Advanced glycation end products, oxidative stress and diabetic nephropathy

被引:311
|
作者
Yamagishi, Sho-ichi [1 ]
Matsui, Takanori [1 ]
机构
[1] Kurume Univ, Sch Med, Dept Pathophysiol & Therapeut Diabet Vasc Complic, Kurume, Fukuoka 830, Japan
关键词
diabetic nephropathy; AGEs; RAGE; oxidative stress; renin-angiotensin system; EPITHELIUM-DERIVED FACTOR; ENDOTHELIAL GROWTH-FACTOR; MONOCYTE CHEMOATTRACTANT PROTEIN-1; CONVERTING ENZYME-INHIBITION; NEUTRALIZING RAGE-ANTIBODY; TYPE-1 RECEPTOR BLOCKER; ANGIOTENSIN-II; GENE-EXPRESSION; FACTOR-BETA; MESANGIAL MATRIX;
D O I
10.4161/oxim.3.2.11148
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
About 246 million people worldwide had diabetes in 2007. The global figure of people with diabetes is projected to increase to 370 million in 2030. As the prevalence of diabetes has risen to epidemic proportions worldwide, diabetic nephropathy has become one of the most challenging health problems. Therapeutic options such as strict blood glucose and blood pressure controls are effective for preventing diabetic nephropathy, but are far from satisfactory, and the number of diabetic patients on end-stage renal disease is still increasing. Therefore, a novel therapeutic strategy that could halt the progression of diabetic nephropathy should be developed. There is accumulating evidence that advanced glycation end products (AGEs), senescent macroprotein derivatives formed at an accelerated rate under diabetes, play a role in diabetic nephropathy via oxidative stress generation. In this paper, we review the pathophysiological role of AGEs and their receptor (RAGE)-oxidative stress system in diabetic nephropathy.
引用
收藏
页码:101 / 108
页数:8
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