Anti-Atherosclerotic Molecules Targeting Oxidative Stress and Inflammation

被引:38
作者
Adameova, A.
Xu, Y. J.
Duhamel, T. A.
Tappia, P. S.
Shan, L.
Dhalla, N. S. [1 ]
机构
[1] St Boniface Gen Hosp, Res Ctr, Inst Cardiovasc Sci, Winnipeg, MB R2H 2A6, Canada
关键词
Atherosclerosis; inflammation; oxidative stress; statins; fibrates; novel anti-atherosclerotic drugs; ESTER TRANSFER PROTEIN; HIGH-DENSITY-LIPOPROTEIN; HMG-COA REDUCTASE; CHOLESTEROL ACYLTRANSFERASE INHIBITOR; ANGIOTENSIN-CONVERTING ENZYME; ACTIVATED-RECEPTOR-GAMMA; CORONARY-HEART-DISEASE; REDOX-SENSITIVE GENES; SMOOTH-MUSCLE-CELLS; ACYL-COA;
D O I
10.2174/138161209789058048
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The accumulation of lipids within arteries remains to be the initial impulse for the pathogenesis of atherosclerosis; however, both inflammation and oxidative stress are considered to play a critical role in this process. Several lipid lowering drugs are used as the first line therapy in atherosclerosis; however, different agents have been found to exhibit beneficial effects which are independent of their lipid lowering activity. Both statins and fibrates have been reported to exert anti-inflammatory and anti-oxidative effects in addition to their anti-atherosclerotic actions. Furthermore, anti-hypertensive, anti-diabetic and anti-platelet drugs, which reduce oxidative stress and inflammation, have been shown to attenuate atherosclerosis. In addition, novel substances such as HDL-related agents, cyclopentenone prostaglandins, lipoprotein-associated phospholipase A(2) inhibitors, 5-lipoxygenase pathway inhibitors, acyl CoA: cholesterol acyltransferase inhibitors, analogues of probucol and lysophosphatidic acid antagonists have been developed for the treatment of atherosclerosis as a consequence of their actions on oxidative stress and inflammation. The present article reviews the involvement of inflammation and oxidative stress in the pathogenesis of atherosclerosis and focuses on the mechanisms of some clinically used as well as potential anti-atherosclerotic substances with anti-inflammatory and anti-oxidative properties.
引用
收藏
页码:3094 / 3107
页数:14
相关论文
共 159 条
[1]   The myocardial infarct size-limiting and antiarrhythmic effects of acyl-CoA:: Cholesterol acyltransferase inhibitor VULM 1457 protect the hearts of diabetic-hypercholesterolaernic rats against ischaemial/reperfusion injury both in vitro and in vivo [J].
Adameova, Adriana ;
Ravingerova, Tána ;
Svec, Pavel ;
Faberova, Viera ;
Kuelova, Magdalena .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 576 (1-3) :114-121
[2]   Effect of statin therapy on C-reactive protein levels - The Pravastatin Inflammation/CRP Evaluation (PRINCE): A randomized trial and cohort study [J].
Albert, MA ;
Danielson, E ;
Rifai, N ;
Ridker, PM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (01) :64-70
[3]   The effect of statin therapy on lipoprotein associated phospholipase A2 levels [J].
Albert, MA ;
Glynn, RJ ;
Wolfert, RL ;
Ridker, PM .
ATHEROSCLEROSIS, 2005, 182 (01) :193-198
[5]   Inhibition of acyl-coenzyme A:cholesterol acyltransferase stimulates cholesterol efflux from macrophages and stimulates farnesoid X receptor in hepatocytes [J].
An, Sojin ;
Jang, Young-Soon ;
Park, Ji-Seon ;
Kwon, Byoung-Mog ;
Paik, Young-Ki ;
Jeong, Tae-Sook .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2008, 40 (04) :407-417
[6]   Induction of lectin-like oxidized LDL receptor by oxidized LDL and lysophosphatidylcholine in cultured endothelial cells [J].
Aoyama, T ;
Fujiwara, H ;
Masaki, T ;
Sawamura, T .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1999, 31 (12) :2101-2114
[7]   Effects of F-1394, an Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor, on ACAT activity in HepG2 cells and on hepatic secretion of lipids in triton WR-1339-induced hyperlipidemic rats:: Possible role of hepatic ACAT in very low density lipoprotein secretion [J].
Aragane, K ;
Kusunoki, J ;
Kitamine, T ;
Yamaura, T ;
Ohnishi, H .
JAPANESE JOURNAL OF PHARMACOLOGY, 1998, 76 (03) :309-312
[8]   Atorvastatin and gemfibrozil metabolites, but not the parent drugs, are potent antioxidants against lipoprotein oxidation [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS .
ATHEROSCLEROSIS, 1998, 138 (02) :271-280
[9]   Pleiotropic actions of peroxisome proliferator-activated receptors in lipid metabolism and atherosclerosis [J].
Barbier, O ;
Torra, IP ;
Duguay, Y ;
Blanquart, C ;
Fruchart, JC ;
Glineur, C ;
Staels, B .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (05) :717-726
[10]   Antiinflammatory properties of HDL [J].
Barter, PJ ;
Nicholls, S ;
Rye, KA ;
Anantharamaiah, GM ;
Navab, M ;
Fogelman, AM .
CIRCULATION RESEARCH, 2004, 95 (08) :764-772