Peptide mimetics of apolipoproteins improve HDL function

被引:21
作者
Navab, Mohamad [1 ]
Anantharamaiah, G. M. [2 ]
Reddy, Srinivasa T. [1 ]
Van Lenten, Brian J. [1 ]
Buga, Georgette M. [1 ]
Fogelman, Alan M. [1 ]
机构
[1] Univ Calif Los Angeles, Div Cardiol, Dept Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Alabama Birmingham, Dept Med, Atherosclerosis Res Unit, Birmingham, AL 35294 USA
关键词
Apo A-I; Atherosclerosis; HDL; Lipoproteins; Oxidized Lipids; LOW-DENSITY-LIPOPROTEIN; DRAMATICALLY REDUCES ATHEROSCLEROSIS; ACTIVATING-FACTOR-ACETYLHYDROLASE; LDL RECEPTOR-NULL; INHIBITS; MICE; D-4F; CHOLESTEROL; MONKEYS; VASODILATION;
D O I
10.1016/j.jacl.2007.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
During the past decade, evidence has accumulated that suggests that the anti-inflammatory properties of high-density lipoprotein (HDL) may be at least as important as the levels of HDL cholesterol. The recent failure of the torcetrapib clinical trails has highlighted the potential differences between HDL-cholesterol levels and HDL function. Agents to improve HDL function, including HDL anti-inflammatory properties, provide a new therapeutic strategy for ameliorating atherosclerosis and other chronic inflammatory conditions related to dyslipidemia. Seeking guidance from the structure of the apolipoproteins of the plasma lipoproteins has allowed the creation of a series of polypeptides that have interesting functionality with therapeutic implications. In animal models of atherosclerosis, peptide mimetics of apolipoproteins have been shown to improve anti-inflammatory properties of HDL, significantly reduce lesions, and improve vascular inflammation and function without necessarily altering HDL-cholesterol levels. Some of these are now entering the clinical arena as interventions in pharmacologic and pharmacodynamic studies. (C) 2007 National Lipid Association. All rights reserved.
引用
收藏
页码:142 / 147
页数:6
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