Statins exert differential effects on angiotensin II-induced atherosclerosis, but no benefit for abdominal aortic aneurysms

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Jian-an Wang , Wen-ai Chen , Yifan Wang , Songzhao Zhang , Honghao Bi , Bo Hong , Yueqiu Luo , Alan Daugherty , Xiaojie Xie
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引用次数: 30

Abstract

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.

他汀类药物对血管紧张素ii诱导的动脉粥样硬化有不同的作用,但对腹主动脉瘤没有作用
目的汀类药物可减少动脉粥样硬化,但是否能抑制腹主动脉瘤(AAA)扩张仍存在争议。我们假设他汀类药物(瑞舒伐他汀和阿托伐他汀)可以减轻血管紧张素II (AngII)诱导的动脉粥样硬化和aaa。方法和结果60只apoE−/−雄性小鼠在开始28天的AngII输注(1000 ng/kg/min)之前,通过饮用水给予瑞舒伐他汀(10 mg/kg/day)或阿托伐他汀(20 mg/kg/day)。他汀类药物的使用导致治疗性血清药物浓度。瑞舒伐他汀或阿托伐他汀对血管内皮诱导的肾上直径或面积扩张均无显著影响。然而,阿托伐他汀可显著减少主动脉弓和主动脉根横截面内血管增强的动脉粥样硬化病变区域(P <0.001)。动脉粥样硬化的减弱与血清总胆固醇浓度的降低无关。尽管两种他汀类药物均未改变血清MCP-1和MIF浓度,但阿托伐他汀增加了动脉粥样硬化病变中PPAR-α和-γ mRNA的丰度,降低了NF-κB p50、p65、MCP-1和TNF-α mRNA的丰度。该研究表明,两种他汀类药物均不能抑制血管炎诱导的AAA。相反,阿托伐他汀降低血管炎诱导的动脉粥样硬化,血清炎症标志物无变化,但病变部位的抗炎状态升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Atherosclerosis
Atherosclerosis 医学-外周血管病
CiteScore
9.80
自引率
3.80%
发文量
1269
审稿时长
36 days
期刊介绍: Atherosclerosis has an open access mirror journal Atherosclerosis: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Atherosclerosis brings together, from all sources, papers concerned with investigation on atherosclerosis, its risk factors and clinical manifestations. Atherosclerosis covers basic and translational, clinical and population research approaches to arterial and vascular biology and disease, as well as their risk factors including: disturbances of lipid and lipoprotein metabolism, diabetes and hypertension, thrombosis, and inflammation. The Editors are interested in original or review papers dealing with the pathogenesis, environmental, genetic and epigenetic basis, diagnosis or treatment of atherosclerosis and related diseases as well as their risk factors.
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