Pyripyropene A, an Acyl–Coenzyme A:Cholesterol Acyltransferase 2–Selective Inhibitor, Attenuates Hypercholesterolemia and Atherosclerosis in Murine Models of Hyperlipidemia
Author(s) -
Taichi Ohshiro,
Daisuke Matsuda,
K Sakai,
Chiara Degirolamo,
Hiroaki Yagyu,
Lawrence L. Rudel,
Satoshi Ōmura,
Shun Ishibashi,
Hiroshi Tomoda
Publication year - 2011
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.111.223552
Subject(s) - sterol o acyltransferase , very low density lipoprotein , chemistry , cholesterol , cholesteryl ester , in vivo , hyperlipidemia , intermediate density lipoprotein , acyl coa , apolipoprotein b , lipoprotein , endocrinology , medicine , biochemistry , biology , enzyme , diabetes mellitus , microbiology and biotechnology
Pyripyropene A (PPPA) of fungal origin is the first compound that has been found to strongly and selectively inhibit acyl-coenzyme A:cholesterol acyltransferase 2 (ACAT2) isozyme activity in vitro. The purpose of the present study was to investigate in vivo efficacy of the ACAT2-selective inhibitor in atherosclerosis.
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