c14 by rat liver mitochondria †
url http://www.sciencedirect.com/science/article/pii/S0022227520403451
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AT ezrastaple influenceofsexandsexhormonesontheoxidationofcholesterol26c14byratlivermitochondria
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