期刊文献+

单核细胞趋化蛋白-1和Ⅳ型胶原在糖尿病肾病大鼠肾组织中的表达 被引量:2

The expression of MCP-1 and Ⅳ-C in renal tissue of diabetic nephropathy rats
下载PDF
导出
摘要 目的观察单核细胞趋化蛋白-1(MCP-1)、Ⅳ型胶原(Ⅳ-C)在链尿佐菌素诱发的糖尿病肾病(DN)大鼠肾组织中的表达;探讨洛汀新、来氟米特、来适可对DN大鼠肾组织中MCP-1、Ⅳ-C表达的影响。方法将大鼠随机分成五组:正常组(C组)、糖尿病肾病组(D组)、糖尿病肾病洛汀新治疗组(DL组)、糖尿病肾病来氟米特治疗组(DF组)和糖尿病肾病来适可治疗组(DK组)。6周后,用免疫组化方法测定各组肾组织中MCP-1、Ⅳ-C的表达。结果MCP-1在DN大鼠肾小球、肾小管中的表达增高。Ⅳ-C在DL组肾小球中的表达与C组比较差异无显著性,在各治疗组与D组肾小管中的表达差异有显著性(P<0.01)。结论 MCP-1、Ⅳ-C在DN大鼠肾组织中表达增高;洛汀新、来氟米特、来适可能下调MCP-1在DN大鼠肾小球、肾小管中的表达;洛汀新可明显下调Ⅳ-C在DN大鼠肾小球中的表达。 Objective To observe the expression of monocyte chemoattractant protein-1 (MCP-1) and collagen Ⅳ (Ⅳ-C) in renal tissue of diabetic nephropathy rats that was induced by streptozotozin (STZ). To investigate the effects of Lotensin、LEF and Lescol for the expression of MCP-1 and Ⅳ-C in renal tissue of diabetic nephropathy rats. Methods The rats were randomly divided into five groups: normal control group(group C),diabetic nephropathy group (group D) .diabetic nephropathy rats treated with Lotensin (group DL),diabetic nephropathy rats treated with LEF (group DF),diabetic nephropathy rats treated with Lescol (group DK). after 6 weeks. The expression of MCP-1 and Ⅳ-C in renal tissue was detected by immunohisto-chemistry. Results There was high expression of MCP-1 and Ⅳ-C in renal tissue of diabetic nephropathy rats. MCP-1 was decreased by Lotensin, LEF and Lescol (P<0. 01) in glomerulus and tubule, Ⅳ-C was same between DL and C group in glomerulus, however there was different between treated groups and D group. Conclusion There was high expression of MCP-1 and Ⅳ-C in renal tissue of diabetic nephropathy rats. This expression could be inhibited by Lotensin、LEF and Lescol.
出处 《贵州医药》 CAS 2004年第1期10-12,共3页 Guizhou Medical Journal
关键词 糖尿病 肾病 大鼠 单核细胞趋化蛋白-1 Ⅳ型胶原 洛汀新 来氟米特 diabetic nephropathy rat MCP-1 IV-C Lotensin LEF Lescol
  • 相关文献

参考文献9

二级参考文献17

共引文献131

同被引文献42

  • 1张郁苒(综述),于青(审校).影响IgA肾病预后因素的研究新进展[J].国际泌尿系统杂志,2007,27(1):96-100. 被引量:3
  • 2Yang J, Dai C, Liu Y. Systemic administration of naked plasmid encoding hepatocyte growth factor ameliorates chronic renal fibrosis in mice [ J ]. Gene Therapy (Basingstoke), 2001, 8 (19) : 1 470 - 1 479. 被引量:1
  • 3Radford MG, Donadio JV, Bergstral E J, et al. Predicting renal outcome in IgA nephropathy [ J ]. J Am Soc Nephrol, 1997, 8 (2) : 199 - 207. 被引量:1
  • 4Pedagogos E, Hewitson TD, Walker RG, et al. Myofibroblasts involvement in chronic transplant rejection [ J ]. Transplantation, 1997, 64 (8) : 1 192 - 1 197. 被引量:1
  • 5Crupp C, Troche I, Klass C, et al. A novel model to study renal myofi-broblasts formation in vitro [ J ]. Kidney lnt, 2001,59 (2) : 543 - 553. 被引量:1
  • 6Yamashita Y, Jeschke MG, Wolf SE. Differential expression of hepatocyte groeth factor in liver, kidney, lung, and spleen following bum in rats[J]. Cytokine, 2000, 12(9): 1 293 -1 298. 被引量:1
  • 7Ueda T, Takeyama Y, Hori Y, et al. Hepatocyte growth factor increases in injured organs and functions as an organotrophic factor in rats with experimental acute pancreatitis[J]. Pancreas, 2000, 20(1): 84 -93. 被引量:1
  • 8Liu Y, Rajur K, Tolbert E,et al. Endogenous hepatoeyte growth factor ameliorates chronic renal jijury by activating matrix degradation path- ways[J]. Kidney Int, 2000, 58(5) :2 028 - 2 043. 被引量:1
  • 9Yang J, Dai C, Liu Y. Hepatocyte growth factor gene therapy and angiotensin II blockade synergistically attenuate renal interstitial fibrosis in mice[J]. J Am Soc Nephrol, 2002, 13(10):2 464 -2 477. 被引量:1
  • 10Yang J, Liu Y. Dissection of key events in tubular epithelial to myofi- broblast transition and its implications in renal interstitial fibrosis[J]. Am J Pathol, 2001, 159(4) : 1 465 - 1 475. 被引量:1

引证文献2

二级引证文献8

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