阿托伐他汀
瑞舒伐他汀
医学
血管紧张素II
腹主动脉瘤
内科学
内分泌学
胆固醇
他汀类
腹主动脉
主动脉
药理学
动脉瘤
受体
外科
作者
Jianan Wang,Wen-ai Chen,Yifan Wang,Songzhao Zhang,Honghao Bi,Bo Hong,Yueqiu Luo,Alan Daugherty,Xiaojie Xie
出处
期刊:Atherosclerosis
[Elsevier BV]
日期:2011-03-11
卷期号:217 (1): 90-96
被引量:29
标识
DOI:10.1016/j.atherosclerosis.2011.03.005
摘要
Objective Statins reduce atherosclerosis, but it is controversial whether they suppress abdominal aortic aneurysm (AAA) expansion. We hypothesized that statins (rosuvastatin and atorvastatin) would attenuate angiotensin II (AngII)-induced atherosclerosis and AAA. Methods and results Sixty apoE−/− male mice fed a normal diet were administered with either rosuvastatin (10 mg/kg/day) or atorvastatin (20 mg/kg/day) through drinking water for 1 week prior to initiating 28-day AngII infusion (1000 ng/kg/min). Statins administration led to therapeutic serum concentrations of drugs. Administration of either rosuvastatin or atorvastatin exerted no significant effect on AngII-induced expansion of suprarenal diameter or area. However, atorvastatin significantly reduced AngII-augmented atherosclerotic lesion areas in intimas of both aortic arches and cross-sections of aortic roots (P < 0.001). Atherosclerosis was attenuated independent of reductions in serum total cholesterol concentrations. Although serum MCP-1 and MIF concentrations were not changed by either statins, atorvastatin administration increased PPAR-α and -γ mRNA abundances and decreased NF-κB p50, p65, MCP-1 and TNF-α mRNA abundances in atherosclerotic lesions. Conclusions This study demonstrated both statins failed to suppress AngII-induced AAA. In contrast, atorvastatin reduced AngII-induced atherosclerosis associated with no change in serum inflammatory markers but a shift to upregulation of anti-inflammatory status in lesions.
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