Literature DB >> 8541332

Effect of FR145237, a novel ACAT inhibitor, on atherogenesis in cholesterol-fed and WHHL rabbits. Evidence for a direct effect on the arterial wall.

M Matsuo1, F Ito, A Konto, M Aketa, M Tomoi, K Shimomura.   

Abstract

The hypocholesterolemic and antiatherosclerotic activities of FR145237, a novel acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor, were evaluated in cholesterol-fed and Watanabe heritable hyperlipidemic (WHHL) rabbits. In the first experiment, rabbits were fed a high cholesterol (1% cholesterol) diet for 2 weeks and further fed a high cholesterol diet containing FR145237 for 8 weeks. FR145237 (0.1, 0.32 and 1.0 mg/kg) dose-dependently lowered the plasma total cholestrol levels by 80%, 96% and 97%, respectively. and reduced aortic atherosclerosis by 44%, 90% and 90%, respectively. To clarify a direct effect of FR145237 at the aortic wall, a second experiment was performed. Rabbits were fed a high-cholesterol diet for 8 weeks to establish aortic atherosclerosis and then fed a normal diet with or without FR145237 for 8 weeks. Cholesterol content in the aorta and the liver was significantly reduced in the FR145237 group (10 mg/kg) by 50% and 43%, respectively, though plasma total cholesterol level did not differ from that in the control group. In the WHHL rabbits, FR145237 (10 mg/kg) did not affect plasma cholesterol level but significantly reduced the atherosclerotic lesion in the coronary arteries by 61%. These results suggest that FR145237 potently lowers the plasma cholesterol level in hypercholesterolemia induced by dietary cholesterol but not that by LDL receptor deficiency, and that FR145237 has a direct antiatherosclerotic activity on the arterial wall independent of its hypocholesterolemic activity.

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Year:  1995        PMID: 8541332     DOI: 10.1016/0005-2760(95)00178-6

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


  7 in total

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Authors:  David Akopian; Jheem D Medh
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2.  Direct effect of an acyl-CoA:cholesterol acyltransferase inhibitor, F-1394, on atherosclerosis in apolipoprotein E and low density lipoprotein receptor double knockout mice.

Authors:  T Chiwata; K Aragane; K Fujinami; K Kojima; S Ishibashi; N Yamada; J Kusunoki
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3.  Massive xanthomatosis and altered composition of atherosclerotic lesions in hyperlipidemic mice lacking acyl CoA:cholesterol acyltransferase 1.

Authors:  M Accad; S J Smith; D L Newland; D A Sanan; L E King; M F Linton; S Fazio; R V Farese
Journal:  J Clin Invest       Date:  2000-03       Impact factor: 14.808

Review 4.  Inhibition of acyl coenzyme A-cholesterol acyltransferase: a possible treatment of atherosclerosis?

Authors:  Therese M Heinonen
Journal:  Curr Atheroscler Rep       Date:  2002-01       Impact factor: 5.113

Review 5.  Macrophage cholesterol homeostasis and metabolic diseases: critical role of cholesteryl ester mobilization.

Authors:  Shobha Ghosh
Journal:  Expert Rev Cardiovasc Ther       Date:  2011-03

6.  Increased atherosclerosis in LDL receptor-null mice lacking ACAT1 in macrophages.

Authors:  S Fazio; A S Major; L L Swift; L A Gleaves; M Accad; M F Linton; R V Farese
Journal:  J Clin Invest       Date:  2001-01       Impact factor: 14.808

Review 7.  Macrophage cholesteryl ester mobilization and atherosclerosis.

Authors:  Shobha Ghosh; Bin Zhao; Jinghua Bie; Jingmei Song
Journal:  Vascul Pharmacol       Date:  2009-10-28       Impact factor: 5.773

  7 in total

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