Endothelial Toxicity of High Glucose and its by-Products in Diabetic Kidney Disease

被引:51
作者
Dou, Laetitia [1 ]
Jourde-Chiche, Noemie [1 ,2 ,3 ]
机构
[1] Aix Marseille Univ, INSERM, INRA, C2VN,Fac Pharm, 27 Bd Jean Moulin, F-13005 Marseille, France
[2] Hop Conception, AP HM, Ctr Nephrol & Transplantat Renale, 147 Bd Baille, F-13005 Marseille, France
[3] French Renal Endothelial Soc FRENDS, Marseille, France
关键词
AGEs; diabetic kidney disease; endothelial dysfunction; glucose; polyols; GLYCATION END-PRODUCTS; PROTEIN-KINASE-C; OXIDATIVE STRESS; PROGENITOR CELLS; TGF-BETA; GLOMERULAR ENDOTHELIUM; GENE-EXPRESSION; ANGIOTENSIN-II; NADPH OXIDASE; NEPHROPATHY;
D O I
10.3390/toxins11100578
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Alterations of renal endothelial cells play a crucial role in the initiation and progression of diabetic kidney disease. High glucose per se, as well as glucose by-products, induce endothelial dysfunction in both large vessels and the microvasculature. Toxic glucose by-products include advanced glycation end products (AGEs), a group of modified proteins and/or lipids that become glycated after exposure to sugars, and glucose metabolites produced via the polyol pathway. These glucose-related endothelio-toxins notably induce an alteration of the glomerular filtration barrier by increasing the permeability of glomerular endothelial cells, altering endothelial glycocalyx, and finally, inducing endothelial cell apoptosis. The glomerular endothelial dysfunction results in albuminuria. In addition, high glucose and by-products impair the endothelial repair capacities by reducing the number and function of endothelial progenitor cells. In this review, we summarize the mechanisms of renal endothelial toxicity of high glucose/glucose by-products, which encompass changes in synthesis of growth factors like TGF-beta and VEGF, induction of oxidative stress and inflammation, and reduction of NO bioavailability. We finally present potential therapies to reduce endothelial dysfunction in diabetic kidney disease.
引用
收藏
页数:16
相关论文
共 93 条
[11]   High glucose causes upregulation of cyclooxygenase-2 and alters prostanoid profile in human endothelial cells -: Role of protein kinase C and reactive oxygen species [J].
Cosentino, F ;
Eto, M ;
De Paolis, P ;
van der Loo, B ;
Bachschmid, M ;
Ullrich, V ;
Kouroedov, A ;
Gatti, CD ;
Joch, H ;
Volpe, M ;
Lüscher, TF .
CIRCULATION, 2003, 107 (07) :1017-1023
[12]   Advanced glycation end-products: Implications for diabetic and non-diabetic nephropathies [J].
Daroux, M. ;
Prevost, G. ;
Maillard-Lefebvre, H. ;
Gaxatte, C. ;
D'Agati, V. D. ;
Schmidt, A. M. ;
Boulanger, E. .
DIABETES & METABOLISM, 2010, 36 (01) :1-10
[13]  
Diabet Control Complications DCCT Res Grp, 1995, KIDNEY INT, V47, P1703
[14]   Endothelin receptor-A mediates degradation of the glomerular endothelial surface layer via pathologic crosstalk between activated podocytes and glomerular endothelial cells [J].
Ebefors, Kerstin ;
Wiener, Robert J. ;
Yu, Liping ;
Azeloglu, Evren U. ;
Yi, Zhengzi ;
Jia, Fu ;
Zhang, Weijia ;
Baron, Margaret H. ;
He, John C. ;
Haraldsson, Borje ;
Daehn, Ilse .
KIDNEY INTERNATIONAL, 2019, 96 (04) :957-970
[15]   Time Course and Mechanisms of Circulating Progenitor Cell Reduction in the Natural History of Type 2 Diabetes [J].
Fadini, Gian Paolo ;
Boscaro, Elisa ;
de Kreutzenberg, Saula ;
Agostini, Carlo ;
Seeger, Florian ;
Dimmeler, Stefanie ;
Zeiher, Andreas ;
Tiengo, Antonio ;
Avogaro, Angelo .
DIABETES CARE, 2010, 33 (05) :1097-1102
[16]   BAMBI Elimination Enhances Alternative TGF-β Signaling and Glomerular Dysfunction in Diabetic Mice [J].
Fan, Ying ;
Li, Xuezhu ;
Xiao, Wenzhen ;
Fu, Jia ;
Harris, Ray C. ;
Lindenmeyer, Maja ;
Cohen, Clemens D. ;
Guillot, Nicolas ;
Baron, Margaret H. ;
Wang, Niansong ;
Lee, Kyung ;
He, John C. ;
Schlondorff, Detlef ;
Chuang, Peter Y. .
DIABETES, 2015, 64 (06) :2220-2233
[17]   Gene expression profiles of glomerular endothelial cells support their role in the glomerulopathy of diabetic mice [J].
Fu, Jia ;
Wei, Chengguo ;
Zhang, Weijia ;
Schlondorff, Detlef ;
Wu, Jinshan ;
Cai, Minchao ;
He, Wu ;
Baron, Margaret H. ;
Chuang, Peter Y. ;
Liu, Zhihong ;
He, John Cijiang ;
Lee, Kyung .
KIDNEY INTERNATIONAL, 2018, 94 (02) :326-345
[18]   Dapagliflozin attenuates human vascular endothelial cell activation and induces vasorelaxation: A potential mechanism for inhibition of atherogenesis [J].
Gaspari, Tracey ;
Spizzo, Iressa ;
Liu, HongBin ;
Hu, Yunshan ;
Simpson, Richard W. ;
Widdop, Robert E. ;
Dear, Anthony E. .
DIABETES & VASCULAR DISEASE RESEARCH, 2018, 15 (01) :64-73
[19]   Heparanase Is Essential for the Development of Diabetic Nephropathy in Mice [J].
Gil, Natali ;
Goldberg, Rachel ;
Neuman, Tzahi ;
Garsen, Marjolein ;
Zcharia, Eyal ;
Rubinstein, Ariel M. ;
van Kuppevelt, Toin ;
Meirovitz, Amichay ;
Pisano, Claudio ;
Li, Jin-Ping ;
van der Vlag, Johan ;
Vlodavsky, Israel ;
Elkin, Michael .
DIABETES, 2012, 61 (01) :208-216
[20]   The Endothelium in Diabetic Nephropathy [J].
Gilbert, Richard E. .
CURRENT ATHEROSCLEROSIS REPORTS, 2014, 16 (05)