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糖尿病大鼠肾脏4-HNE的表达及促红细胞生成素的干预研究

Expression of 4- HNE in the Kidney of Diabetic Rats and the Protective Effect of Erythropoietin
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摘要 目的:观察糖尿病大鼠肾组织中4羟基壬烯醛(4-HNE)的表达,并探讨促红细胞生成素(EPO)的肾脏保护作用机制。方法:链脲佐菌素(STZ)腹腔注射构建糖尿病大鼠模型,随机分为糖尿病组(D组),EPO组(E组),并设正常对照组(C组)。E组给予EPO皮下注射。分别检测各组大鼠24 h尿蛋白量、血尿素氮(BUN)及血肌酐(Scr)。免疫组化及Western-blot观察各组大鼠肾组织4-HNE的表达情况。结果:E组及D组4周、8周及12周肾脏中的4-HNE的表达较C组明显升高,免疫组化染色积分各组差别有统计学意义(P<0.05),E组4-HNE的表达量低于同时间的D组,差别有统计学意义(P<0.05),Western-blot结果与免疫组化结果相符合。结论:糖尿病大鼠肾脏4-HNE升高,EPO可通过抑制脂质过氧化降低4-HNE的表达,从而起到肾脏保护作用。 Objective: To observe the expression of 4- hydroxynonenal( 4- HNE) in the kidney of STZ induced diabetic rats and investigate the protective effect of erythropoietin( EPO). Methods: Rats were randomly divided into control group( group C),diabetic group( group D) and EPO treated group( group E). Rats of group D and group E were given STZ by intraperitoneal injection to establish models of diabetes. EPO was administered to the diabetic rats in group E for 12 weeks. 24- hour urinary protein,BUN and Scr of each group were measured at the 4th,8th and 12 th weeks. The immunohistochemistry and Western- blot were used to detect the expression of 4- HNE in renal tissue. Results: The expression of 4- HNE in group E was significantly lower than group D( P〈0. 05),but was much higher than group C( P〈0. 05). Conclusion: As an indicator of lipid peroxidation,the expression of4- HNE significantly increases in the kidney of STZ induced diabetic rats. EPO may protect the diabetic kidney through inhibiting the level of lipid peroxidation and decreasing the expression of 4- HNE.
出处 《中国中西医结合肾病杂志》 2016年第3期207-210,I0001,I0002,共6页 Chinese Journal of Integrated Traditional and Western Nephrology
基金 青岛市科技局基金资助项目(No.13-1-3-46-nsh) 青岛市医疗卫生优秀人才培养项目(No.青卫科教字[2014]8号)
关键词 糖尿病肾病 氧化应激 脂质过氧化 4 羟基壬烯醛 促红细胞生成素 Diabetic nephropathy Oxidative stress Lipid peroxidation 4-hydroxynonenal Erythropoietin
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参考文献15

  • 1Shoeb M, Ansari NH, Srivastava SK, et al. 4 - hydroxynonenal in the pathogenesis and progression of human diseases. Curr Med Chem,2014,21 (2) :230 - 237.
  • 2王彦江,谢席胜,冯胜刚.氧化应激与糖尿病肾病足细胞损伤的研究进展[J].中国中西医结合肾病杂志,2011,12(7):651-653. 被引量:18
  • 3刘汉兴,章军建,熊丽,刘辉,张磊.氧化应激在慢性缺血性脑白质损伤中的作用[J].中华神经医学杂志,2010,9(3):245-249. 被引量:10
  • 4Yao H, Edirisinghe I, Rajendrasozhan S, et al. Cigarette smoke - mediated inflammatory and oxidative responses are strain - de- pendentin mice. Am J Physiol Lung Cell Mol Physiol, 2008,294 (6) :Ll174 - L1186.
  • 5Aoshiba K, Koinuma M, Yokohori N, et al. Immunohistochemical evaluation of oxidative stress in routine lungs after cigarette smoke exposure. Inhal Toxicol,2003,15 (10) :1029 -1038.
  • 6肖天林,Mohammad hoeb,Naseem .Ansari.4-羟基壬烯醛在糖尿病大鼠白内障中的代谢及发病中的作用[J].中华眼科杂志,2009,45(3):248-253. 被引量:4
  • 7Kirkham PA, Spooner G, Ffoulkes - Jones C, et al. Cigarette smoke triggers macmphage adhesion and activation:role of lipid peroxidation products and scavenger receptor. Free Radic Biol Med ,2003 ,35 (7) :697 - 710.
  • 8Chaudhary P, Sharma R, Sharma A, et al. Mechanisms of 4 - Hy- droxy -2 - nonenal Induced Pro - and Anti - Apoptotic Signa-ling. Biochemistry ,2010,49 ( 29 ) :6263 - 6275.
  • 9Uchida K, Shiraishi M, Naito Y, et al. Activation of stress signa- ling pathways by the end product of lipid peroxidation. J Biol Chem, 1999,274(34) :2234 - 2242.
  • 10Hiroe T, Naoki S, Masayuki M,et al. Chronic treatment with re- combinant human erythropoietin exerts renoprotective effects beyond hematopoiesis in streptozotocin -induced diabetic rat. Eur J Pharmaco1,2009,612 ( 1 - 3 ) : 106 - 114.

二级参考文献74

  • 1Gilbert RE, Cooper ME. The tubulointerstitium in progressive diabetic kidney disease: more than an aftermath of glomerular injury? Kidney Int, 1999, 56: 1627-1637.
  • 2Ziyadeh FN. Significance of tubulointerstitial changes in diabetic renal disease. Kidney Int Suppl, 1996, 54: S10- S13.
  • 3Eddy AA. Molecular basis of renal fibrosis. Pediatr Nephrol, 2000, 15: 290-301.
  • 4Kalluri R, Neilson EG. Epithelial-mesenchymal transition and its implications for fibrosis. J Clin Invest, 2003, 112: 1776-1784.
  • 5Oldfield MD, Bach LA, Forbes JM, et al. Advanced glycation end products cause epithelial- myofibroblast transdifferentiation via the receptor for advanced glycation end products (RAGE). J Clin Invest, 2001, 108: 1853- 1863.
  • 6Zhang C, Meng X, Zhu Z, et al. Role of connective tissue growth factor in renal tubular epithelial-myofibroblast transdifferentiation and extracellular matrix accumulation in vitro. Life Sci, 2004, 75: 367-379.
  • 7Bottinger EP, Bitzer M. TGF-beta signaling in renal disease. J Am Soc Nephrol, 2002, 13: 2600-2610.
  • 8Massague J, Blain SW, Lo RS. TGFbeta signaling in growth control, cancer, and heritable disorders. Cell, 2000, 103: 295-309.
  • 9Li Y, Yang J, Dai C, et al. Role for integrin-linked kinase in mediating tubular epithelial to mesenchymal transition and renal interstitial fibrogenesis. J Clin Invest, 2004, 113: 503- 516.
  • 10Sharpies EJ, Patel N, Brown P, et al. Erythropoietin protects the kidney against the injury and dysfunction caused by ischemia-reperfusion. J Am Soc Nephrol, 2004, 15: 2115-2124.

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