Potential therapeutic role for statins in respiratory disease

被引:151
作者
Hothersall, E.
McSharry, C.
Thomson, N. C. [1 ]
机构
[1] Western Infirm & Associated Hosp, Dept Resp Med, Div Immunol Infect & Inflammat, Glasgow G11 6NT, Lanark, Scotland
[2] Univ Glasgow, Dept Resp Med, Div Immunol Infect & Inflammat, Glasgow G11 6NT, Lanark, Scotland
[3] Univ Glasgow, Dept Immunol, Div Immunol Infect & Inflammat, Glasgow G11 6NT, Lanark, Scotland
关键词
D O I
10.1136/thx.2005.057976
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Statins reduce cholesterol levels by inhibiting 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and have an established role in the treatment of atherosclerotic disease. Recent research has identified anti-inflammatory properties of statins. Statins appear to reduce the stability of lipid raft formation with subsequent effects on immune activation and regulation, and also prevent the prenylation of signalling molecules with subsequent downregulation of gene expression. Both these effects result in reduced cytokine, chemokine, and adhesion molecule expression, with effects on cell apoptosis or proliferation. This review considers the evidence for the anti-inflammatory properties of statins in the lung, and how these effects are being applied to research into the role of statins as a novel treatment of respiratory diseases.
引用
收藏
页码:729 / 734
页数:6
相关论文
共 98 条
[1]  
Aikawa M, 2001, CIRCULATION, V103, P276
[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]   Statins in stroke prevention and carotid atherosclerosis -: Systematic review and up-to-date meta-analysis [J].
Amarenco, P ;
Labreuche, J ;
Lavallée, P ;
Touboul, PJ .
STROKE, 2004, 35 (12) :2902-2909
[4]   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
[5]  
Barnes PJ, 1998, PHARMACOL REV, V50, P515
[6]   HMG-CoA reductase inhibitors reduce MMP-9 secretion by macrophages [J].
Bellosta, S ;
Via, D ;
Canavesi, M ;
Pfister, P ;
Fumagalli, R ;
Paoletti, R ;
Bernini, F .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (11) :1671-1678
[7]   Effects of statins on stroke prevention in patients with and without coronary heart disease: A meta-analysis of randomized controlled trials [J].
Briel, M ;
Studer, M ;
Glass, TR ;
Bucher, HC .
AMERICAN JOURNAL OF MEDICINE, 2004, 117 (08) :596-606
[8]   The cardiac fibroblast: Therapeutic target in myocardial remodeling and failure [J].
Brown, RD ;
Ambler, SK ;
Mitchell, MD ;
Long, CS .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2005, 45 :657-687
[9]   CD40 engagement enhances eosinophil survival through induction of cellular inhibitor of apoptosis protein 2 expression: Possible involvement in allergic inflammation [J].
Bureau, F ;
Seumois, G ;
Jaspar, F ;
Vanderplasschen, A ;
Detry, B ;
Pastoret, PP ;
Louis, R ;
Lekeux, P .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (03) :443-449
[10]  
Carlin CM, 2005, THORAX, V60, pII6