期刊文献+

宁肾颗粒对IgA肾病大鼠肾保护作用及对肾组织PDGF-BB蛋白表达的影响 被引量:1

Influence of Ningshen Granula on the protection effect of rats with IgA nephropathy and the expression of PDGF-BB in renal tissues
原文传递
导出
摘要 目的:研究宁肾颗粒对IgA肾病模型大鼠肾脏的保护作用及对肾组织血小板源生长因子-BB(PDGFBB)蛋白表达的影响,探讨宁肾颗粒治疗IgA肾病的作用机制。方法:将32只大鼠随机分为空白组,模型组,宁肾颗粒低、高剂量(12、24g/kg)组。采用牛血清白蛋白+LPS+CCl4方法建立实验性IgA肾病大鼠模型。造模成功后,每天分早、晚各给药或等体积0.9%氯化钠溶液1次,连续4周。干预后,检测尿液红细胞数、24h尿蛋白定量,观察肾脏病理及免疫病理,用Western blot法检测肾组织PDGF-BB蛋白表达。结果:与空白组比较,模型组大鼠尿红细胞数、24h尿蛋白定量、肾小球系膜区增殖、IgA荧光强度均增加,肾组织PDGF-BB蛋白表达上调(P<0.05,P<0.01)。与模型组比较,宁肾颗粒低、高剂量组大鼠尿红细胞、24h尿蛋白、肾小球IgA荧光强度均有降低(P<0.05,P<0.01),宁肾颗粒高剂量组肾脏系膜区增殖减轻、肾组织PDGF-BB蛋白表达降低(P<0.01)。结论:宁肾颗粒对IgA肾病模型大鼠肾脏具有保护作用,其机制可能与抑制肾脏PDGF-BB蛋白上调有关。 Objective: To research the protection effect of Ningshen Granula on kidney of rats with IgA nephropathy, and the inl uence on the expression of platelet derived growth factor-BB(PDGF-BB), and to investigate the therapeutic mechanism of Ningshen Granula for IgA nephropathy. Methods: Thirty-two rats were randomly divided into control group, model group, Ningshen Granula low-dose(12g/kg) and high-dose groups(24g/kg). The IgA nephropathy rat model was established according to the method of intragastric administration with lipopolysaccharide, bovine serum albumin and carbon tetrachloride. After the models were established, the rats of the four groups were administered in the morning and evening on every day for consecutive 4 weeks. The red blood cell in urine, 24 hours protein quantitative, renal pathology structure and immunopathogenesis were tested. The Western blot was used to test the expression of PDGF-BB. Results: Compared with the control group, the red blood cell in urine, 24 hours protein quantitative, proliferation of glomerular mesangial area and intensity of glomerular IgA immunol uorescence of the rats in the model group increased signii cantly, and the expression of PDGF-BB of renal tissue increased(P〈0.05, P〈0.01). Compared with the model group, the red blood cell in urine, 24 hours protein quantitative and intensity of glomerular IgA immunol uorescence of the rats in Ningshen Granula low-dose and high-dose groups were decreased(P〈0.05, P〈0.01). Compared with the model group, proliferation of glomerular mesangial area and expression of PDGF-BB protein of renal tissue in Ningshen Granula high-dose group were decreased signii cantly(P〈0.01). Conclusion: Ningshen Granula could protect the kidney of IgAN rats, and the mechanism might be related to the inhibition of the up-regulation expression of PDGF-BB in renal.
出处 《中华中医药杂志》 CAS CSCD 北大核心 2014年第7期2331-2333,共3页 China Journal of Traditional Chinese Medicine and Pharmacy
基金 山东省中医药科技发展计划项目(No.2007-124)~~
关键词 宁肾颗粒 IGA肾病 肾保护作用 血小板源生长因子-BB Ningshen Granula IgA nephropathy Kidney protection Platelet derived growth factor-BB
  • 相关文献

参考文献6

  • 1陆慧瑜,张巧玲,蒋小云,陈丽植,莫樱,陈述枚.IgA肾病大鼠模型的建立[J].中国误诊学杂志,2011,11(6):1264-1267. 被引量:43
  • 2Chen A,Sheu L F,Ding S L,et al.Expefimential IgA nephropathy: monomerie IgA protect glomerulus against antigen deposition.Lab Invest,1996,74(2):736-737.
  • 3Coppo R.Pediatric IgA nephropathy:Clinical and therapeutic perspectives.Sem in Nephrol,2008,28(1):18-26.
  • 4赵林,李安源,王志学,齐芳华.宁肾颗粒治疗小儿难治性原发性肾病综合征疗效观察[J].中国中西医结合杂志,2009,29(8):758-760. 被引量:8
  • 5Sano T,Hiki Y,Kokubo T,et IgA1 molecules accumulate and induce inflammatory cell reaction in ratglomeruli.Nephrol Dial Transplant,2002,17(1):50-56.
  • 6Jurgen Floege,Frank Eitner,Charles E Alpers.A new look at platelet-derived growth factor in renal disease.J Am Soe Nephrol,2008,19(1):12-23.

二级参考文献13

  • 1史炯,金晓明.IgA肾病动物模型研究进展[J].国际病理科学与临床杂志,2005,25(6):556-558. 被引量:6
  • 2汤颖,娄探奇,成彩联,彭晖,关伟明.实验性IgA肾病模型的改进[J].中山大学学报(医学科学版),2006,27(2):184-187. 被引量:108
  • 3蒋小云,陈述枚,杨霁云,易著文.33所医院儿童原发性IgA肾病临床和病理表现调查分析[J].中华儿科杂志,2007,45(4):272-278. 被引量:45
  • 4Coppo R. Pediatric lgA nephropathy: Clinical and therapeutic perspectives[J].Sere in Nephrol,2008,28(1):18 -26.
  • 5Rifni A, Small PA Jr, Teague PO,et al. Experimental lgA nephropathy[J].J Exp Med, 1979,150(5):1161-1173.
  • 6Amore A,Roccatello D, Picciouo G.et al. Processing of IgA aggregates in a rat model of chronic liver disease[J]. Clin Immunol Imrnunopathol, 1997,84(2):107 -114.
  • 7Woodroffe AJ,Gormly AA,Clarkson AR,et al. Experimental cir rhosis and deposition of glomerular IgA immune complexes[J]. Contrid Nephrol, 1984,40 : 51-54.
  • 8Allen AC, Topham PS, Harper SJ ,et al. Leucocyte β1,3 galactosyl transferase activity in lgA nephrapathy[J]. Nephrol Dial Transplant. 1997.12(4):701-706.
  • 9Imai H, Nakamoto Y, Asakura K, et al. Spontaneous glomerular IgA depositon in ddY mice:an animal model of lgA nephritis[J].Kidney Ira, 1985,27(5):756-761.
  • 10Miyawaki S, Muso E. Takeuchi E,et al. Selective breeding for high serun, IgA levels from noninbred ddY mice: isolation of a strain with an early onset of glomerular IgA deposition[J].Nephron,1997,76(2):201- 207.

共引文献48

同被引文献6

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部