Jian-an Wang , Wen-ai Chen , Yifan Wang , Songzhao Zhang , Honghao Bi , Bo Hong , Yueqiu Luo , Alan Daugherty , Xiaojie Xie
{"title":"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","authors":"Jian-an Wang , Wen-ai Chen , Yifan Wang , Songzhao Zhang , Honghao Bi , Bo Hong , Yueqiu Luo , Alan Daugherty , Xiaojie Xie","doi":"10.1016/j.atherosclerosis.2011.03.005","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>Statins reduce atherosclerosis<span><span>, but it is controversial whether they suppress abdominal aortic aneurysm (AAA) expansion. We hypothesized that statins (rosuvastatin and atorvastatin) would attenuate </span>angiotensin II (AngII)-induced atherosclerosis and AAA.</span></p></div><div><h3>Methods and results</h3><p><span>Sixty apoE−/− male mice fed a normal diet were administered with either rosuvastatin (10</span> <span>mg/kg/day) or atorvastatin (20</span> <!-->mg/kg/day) through drinking water for 1 week prior to initiating 28-day AngII infusion (1000<!--> <span>ng/kg/min). Statins administration led to therapeutic serum concentrations of drugs<span><span>. 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 </span>aortic roots (</span></span><em>P</em> <!--><<!--> <span>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.</span></p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":8623,"journal":{"name":"Atherosclerosis","volume":"217 1","pages":"Pages 90-96"},"PeriodicalIF":4.9000,"publicationDate":"2011-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.atherosclerosis.2011.03.005","citationCount":"30","resultStr":"{\"title\":\"Statins exert differential effects on angiotensin II-induced atherosclerosis, but no benefit for abdominal aortic aneurysms\",\"authors\":\"Jian-an Wang , Wen-ai Chen , Yifan Wang , Songzhao Zhang , Honghao Bi , Bo Hong , Yueqiu Luo , Alan Daugherty , Xiaojie Xie\",\"doi\":\"10.1016/j.atherosclerosis.2011.03.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>Statins reduce atherosclerosis<span><span>, but it is controversial whether they suppress abdominal aortic aneurysm (AAA) expansion. We hypothesized that statins (rosuvastatin and atorvastatin) would attenuate </span>angiotensin II (AngII)-induced atherosclerosis and AAA.</span></p></div><div><h3>Methods and results</h3><p><span>Sixty apoE−/− male mice fed a normal diet were administered with either rosuvastatin (10</span> <span>mg/kg/day) or atorvastatin (20</span> <!-->mg/kg/day) through drinking water for 1 week prior to initiating 28-day AngII infusion (1000<!--> <span>ng/kg/min). Statins administration led to therapeutic serum concentrations of drugs<span><span>. 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 </span>aortic roots (</span></span><em>P</em> <!--><<!--> <span>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.</span></p></div><div><h3>Conclusions</h3><p>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.</p></div>\",\"PeriodicalId\":8623,\"journal\":{\"name\":\"Atherosclerosis\",\"volume\":\"217 1\",\"pages\":\"Pages 90-96\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2011-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.atherosclerosis.2011.03.005\",\"citationCount\":\"30\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atherosclerosis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0021915011002619\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atherosclerosis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021915011002619","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
Statins exert differential effects on angiotensin II-induced atherosclerosis, but no benefit for abdominal aortic aneurysms
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 (10mg/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.
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.