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二肽基肽酶4抑制剂对糖尿病肾病保护作用的研究进展 被引量:7

Research in the protective effect of dipeptidyl peptidase 4 inhibitors on diabetic nephropathy
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摘要 糖尿病肾病是糖尿病患者常见的微血管并发症之一,也是引起终末期肾病的主要原因。二肽基肽酶4(DPP-4)抑制剂是一种新型降糖药,不仅降低血糖,还对糖尿病肾病有保护作用。DPP-4抑制剂可通过升高内源性胰高血糖素样肽-1(GLP-1)的水平,改善机体高血糖状态,减少白蛋白尿,降低血压,延缓糖尿病肾病的进展,并且还能调节非GLP-1底物的表达,发挥肾脏保护作用。对DPP-4抑制剂的研究,为糖尿病及其并发症的治疗提供了新的方向。 Diabetic nephropathy is one of the common microvascular complications of diabetes, also is the main cause of end-stage renal disease. Dipeptidyl peptidase-4(DPP-4) inhibitors are new drugs for treatment of diabetes,which not only lower blood sugar,but also has protective effect on diabetic nephropathy. Through increasing the endogenous glucagon-like peptide-1(GLP-1) levels,DPP-4 inhibitors improve the body's blood sugar,reduce albuminuria,lower blood pressure and slow the progress of diabetic nephropathy. And DPP-4 inhibitors have renal protective effect independent of GLP-1 through influencing the expression of other DPP-4 substrates. The study of DPP-4 inhibitors offers a new direction for the treatment of diabetes and its complications.
作者 黄涛 秦洁
出处 《中国现代医生》 2016年第6期155-159,共5页 China Modern Doctor
关键词 DPP-4抑制剂 胰高血糖素样肽-1 糖尿病肾病 糖尿病 Dipeptidyl peptidase-4 inhibitors Glucagon-like peptide-1 Diabetic nephropathy Diabetic
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  • 1陈灏珠.实用内科学[M].北京:人民卫生出版社,1988.1100.
  • 2Packham DK, Alves TP, Dwyer JP, et al. Relative incidence ofESRD versus cardiovascular mortality in proteinuric type 2 diabetes and nephropathy: results from the DIAMETRIC (Diabetes Mellitus Treatment for Renal Insufficiency Consortium) database[J]. Am J Kidney Dis, 2012, 59: 75-83.
  • 3Lim AK, Tesch GH. Inflammation in diabetic nephropathy[J]. Mediators lnflamm, 2012, 2012: 146154. doi: 10.1155/2012/ 146154.
  • 4Zelmanovitz T, Gerchman F, Balthazar AP, et al. Diabetic nephropathy[J]. Diabetol Metab Syndr, 2009, h i0. Steinberg D. Atherogenesis in perspective: hypercholesterolemia and inflammation as partners in crime[J]. Nat Med, 2002, 8: 1211-1217.
  • 5Ma KL, Ruan XZ, Powis SH, et al. Sirolimus modifies cholesterol homeostasis in hepatic cells: a potential molecular mechanism for sirolimus associated dyslipidemia[J]. Transplantation, 2007, 84: 1029-1036.
  • 6Ma KL, Ruan XZ, Powis SH, et al. Inflammatory stress exacerbates lipid accumulation in hepatic cells and fatty livers of apolipoprotein E knockout mice[J]. Hepatology, 2008, 48: 770-781.
  • 7Ma KL, Ruan XZ, Powis SH, et al. Anti-atherosclerotic effects of sirolimus on human vascular smooth muscle cells[J]. Am J Physiol Heart Circ Physiol, 2007, 292: H2721-H2728.
  • 8Tuttle KR. Linking Metabolism and Immunology: Diabetic Nephropathy Is an Inflammatory Disease[J]. J Am Soc Nephrol, 2005, 16: 1537-1538.
  • 9Steinberg D. Atherogenesis in perspective: hypercholesterolemia and inflammation as partners in crime[J]. Nat Med, 2002, 8: 1211-1217.
  • 10Ford ES. Body mass index, diabetes, and C- reactive protein among U.S. adults[J]. Diabetes Care, 1999, 22: 1971-1917.

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