Effect of rosuvastatin on expression of angiotensin Ⅱ receptors in rat aortic endothelium after balloon injury
Effect of rosuvastatin on expression of angiotensin Ⅱ receptors in rat aortic endothelium after balloon injury作者机构:Affiliated Hospital of Qingdao University Medical College ofCardiology Qingdao 266003 China
出 版 物:《South China Journal of Cardiology》 (岭南心血管病杂志(英文版))
年 卷 期:2011年第12卷第1期
页 面:49-55页
学科分类:0710[理学-生物学] 1007[医学-药学(可授医学、理学学位)] 071010[理学-生物化学与分子生物学] 100705[医学-微生物与生化药学] 081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 10[医学]
基 金:supported by Science and Technology Bureau of Qingdao City (Grant No. 02-2-kj-yn-25)
主 题:rosuvastatin balloon injury angiotention Ⅱ receptor
摘 要:Background It's established that Angiotensin Ⅱ and its receptors are involved in intimal hyperplasia after balloon injury and stent restenosis. Recent evidence also suggests that statins have some anti-intimal hyperplasia effects. In this study, the effect of Rosuvastatin on expression of angiotensin Ⅱ receptors in rat aortic endothelium after balloon injury is therefore investigated. Methods All 52 Wistar Kyoto rats were established to aorta injury models by 2F balloon catheter, then were randomly divided into sham operation group, aorta injury group and Rosuvastatin-treatment group. After 14 days, the aortic specimens of the animals were harvested and performed immunohistochemistry and determination of molecular biology. Results The results showed that (i) The 14 days-balloon injury induced obvious intima thickening (P 〈 0.01), however, the phenomenon was reduced by 14 daystreatment with Rosuvastatin (P 〈 0.01). (ii) The expressions of angiotention Ⅱ type Ⅰ (AT1) and type Ⅱ (AT2) receptor mRNA and protein were markedly up-regulated by the balloon injury (P 〈 0.01), after 14 days-treatment with Rosuvastatin, the expression of AT1 receptor mRNA and its protein was decreased (P 〈 0.01), but the expression of AT2 receptor mRNA and its protein was further increased (P 〈 0.05). Conclusion In this study, we observed that the balloon injury induced-intima thickening was reduced by Rosuvastatin in rats, which might be linked with the regulation of expression of angiotensin Ⅱ receptors.