Literature DB >> 836857

Effects of 25-hydroxycholesterol and 7-ketocholesterol, inhibitors of sterol synthesis, administered orally to mice.

A A Kandutsch, H J Heiniger, H W Chen.   

Abstract

When 25-hydroxycholesterol or 7-ketocholesterol was fed to mice with the diet, growth was suppressed and mature mice lost weight. The effect of the 7-ketone upon body weight was effectively counteracted by cholesterol whereas cholestanol and beta-sitosterol were ineffective. Growth repression due to 25-hydroxycholesterol was only partially relieved by cholesterol. The effects of 25-hydroxycholesterol and 7-ketocholesterol upon body weight were related to an apparent effect upon appetite. However the sterols were not unpalatable since diets containing them were not rejected in favor of control diet. Intestinal sterol synthesis was inhibited soon after the administration of dietary 7-ketocholesterol or 25-hydroxycholesterol but inhibition decreased with prolonged feeding. When fed by gavage, the sterols suppressed intestinal sterol synthesis as soon as 2 h after administration. In contrast, cholesterol administered by gavage did not affect intestinal sterol synthesis during a 24 h test period. When fed with the diet 25-hydroxycholesterol and 7-ketocholesterol did not depress hepatic cholesterol synthesis beyond the low levels found in pair-fed controls. Inhibition of intestinal sterol synthesis was accompanied by a decrease in the concentration of cholesterol in the intestinal mucosa and, usually, by a drop in the molar ratio of cholesterol to phospholipids.

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Year:  1977        PMID: 836857     DOI: 10.1016/0005-2760(77)90022-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  8 in total

1.  Transformation of 25-Hydroxycholesterol by Rhizoctonia muneratii.

Authors:  M E Wozny; T R Smith; R L Angus; E T Kaiser
Journal:  Appl Environ Microbiol       Date:  1982-03       Impact factor: 4.792

2.  A relationship between the activities of hepatic lanosterol 14 alpha-demethylase and 3-hydroxy-3-methylglutaryl-CoA reductase.

Authors:  C Marco de la Calle; W Hwang; C R Pullinger; G F Gibbons
Journal:  Biochem J       Date:  1988-02-15       Impact factor: 3.857

3.  Inhibition of cholesterol synthesis by oxygenated sterols.

Authors:  A A Kandutsch; H W Chen
Journal:  Lipids       Date:  1978-10       Impact factor: 1.880

4.  Knockout of mouse Cyp3a gene enhances synthesis of cholesterol and bile acid in the liver.

Authors:  Mari Hashimoto; Kaoru Kobayashi; Mio Watanabe; Yasuhiro Kazuki; Shoko Takehara; Asumi Inaba; Shin-Ichiro Nitta; Naoto Senda; Mitsuo Oshimura; Kan Chiba
Journal:  J Lipid Res       Date:  2013-05-24       Impact factor: 5.922

5.  Inhibition of hepatic cholesterol synthesis in mice by sterols with shortened and stereochemically varied side chains.

Authors:  K A Erickson; W R Nes
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

6.  Absorption of dietary cholesterol oxidation products and their downstream metabolic effects are reduced by dietary apple polyphenols.

Authors:  Yamato Ogino; Kyoichi Osada; Shingo Nakamura; Yutaka Ohta; Tomomasa Kanda; Michihiro Sugano
Journal:  Lipids       Date:  2007-02-10       Impact factor: 1.880

7.  Binding of 25-hydroxycholesterol and cholesterol to different cytoplasmic proteins.

Authors:  A A Kandutsch; H W Chen; E P Shown
Journal:  Proc Natl Acad Sci U S A       Date:  1977-06       Impact factor: 11.205

8.  Oxidized cholesterol modulates age-related change in lipid metabolism in rats.

Authors:  K Osada; T Kodama; S Noda; K Yamada; M Sugano
Journal:  Lipids       Date:  1995-05       Impact factor: 1.880

  8 in total

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