Literature DB >> 3959767

Oxysterols: chemical synthesis, biosynthesis and biological activities.

E J Parish, V B Nanduri, H H Kohl, F R Taylor.   

Abstract

As a class of compounds, oxysterols have demonstrated a wide variety of biological properties. Due to the general interest in these compounds, new methods of chemical synthesis have been developed to provide them for biological investigation. The specific inhibition by oxysterols of cholesterol biosynthesis in mammalian cells has been shown to result primarily from a decrease in cellular levels of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activity. Recent evidence suggests these cellular responses may be mediated by an oxysterol binding protein found in the cytosol of many lines of cultured cells. In certain instances, oxysterols have been shown to be produced in biological systems. These results support the supposition that oxysterols may regulate sterol biosynthesis at the cellular level. Included herein are the inhibitory effects of 9 alpha, 11 alpha-epoxycholest-7-en-3 beta-ol cholest-8-en-3 beta-ol-7-one and cholest-8-en-3 beta-ol-11-one on HMG-CoA reductase activity and their relative affinities for a cytosolic binding protein.

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Year:  1986        PMID: 3959767     DOI: 10.1007/bf02534299

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  33 in total

1.  Inhibitors of cholesterol biosynthesis and the problem of hypercholesterolemia.

Authors:  D S FREDRICKSON; D STEINBERG
Journal:  Ann N Y Acad Sci       Date:  1956-11-16       Impact factor: 5.691

2.  Sterol synthesis. Chemical synthesis of 3beta-benzoyloxy -14alpha, 15alpha-epoxy-5alpha-cholest-7-ene, a key intermediate in the synthesis of 15-oxygenated sterols.

Authors:  E J Parish; T E Spike; G J Schroepfer
Journal:  Chem Phys Lipids       Date:  1977-04       Impact factor: 3.329

3.  Inhibitors of sterol synthesis. Hypocholesterolemic action of dietary 5alpha-cholest-8(14)-en-3beta-ol-15-one in rats and mice.

Authors:  G J Schroepfer; D Monger; A S Taylor; J S Chamberlain; E J Parish; A Kisic; A A Kandutsch
Journal:  Biochem Biophys Res Commun       Date:  1977-10-24       Impact factor: 3.575

4.  Oxygenated sterols as inhibitors of enzymatic conversion of dihydrolanosterol into cholesterol.

Authors:  Y Sato; Y Sonoda; M Morisaki; N Ikekawa
Journal:  Chem Pharm Bull (Tokyo)       Date:  1984-08       Impact factor: 1.645

5.  Different forms of the oxysterol-binding protein. Binding kinetics and stability.

Authors:  A A Kandutsch; F R Taylor; E P Shown
Journal:  J Biol Chem       Date:  1984-10-25       Impact factor: 5.157

6.  Regulation of synthesis and degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase by low density lipoprotein and 25-hydroxycholesterol in UT-1 cells.

Authors:  J R Faust; K L Luskey; D J Chin; J L Goldstein; M S Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

7.  Effect of oxygenated sterols on 3-hydroxy-3-methylglutaryl coenzyme A reductase and DNA synthesis in phytohemagglutinin-stimulated human lymphocytes.

Authors:  M Astruc; M Laporte; C Tabacik; A Crastes de Paulet
Journal:  Biochem Biophys Res Commun       Date:  1978-11-29       Impact factor: 3.575

8.  A novel olefinic rearrangement. The enzymic conversion of cholesta-7,9-dien-3 -ol into cholesta-8,14-dien-3 -ol.

Authors:  M Akhtar; C W Freeman; A D Rahimtula; D C Wilton
Journal:  Biochem J       Date:  1972-09       Impact factor: 3.857

9.  Antagonist action of cholesterol towards the toxicity of hydroxysterols on cultured hepatoma cells.

Authors:  H Hietter; E Trifilieff; L Richert; J P Beck; B Luu; G Ourisson
Journal:  Biochem Biophys Res Commun       Date:  1984-04-30       Impact factor: 3.575

10.  Correlation between oxysterol binding to a cytosolic binding protein and potency in the repression of hydroxymethylglutaryl coenzyme A reductase.

Authors:  F R Taylor; S E Saucier; E P Shown; E J Parish; A A Kandutsch
Journal:  J Biol Chem       Date:  1984-10-25       Impact factor: 5.157

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  6 in total

1.  Syntheses of ring C oxysterols: inhibitors of sterol biosynthesis.

Authors:  Edward J Parish; Chi Luo; Thomas Webb; John D Gorden
Journal:  Lipids       Date:  2007-01-16       Impact factor: 1.880

2.  A facile synthesis and carbon-13 nuclear magnetic resonance spectral properties of 7-ketocholesteryl benzoate.

Authors:  E J Parish; T Y Wei; P Livant
Journal:  Lipids       Date:  1987-10       Impact factor: 1.880

3.  Differential sensitivity of astrocyte primary cultures and derived spontaneous transformed cell lines to 7 beta-hydroxycholesterol: effect on plasma membrane lipid composition and fluidity, and on cell surface protein expression.

Authors:  A Kupferberg; G Cremel; P Behr; A Van Dorsselaer; B Luu; M Mersel
Journal:  Mol Cell Biochem       Date:  1991-02-27       Impact factor: 3.396

Review 4.  Remote functionalization of the steroid side-chain.

Authors:  E J Parish; N Aksara; T L Boos
Journal:  Lipids       Date:  1997-12       Impact factor: 1.880

5.  Apoptosis induced by oxysterols in murine lymphoma cells and in normal thymocytes.

Authors:  M Christ; B Luu; J E Mejia; I Moosbrugger; P Bischoff
Journal:  Immunology       Date:  1993-03       Impact factor: 7.397

Review 6.  Side-chain oxysterol regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity.

Authors:  E J Parish; S C Parish; S Li
Journal:  Lipids       Date:  1995-03       Impact factor: 1.880

  6 in total

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