Effects of statins on 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibition beyond low-density lipoprotein cholesterol

被引:249
作者
Liao, JK
机构
[1] Brigham & Womens Hosp, Vasc Med Res Unit, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1016/j.amjcard.2005.06.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins are potent inhibitors of cholesterol biosynthesis and exert beneficial effects in the primary and secondary prevention of coronary artery disease. However, the overall benefits observed with statins appear to occur much earlier and to be greater than what might be expected from changes in lipid levels alone, suggesting effects beyond cholesterol lowering. Indeed, recent studies indicate that some of the cholesterol-independent or "pleiotropic" effects of statins involve improving endothelial function, enhancing the stability of atherosclerotic plaques, decreasing oxidative stress and inflammation, and inhibiting the thrombogenic response. Many of these pleiotropic effects are mediated by inhibition of isoprenoids, which serve as lipid attachments for intracellular signaling molecules. In particular, inhibition of the small guanosine triphosphate-binding proteins Rho, Ras, and Rac, whose proper membrane localization and function are dependent on isoprenylation, may play an important role in mediating the pleiotropic effects of statins. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:24F / 33F
页数:10
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共 107 条
[1]   Essential role of endothelial nitric oxide synthase for mobilization of stem and progenitor cells [J].
Aicher, A ;
Heeschen, C ;
Mildner-Rihm, C ;
Urbich, C ;
Ihling, C ;
Technau-Ihling, K ;
Zeiher, AM ;
Dimmeler, S .
NATURE MEDICINE, 2003, 9 (11) :1370-1376
[2]  
Aikawa M, 2001, CIRCULATION, V103, P276
[3]   The Pravastatin Inflammation CRP Evaluation (PRINCE): Rationale and design [J].
Albert, MA ;
Staggers, J ;
Chew, P ;
Ridker, PM .
AMERICAN HEART JOURNAL, 2001, 141 (06) :893-898
[4]   Platelet deposition on eroded vessel walls at a stenotic shear rate is inhibited by lipid-lowering treatment with atorvastatin [J].
Alfon, J ;
Royo, T ;
Garcia-Moll, X ;
Badimon, L .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (07) :1812-1817
[5]   THE EFFECT OF CHOLESTEROL-LOWERING AND ANTIOXIDANT THERAPY ON ENDOTHELIUM-DEPENDENT CORONARY VASOMOTION [J].
ANDERSON, TJ ;
MEREDITH, IT ;
YEUNG, AC ;
FREI, B ;
SELWYN, AP ;
GANZ, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (08) :488-493
[6]   Platelet alpha(2)-adrenergic receptors in hypercholesterolemia: Relationship between binding studies and epinephrine-induced platelet aggregation [J].
Baldassarre, D ;
Mores, N ;
Colli, S ;
Pazzucconi, F ;
Sirtori, CR ;
Tremoli, E .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1997, 61 (06) :684-691
[7]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[8]   HMG CoA reductase inhibitors reduce plasminogen activator inhibitor-1 expression by human vascular smooth muscle and endothelial cells [J].
Bourcier, T ;
Libby, P .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (02) :556-562
[9]   Cell cycle progression - New therapeutic target for vascular proliferative disease [J].
Braun-Dullaeus, RC ;
Mann, MJ ;
Dzau, VJ .
CIRCULATION, 1998, 98 (01) :82-89
[10]   Hsp90 and caveolin are key targets for the proangiogenic nitric oxide-mediated effects of statins [J].
Brouet, A ;
Sonveaux, P ;
Dessy, C ;
Moniotte, S ;
Balligand, JL ;
Feron, O .
CIRCULATION RESEARCH, 2001, 89 (10) :866-873