Robarts Research Institute and Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada, N6A 5K8.
Cardiovasc Ther. 2011 Oct;29(5):327-39. doi: 10.1111/j.1755-5922.2010.00142.x. Epub 2010 Apr 9.
Inhibition of cholesteryl ester transfer protein (CETP), a key protein involved in reverse cholesterol transport, can lead to increases in high-density lipoprotein cholesterol (HDL-C) levels and thus, is under evaluation as an antiatherogenic strategy. Several CETP inhibitors have been under development including anacetrapib, dalcetrapib, and torcetrapib. To date, anacetrapib demonstrates the greatest HDL-C raising and low-density lipoprotein cholesterol (LDL-C) lowering potential. Phase I and phase II trials with anacetrapib have revealed that anacetrapib is well-tolerated and does not seem to possess the pressor effects associated with torcetrapib. This article will briefly review the HDL-C raising through CETP inhibition as an antiatherogenic strategy with a specific focus on anacetrapib.
抑制胆固醇酯转移蛋白(CETP),一种参与胆固醇逆转运的关键蛋白,可导致高密度脂蛋白胆固醇(HDL-C)水平升高,因此,作为一种抗动脉粥样硬化策略正在评估中。目前正在开发几种 CETP 抑制剂,包括依泽替米贝、达塞曲匹和托彻普。迄今为止,依泽替米贝显示出最大的升高高密度脂蛋白胆固醇(HDL-C)和降低低密度脂蛋白胆固醇(LDL-C)的潜力。依泽替米贝的 I 期和 II 期临床试验表明,依泽替米贝耐受性良好,似乎没有与托彻普相关的升压作用。本文将简要回顾通过 CETP 抑制升高 HDL-C 作为一种抗动脉粥样硬化策略,特别关注依泽替米贝。