Attenuation of inflammation and expansive remodeling by Valsartan alone or in combination with Simvastatin in high-risk coronary atherosclerotic plaques

被引:28
作者
Chatzizisis, Yiannis S. [1 ,2 ]
Jonas, Michael [2 ]
Beigel, Roy [2 ]
Coskun, Ahmet U. [3 ]
Baker, Aaron B. [2 ]
Stone, Benjamin V. [2 ]
Maynard, Charles [4 ]
Gerrity, Ross G. [5 ]
Daley, William [6 ]
Edelman, Elazer R. [1 ,2 ]
Feldman, Charles L. [1 ]
Stone, Peter H. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Div Cardiovasc, Sch Med, Boston, MA 02115 USA
[2] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Northeastern Univ, Boston, MA 02115 USA
[4] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA
[5] Med Coll Georgia, Dept Pathol, Augusta, GA 30912 USA
[6] Novartis Pharmaceut Inc, E Hanover, NJ USA
关键词
Atherosclerosis; Angiotensin receptor blocker; Shear stress; Inflammation; Vascular remodeling; ENDOTHELIAL SHEAR-STRESS; ANGIOTENSIN-II TYPE-1; RECEPTOR BLOCKADE; MATRIX METALLOPROTEINASES; NATURAL-HISTORY; VASCULAR INJURY; ARTERY-DISEASE; AT(1) RECEPTOR; LESIONS; ATHEROGENESIS;
D O I
10.1016/j.atherosclerosis.2008.07.032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: We investigated the role of Valsartan (V) alone or in combination with Simvastatin (S) on coronary atherosclerosis and vascular remodeling, and tested the hypothesis that V or V/S attenuate the pro-inflammatory effect of low endothelial shear stress (ESS). Methods: Twenty-four diabetic, hyperlipidemic swine were allocated into Early (n = 12) and Late (n = 12) groups. In each group animals were treated with Placebo (n = 4), V (it = 4) and V/S (n = 4) and followed for 8 weeks in the Early group and 30 weeks in the Late group. Blood pressure, serum cholesterol and glucose were similar across the treatment Subgroups. ESS was Calculated in plaque-free Subsegments of interest (n = 109) in the Late group at week 23. Coronary arteries of this group were harvested at week 30, and the subsegments of interest were identified, and analyzed histopathologically. Results: V alone or with S reduced the severity of inflammation in high-risk plaques. Both regimens attenuated the severity of enzymatic degradation of the arterial wall, reducing the severity of expansive remodeling. V alone or with S attenuated the pro-inflammatory effect of low ESS. Conclusions: V alone or with S exerts a beneficial effect of reducing and stabilizing high-risk plaque characteristics independent of a blood pressure- and lipid-lowering effect. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:387 / 394
页数:8
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