西安交通大学学报(医学版)
西安交通大學學報(醫學版)
서안교통대학학보(의학판)
JOURNAL OF XI'AN JIAOTONG UNIVERSITY(MEDICAL SCIENCES)
2010年
1期
110-114
,共5页
任艳芸%孙万森%赵艳龙%马巧亚%王竹
任豔蕓%孫萬森%趙豔龍%馬巧亞%王竹
임염예%손만삼%조염룡%마교아%왕죽
阿霉素肾病%蛋白尿%阴离子位点%祛风通络方
阿黴素腎病%蛋白尿%陰離子位點%祛風通絡方
아매소신병%단백뇨%음리자위점%거풍통락방
adriamycin nephropathy%proteinuria%anionic site%Qufengtongluo Recipe
目的 观察祛风通络方对阿霉素肾病大鼠肾小球基底膜(GBM)上阴离子位点(AS)的影响.方法 尾静脉注射阿霉素建立阿霉素肾病(AN)大鼠模型,并随机分为A(空白组)、B(模型组)、C(祛风通络方组)、D(激素+祛风通络方组)、E(激素组)、F(苯那普利组)组,并给予相应干预;第3、7周留取肾皮质,以醋酸铀和柠檬酸铅双重染色法,透射电镜观察GBM的超微结构;以PEI示踪染色电镜观察GBM上AS的分布变化.结果 ①3周时与A组相比,模型组大鼠24h尿蛋白显著升高(P<0.01),血清ALB明显下降(P<0.01),血清TG和TCH明显升高(P<0.01);②3周时透射电镜示模型组大鼠肾小球足突呈部分或弥漫性融合,GBM上AS明显减少;③7周时与B组相比,C、E组超微结构明显改善,AS分布呈连续点线状分布,平均AS表达量增强(P<0.01).结论 祛风通络方可通过改善GBM上AS的表达与分布而修复肾小球电荷屏障.
目的 觀察祛風通絡方對阿黴素腎病大鼠腎小毬基底膜(GBM)上陰離子位點(AS)的影響.方法 尾靜脈註射阿黴素建立阿黴素腎病(AN)大鼠模型,併隨機分為A(空白組)、B(模型組)、C(祛風通絡方組)、D(激素+祛風通絡方組)、E(激素組)、F(苯那普利組)組,併給予相應榦預;第3、7週留取腎皮質,以醋痠鈾和檸檬痠鉛雙重染色法,透射電鏡觀察GBM的超微結構;以PEI示蹤染色電鏡觀察GBM上AS的分佈變化.結果 ①3週時與A組相比,模型組大鼠24h尿蛋白顯著升高(P<0.01),血清ALB明顯下降(P<0.01),血清TG和TCH明顯升高(P<0.01);②3週時透射電鏡示模型組大鼠腎小毬足突呈部分或瀰漫性融閤,GBM上AS明顯減少;③7週時與B組相比,C、E組超微結構明顯改善,AS分佈呈連續點線狀分佈,平均AS錶達量增彊(P<0.01).結論 祛風通絡方可通過改善GBM上AS的錶達與分佈而脩複腎小毬電荷屏障.
목적 관찰거풍통락방대아매소신병대서신소구기저막(GBM)상음리자위점(AS)적영향.방법 미정맥주사아매소건립아매소신병(AN)대서모형,병수궤분위A(공백조)、B(모형조)、C(거풍통락방조)、D(격소+거풍통락방조)、E(격소조)、F(분나보리조)조,병급여상응간예;제3、7주류취신피질,이작산유화저몽산연쌍중염색법,투사전경관찰GBM적초미결구;이PEI시종염색전경관찰GBM상AS적분포변화.결과 ①3주시여A조상비,모형조대서24h뇨단백현저승고(P<0.01),혈청ALB명현하강(P<0.01),혈청TG화TCH명현승고(P<0.01);②3주시투사전경시모형조대서신소구족돌정부분혹미만성융합,GBM상AS명현감소;③7주시여B조상비,C、E조초미결구명현개선,AS분포정련속점선상분포,평균AS표체량증강(P<0.01).결론 거풍통락방가통과개선GBM상AS적표체여분포이수복신소구전하병장.
Objective To investigate the expression of anionic site in adriamycin-induced nephropathy (AN) rats, and to further explore the effects of Qufengtongluo Recipe on charge barrier in glomerulus in AN rats. Methods Adriamycin nephropathy was induced by a single tail intravenous injection of adriamycin. Totally 80 rats were randomly divided into normal control group and nephropathy model group. Three weeks later, the nephropathy model was established, and 50 AN rats were randomly divided into five groups: nephropathy model group (B, n=10), Qufeng group (C, n=10), prednisone and Qufeng group (D, n=10), prednisone group (E, n=10) and benazepri group (F, n=10), and they were treated respectively. With treatment being given respectively, renal tissue samples in each group were collected at week 3 and 7, respectively. The ultrastructure and expression of anionic site were examined by electron microscope observation. Results ① After adriamycin injection, a significant increase of the 24-hour urinary protein was observed at week 3 (P<0.01). In AN rats, serum albumin was decreased (P<0.01) while serum TCH and TG were increased (P<0.01). ② In AN rats the diffuse fusion and effacement of foot processes and decrease of anionic sites in GBM were observed at week 3. ③ At week 7, the average intensity of AS dramatically increased in C and E groups (P<0.01) compared with that in nephropathy model group. Conclusion The abnormal expression of AS is the important mechanism that leads to the occurrence and development of proteinuria in AN rats. It is possible that Qufengtongluo Recipe has effects on nephrotic syndrome through altering the charge barrier in GBM in glomerulus.