Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol

Incubation of [4-14C] cholesteryl palmitate with the 12,000 g supernatant fraction of adult rat brain fortified with an NADPH-generating system and β-mercaptoethylamine resulted in formation (2–5%) of more polar metabolites characterized as a mixture of cholesterol-5,6-epoxides. Under extended incub...

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Main Authors: Charles M. Martin, Harold J. Nicholas
Format: Article
Language:English
Published: Elsevier 1973-11-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520368425
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spelling doaj-cc3ad4b5b07e44398722f8c3a33f787e2021-04-24T05:49:23ZengElsevierJournal of Lipid Research0022-22751973-11-01146618624Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triolCharles M. Martin0Harold J. Nicholas1Institute of Medical Education and Research and Department of Biochemistry, St. Louis University School of Medicine, St. Louis, Missouri 63104Institute of Medical Education and Research and Department of Biochemistry, St. Louis University School of Medicine, St. Louis, Missouri 63104Incubation of [4-14C] cholesteryl palmitate with the 12,000 g supernatant fraction of adult rat brain fortified with an NADPH-generating system and β-mercaptoethylamine resulted in formation (2–5%) of more polar metabolites characterized as a mixture of cholesterol-5,6-epoxides. Under extended incubation conditions, cholestane-3β,5α,6β-triol was isolated as the major end product of the incubations. Free [4-14C]cholesterol incubated under similar conditions was not oxidized, whereas oxidation of [4-14C]cholesteryl palmitate appeared to be dependent upon hydrolysis of the ester by the rat brain microsomal subcellular fraction. Elimination of the NADPH-generating system or the addition of EDTA to the incubation mixture inhibited epoxide formation, suggesting that the products are derived from an NADPH-dependent enzymatic lipoperoxidation mechanism. The in vitro conversion of [4-14C] cholesterol-5α,6α-epoxide to cholestane-3β,5α,6β-triol was also demonstrated in rat brain subcellular fractions in the absence of added cofactors.http://www.sciencedirect.com/science/article/pii/S0022227520368425brain cholesterolcholesterol oxidation
collection DOAJ
language English
format Article
sources DOAJ
author Charles M. Martin
Harold J. Nicholas
spellingShingle Charles M. Martin
Harold J. Nicholas
Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
Journal of Lipid Research
brain cholesterol
cholesterol oxidation
author_facet Charles M. Martin
Harold J. Nicholas
author_sort Charles M. Martin
title Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
title_short Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
title_full Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
title_fullStr Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
title_full_unstemmed Metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
title_sort metabolism of cholesteryl palmitate by rat brain in vitro; formation of cholesterol epoxides and cholestane-3β,5α,6β-triol
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1973-11-01
description Incubation of [4-14C] cholesteryl palmitate with the 12,000 g supernatant fraction of adult rat brain fortified with an NADPH-generating system and β-mercaptoethylamine resulted in formation (2–5%) of more polar metabolites characterized as a mixture of cholesterol-5,6-epoxides. Under extended incubation conditions, cholestane-3β,5α,6β-triol was isolated as the major end product of the incubations. Free [4-14C]cholesterol incubated under similar conditions was not oxidized, whereas oxidation of [4-14C]cholesteryl palmitate appeared to be dependent upon hydrolysis of the ester by the rat brain microsomal subcellular fraction. Elimination of the NADPH-generating system or the addition of EDTA to the incubation mixture inhibited epoxide formation, suggesting that the products are derived from an NADPH-dependent enzymatic lipoperoxidation mechanism. The in vitro conversion of [4-14C] cholesterol-5α,6α-epoxide to cholestane-3β,5α,6β-triol was also demonstrated in rat brain subcellular fractions in the absence of added cofactors.
topic brain cholesterol
cholesterol oxidation
url http://www.sciencedirect.com/science/article/pii/S0022227520368425
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AT haroldjnicholas metabolismofcholesterylpalmitatebyratbraininvitroformationofcholesterolepoxidesandcholestane3b5a6btriol
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