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F12511(依氟米贝)对酰基辅酶A胆固醇酰基转移酶的抑制作用:它会成为一种新型抗动脉粥样硬化治疗药物吗?

Inhibition of acyl-CoA cholesterol acyltransferase by F12511 (Eflucimibe): could it be a new antiatherosclerotic therapeutic?

作者信息

López-Farré Antonio José, Sacristán Daniel, Zamorano-León José J, San-Martín Nuria, Macaya Carlos

机构信息

Cardiovascular Research Unit, Cardiovascular Institute, Hospital Clínico San Carlos, Madrid, Spain.

出版信息

Cardiovasc Ther. 2008 Spring;26(1):65-74. doi: 10.1111/j.1527-3466.2007.00030.x.

Abstract

Lipid-lowering strategies, particularly with statins, have been extremely useful in the prevention of cardiovascular disease. However, many patients who receive statin monotherapy do not achieve the desired cardiovascular benefits. Accumulation of cholesteryl esters within macrophages constitutes the hallmark of foam cells during atherogenesis. The action of acyl-coenzyme A (CoA): cholesterol acyltransferase (ACAT) leads to formation of cholesterol esters. There are two different ACAT isoforms: ACAT1 and ACAT2. A considerable interest to develop ACAT inhibitors has been emerging. This review has been focused on the current knowledge about a new ACAT inhibitor, F12511 or eflucimibe, and more particularly on its antiatherosclerotic properties.

摘要

降脂策略,尤其是使用他汀类药物,在预防心血管疾病方面极为有用。然而,许多接受他汀类药物单药治疗的患者并未获得理想的心血管益处。巨噬细胞内胆固醇酯的积累是动脉粥样硬化形成过程中泡沫细胞的标志。酰基辅酶A(CoA):胆固醇酰基转移酶(ACAT)的作用导致胆固醇酯的形成。有两种不同的ACAT同工型:ACAT1和ACAT2。开发ACAT抑制剂的兴趣日益浓厚。本综述聚焦于关于新型ACAT抑制剂F12511或依氟米贝的现有知识,更特别关注其抗动脉粥样硬化特性。

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