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作 者:王小丹[1] 郑秋甫[1] 余霞君[1] 刘胜[1] 曾强[1]
机构地区:[1]解放军总医院,北京100853
出 处:《解放军医学杂志》2000年第3期195-197,共3页Medical Journal of Chinese People's Liberation Army
摘 要:为与血管紧张素转换酶抑制剂(ACEI)苯那普利比较,研究新一代降压药血管紧张素Ⅱ受体拮抗剂芦沙坦对自发性高血压大鼠(SHR)肾功能的影响,以及两药减轻 SHR肾损害可能的机制,设立苯那普利治疗组、芦沙坦治疗组、未治疗组及正常血压对照组,治疗3个月后,检测肾功能、肾组织病理改变,血浆及肾组织内皮素(ET)水平和肾组织中碱性成纤维细胞生长因子(bFGF)的表达。结果显示,芦沙坦降压、延缓SHR尿白蛋白排泄率与苯那普利比较差异无显著性意义,两治疗组肾组织病理损害轻,芦沙坦组血浆、肾组织中ET及苯那普利组肾组织中ET均明显降低,两组肾组织中bFGF的表达均减弱。结果表明,芦沙坦能延缓SHR肾损害,苯那普利和芦沙坦减轻SHR肾损害与其降低ET、抑制bFGF表达可能有关。Compared with ACEI Benazepril, we investigated the effect of angiotension Ⅱ antagonist Losartan on the renal damage in SHR and the protective mechanism of ACEI Benazepril as well as angiotension Ⅱ antago- nist Losartan. SHR at 13 months of age were divided randomly into control group(n = 12), benazepril treated group(n=12 ) and losartan treated group (n = 12 ). Three months after treatment, renal function, pathological changes, ET level in plasma and kidney as well as bFGF expression in renal tissue were measured. After treatment for three months, the BP and UAE in Benazepril and Lorsatan groups reduced significantly and pathological chan- ges in these two groups were milder as well, with no significant difference in potency. Renal ET in Benazepril and ET in plasma and renal tissue in Losartan dereased significantly. bFGF expression in kidney in both groups was reduced. Conclusion: Both Benazepril and Losartan was able to decrease the renal lesion in SHR. It is suggested that the protective effect of Benazepril and Losartan on renal damage might be associated with the reduction of ET and inhibition of bFGF expression.
关 键 词:自发性高血压 肾功能 BFGF ET 苯那普利 芦沙坦
分 类 号:R544.106[医药卫生—心血管疾病] R692[医药卫生—内科学]
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