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肾素血管紧张素系统激活在环孢霉素A肾病中的作用
引用本文:张国华,张训,侯凡凡,王力. 肾素血管紧张素系统激活在环孢霉素A肾病中的作用[J]. 中国危重病急救医学, 2003, 15(12): 754-757
作者姓名:张国华  张训  侯凡凡  王力
作者单位:第一军医大学南方医院肾内科,广东,广州,510515
基金项目:广东省自然科学基金资助课题 ( 970 83 1)
摘    要:目的 :探讨肾素血管紧张素系统 (RAS)的激活在环孢霉素 A (Cs A)肾病中的作用。方法 :低盐饮食大鼠皮下注射 Cs A(1 5 mg· kg- 1· d- 1 ) 2 8d制成 Cs A肾病模型。 Cs A肾病大鼠分别胃内灌入自来水、盐酸维拉帕米、依那普利 ,剂量均为 1 0 m g· kg- 1· d- 1。采用放射免疫法检测各组实验动物血管紧张素 (Ang )水平 ;Northern杂交检测肾组织血管紧张素 1型受体 (AT1 R) m RNA的表达 ,同时对各组实验动物肾间质纤维化程度进行半定量计分。结果 :Cs A处理组血浆和肾组织 Ang 水平为 (4 92± 92 ) ng/L 和 (2 9.8± 6 .0 ) ng/g,均明显高于对照组 (1 90± 36 ) ng/L和 (8.7± 1 .7) ng/g,P均 <0 .0 0 1 ;而依那普利可以明显降低血浆和肾组织 Ang 水平 (P均 <0 .0 5 )。 Cs A处理后出现明显的肾间质纤维化 ,依那普利能明显减轻肾间质纤维化 ,盐酸维拉帕米对肾间质纤维化无显著改善。结论 :RAS的激活在 Cs A肾间质纤维化过程中起重要作用 ,阻断 RAS可以明显减轻 Cs A引起的肾间质纤维化。

关 键 词:环孢霉素A 血管紧张素Ⅱ 肾小管间质纤维化
文章编号:1003-0603(2003)12-0754-04
修稿时间:2003-04-20

Role of activation of renin angiotensin system in cyclosporine A nephropathy
ZHANG Guohua,ZHANG Xun,HOU Fanfan,WANG Li. Role of activation of renin angiotensin system in cyclosporine A nephropathy[J]. Chinese critical care medicine, 2003, 15(12): 754-757
Authors:ZHANG Guohua  ZHANG Xun  HOU Fanfan  WANG Li
Affiliation:Department of Nephrology, Nanfang Hospital, The First Military Medical University, Guangzhou 510515, Guangdong, China.
Abstract:OBJECTIVE: To investigate the role of renin angiotensin system (RAS) activation in cyclosporine A nephropathy. METHODS: Rats were fed with low salt diet. After seven days, they were randomly divided into four groups: vehicle (n=7), CsA treated (n=7), CsA+verapamil (n=7), CsA+enalapril (n=7). All rats except vehicle received a daily subcutaneous injection of CsA (15 mg/kg) for four weeks. Plasma and renal tissue angiotensin II (Ang II) levels were measured by radioimmunoassay. The expression of angiotensin II type 1 receptor (AT1R) was examined by Northern blot. RESULTS: Plasma and renal tissue angiotensin II levels were significantly elevated in CsA treated rats when compared to that in vehicle rats ((190+/-36)ng/L vs. (492+/-92)ng/L, (29.8+/-6.0)ng/g vs. (8.7+/-1.7) ng/g, P<0.001). Enalapril reduced angiotensin II levels significantly (both P<0.05). The expression of AT1R mRNA was down-regulated by CsA, this down-regulation was reversed by enalapril. CsA treated animals showed marked tubulointerstitial fibrosis, enalapril lessened the tubulointerstitial fibrosis significantly (P<0.05). Verapamil did not improve tubulointerstitial fibrosis significantly (P>0.05). CONCLUSION: RAS activation plays an important part in CsA nephropathy. Blockade of RAS may retard the progression of tubulointerstitial fibrosis caused by CsA.
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