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Effects of dietary 27-hydroxycholesterol on cholesterol metabolism and bile acid biosynthesis in the hamster

Authors :
Jacqueline Férézou
Carole Loison
Sandrine Dubrac
Maâmar Souidi
Michel Parquet
Michel Riottot
Claude Lutton
Colette Sérougne
Nawel Boudem
Fabien Milliat
Thierry Bécue
Institut de Radioprotection et de Sûreté Nucléaire (IRSN)
Université Paris Sud Orsay
Source :
Canadian Journal of Physiology and Pharmacology, Canadian Journal of Physiology and Pharmacology, 2003, 81 (9), pp.854-863. ⟨10.1139/y03-079⟩
Publication Year :
2003
Publisher :
HAL CCSD, 2003.

Abstract

27-hydroxycholesterol (27OH-Chol) is an important endogenous oxysterol resulting from the action of sterol 27-hydroxylase (CYP27A1) on cholesterol in the liver and numerous extrahepatic tissues. It may act as a modulator of cholesterol and bile acid metabolism. The effects of 27OH-Chol on the main enzymes and receptors of cholesterol metabolism were investigated by feeding male hamsters a diet supplemented with 27OH-Chol (0.1% w/w) for 1 week. Intestinal scavenger class B, type I (SR-BI) protein level was decreased (–65%), but hepatic expression was increased (+34%). Liver 3β-hydroxy-3β-methyl glutaryl coenzyme A reductase (–58%), cholesterol 7α-hydroxylase (–54%), oxysterol 7α-hydroxylase (–44%), and sterol 12α-hydroxylase (–70%) activities were all decreased. Bile acid composition was changed (fourfold increase in the chenodeoxycholic/cholic acid ratio). This study demonstrates that dietary 27OH-Chol modulates major enzymes of cholesterol metabolism and alters the biliary bile acid profile, making it more hydrophobic, at least at this level of intake. Its effects on SR-BI protein levels are organ dependent. The properties of 27OH-Chol or its metabolites on cholesterol metabolism probably result from the activation of specific transcription factors. Key words: cholesterol 7α-hydroxylase (CYP7A1), sterol 12α-hydroxylase (CYP8B1), sterol 27-hydroxylase (CYP27A1), 3β-hydroxy-3β-methyl glutaryl coenzyme A reductase (HMGCoAR), scavenger receptor class B type I (SR-BI).

Details

Language :
English
Database :
OpenAIRE
Journal :
Canadian Journal of Physiology and Pharmacology, Canadian Journal of Physiology and Pharmacology, 2003, 81 (9), pp.854-863. ⟨10.1139/y03-079⟩
Accession number :
edsair.doi.dedup.....077a45ba2685acabc73418b5f13dd525
Full Text :
https://doi.org/10.1139/y03-079⟩