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氧化应激在血糖波动加速GK大鼠糖尿病肾病发病过程中的作用 被引量:14

Role of oxidative stress in the process of blood glucose fluctuation accelerating the development of diabetic nephropathy in GK rats
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摘要 目的评价氧化应激(OS)在血糖波动加速DN发病过程中的作用。方法 16只雄性GK大鼠随机分为持续高血糖(MS)组与血糖波动(MF)组,另选择8只雄性Wistar大鼠作为正常对照(NC)组。MF组每日错时腹腔注射葡萄糖及皮下注射胰岛素造成血糖波动模型,MS组每日错时腹腔注射葡萄糖造成持续高血糖模型,NC组每日错时腹腔注射等剂量生理盐水,连续6周。每日观察大鼠的一般体征,第6周末检测全日9个时间点的血糖。麻醉处死大鼠,心脏采血,检测血肌酐(Scr)、血尿酸(SUA)、TC、TG等指标的含量;取双侧肾脏,称重,计算肾脏指数;检测肾组织与肾组织线粒体中OS水平,包括丙二醛(MDA)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)的含量;HE染色,光镜下观察大鼠肾脏病理变化。结果与NC组相比,MS组与MF组体重增长速度减慢,肾脏指数、Scr、SUA、TC、TG、肾组织与肾组织线粒体中MDA升高(P<0.05或P<0.01),肾组织与肾组织线粒体中SOD与GSH-Px降低(P<0.05或P<0.01),肾脏病理改变严重;与MS组相比,MF组肾脏指数、Scr、SUA、TC、肾组织与肾组织线粒体中MDA、SOD、GSH-Px等指标及肾脏病理上的变化更明显(P<0.05或P<0.01)。结论 OS水平在糖尿病大鼠肾组织与肾组织线粒体中增强,其在血糖波动加速DN发病过程中发挥重要作用。 Objective To evaluate the role of oxidative stress(OS)in the process of blood glucose fluctuation accelerating the development of diabetic nephropathy in GK rats. Methods A total of 16 male GK rats were selected and divided into two groups:sustained high blood glucose group(MS group)and blood glucose fluctuation group(MF group).Another 8 male Wistar rats were selected as normal control group(NC group).GK rats in MF group were intraperitoneally injected with glucose and subcutaneously injected with insulin at different time points every day for 6weeks.GK rats in MS group were intraperitoneally injected with glucose at different time points every day for 6 weeks.Rats in NC group were injected intraperitoneally with isodose physiological saline at different time points every day for6 weeks.General physical signs of rats were observed daily,and blood glucose at nine time points of the last day of week 6 was tested.Rats were executed after anesthesia.Contents of serum creatinine(Scr),serum uric acid(SUA),TC and TG were detected in the blood drawn from heart;renal index was calculated after both kidneys were weighed;levels of oxidative stress in kidney and renal mitochondria were detected including contents of malondialdehyde(MDA),superoxide dismutase(SOD)and glutathione peroxidase(GSH-Px);the kidney was observed under light microscope for pathological change after HE staining. Results Compared with NC group,weight growth were significantly slowed in MS and MF group;renal index,Scr,SUA,TC,TG and MDA in kidney and renal mitochondria increased significantly(P〈0.05 or P〈0.01),and SOD and GSH-Px in kidney and renal mitochondria decreased significantly(P〈0.05 or P〈0.01),and renal pathological change was more serious.Compared with MS group,renal index,Scr,SUA,TC and MDA,SOD and GSH-Px in kidney and renal mitochondria,as well as renal pathology changed more obviously in MF group(P〈0.05 or P〈0.01). Conclusion Oxidative stress in diabetic rats kidney and renal mitochondria were significantly enhanced,suggesting oxidative stress playing an important role in the process of blood glucose fluctuation accelerating the development of diabetic nephropathy.
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2015年第12期1106-1110,共5页 Chinese Journal of Diabetes
基金 国家自然科学基金(81403373) 浙江省自然科学基金(Y2110738) 浙江省医药卫生科技计划项目(2013KYA221) 浙江省教育厅研究项目(Y201226284)
关键词 GK大鼠 血糖波动 氧化应激 糖尿病肾病 GK rat Blood glucose fluctuation Oxidative stress(OS) Diabetes nephropathy(DN)
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参考文献12

  • 1陆再英,钟南山.内科学.7版,北京:人民卫生出版社.2010:112-113.
  • 2Ceriello A, Esposito K, Piconi L, et al. Oscillating glucose is more deleterious to endothelial function and oxidative stress than mean glucose in normal and type 2 diabetic patients. Dia- betes, 2008,57 : 1349-1354.
  • 3Ceriello A,Motz E. Is sxidative stress the pathogenic mecha- nism underlying insulin resistance, diabetes, and cardiovascular disease? The common soil hypothesis revisited. Arterioscler thromb Vase Biol, 2004,5 : 816-823.
  • 4Evans JL,Goldfine ID, Maddux BA, et al. Are oxidative stress- activated signaling pathways mediators of insulin resistance and: - cell dysfunction? . Diabetes, 2003,52 : 1-8.
  • 5Brownlce M. The pathobiology ofdibaetic complications:auni- lying mechanism. Diabetes, 2005,54 : 1615-1625.
  • 6Cox DJ, Kovatchev BP, Gonder-Frederick L, et al. Relation- ships between hypergl-ycemia and cognitive performance among adults with type 1 and type 2 diabetes. Diabetes Care, 2005, 28:71-79.
  • 7Yanjun W,Yue X,Shixing L. Effect of blood glucose fluctua- tion on the function of rat pancreatic islets in vivo. Regul Pept, 2011,10:6.
  • 8Kim MK,Jung HS,Yoon CS, et al. The effect of glucose fluc- tuation on apoptosis and function of Ins-1 pancreatic beta cells. Korean Diabetes, 2010,34 : 47-54.
  • 9Nishikawa T, Asba T,Kiirtoshi S, et al. Evlauation of urinary 8-hydorxydoexy-guanosine as a novel biomarker of macorva- seulra complication type 2 diabetes. Diabetes Care, 2003,26: 1507-1512.
  • 10Bouderba S,Sanz MN,Sdnchez-Martin C, et al. Hepatic mito- chondrial alterations and increased oxidative stressin nutritional diabetes-prone Psammomys obesus model. Exp Diabetes Res, 2012,2012 : 430176.

二级参考文献13

  • 1Ha H,Lee HB.Reactive oxygen species amplify glucose signalling in renal cells cultured under high glucose and in diabetic kidney.Nephrology (Carlton),2005,10(Suppl):7.
  • 2Brownlee M.The Pathobiology of Diabetic Complications:A Unifying Mechanism.Diabetes,2005,54(6):1615.
  • 3Brookes PS.Mitochondrial nitric oxide synthase.Mitochondrion,2004,3(4):187.
  • 4Haynes V,Elfering S,Traaseth N,et al.Mitochondrial nitric-oxide synthase:enzyme expression,characterization,and regulation.J Bioenerg Biomembr,2004,36(4):341.
  • 5Pacher P,Obrosova IG,Mabley JG,et al.Role of nitrosative stress and peroxynitrite in the pathogenesis of diabetic complications.Emerging new therapeutical strategies.Curr Med Chem,2005,12(3):267.
  • 6Pacher P,Szabo C.Role of peroxynitrite in the pathogenesis of cardiovascular complications of diabetes.Curr Opin Pharmacol,2006,6(2):136.
  • 7Shen X,Zheng S,Thongboonkerd V,et al.Cardiac mitochondrial damage and biogenesis in a chronic model of type 1 diabetes.Am J Physiol Endocrinol Metab,2004,287(5):896.
  • 8Duchen MR.Roles of mitochondria in health and disease.Diabetes,2004,53(Suppl 1):96.
  • 9Yu T,Robotham JL,Yoon Y.Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology.Proc Natl Acad Sci USA,2006,103(8):2653.
  • 10Vanhorebeek I,De Vos R,Mesotten D,et al.Protection of hepatocyte mitochondrial ultrastructure and function by strict blood glucose control with insulin in critically ill patients.Lancet,2005,365(9453):53.

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