Advanced glycation: How are we progressing to combat this web of sugar anomalies in diabetic nephropathy

被引:14
作者
Forbes, JM [1 ]
Thallas-Bonke, V [1 ]
Cooper, ME [1 ]
Thomas, MC [1 ]
机构
[1] Baker Heart Res Inst, Danielle Alberti Mem Ctr Diabet, Vasc Div, Melbourne, Vic 8008, Australia
关键词
advanced glycation end products; diabetes; diabetic nephropathy; AGE inhibitor; cross-link breaker; CML; pentosidine; rage;
D O I
10.2174/1381612043383151
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Advanced glycation end products (AGEs) in diabetic nephropathy have been extensively researched over the last decade and are now firmly established as major players in this disease. The enigma remains the search for the ideal AGE inhibition therapy, which is a great challenge in the context of the structural diversity inherent to AGE chemistry. Certainly, there is a requirement to standardize measurements of circulating and tissue levels of AGEs and to characterize the pathogenic potential of specific AGE moieties. In order to develop more effective, targeted approaches to combat diabetic nephropathy, the mechanisms of action of selective AGE inhibitors and the inter-relationships of advanced glycation with other pathogenic pathways must be addressed.
引用
收藏
页码:3361 / 3372
页数:12
相关论文
共 142 条
  • [1] Pimagedine: a novel therapy for diabetic nephropathy
    Abdel-Rahman, E
    Bolton, WK
    [J]. EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2002, 11 (04) : 565 - 574
  • [2] ACTON S, 1993, J BIOL CHEM, V268, P3530
  • [3] Prevention of incipient diabetic nephropathy by high-dose thiamine and benfotiamine
    Babaei-Jadidi, R
    Karachalias, N
    Ahmed, N
    Battah, S
    Thornalley, PJ
    [J]. DIABETES, 2003, 52 (08) : 2110 - 2120
  • [4] Altered expression and subcellular localization of diacylglycerol-sensitive protein kinase C isoforms in diabetic rat glomerular cells
    Babazono, T
    Kapor-Drezgic, J
    Dlugosz, JA
    Whiteside, C
    [J]. DIABETES, 1998, 47 (04) : 668 - 676
  • [5] GLYCATION ALTERS COLLAGEN FIBRIL ORGANIZATION
    BAI, PM
    PHUA, K
    HARDT, T
    CERNADAS, M
    BRODSKY, B
    [J]. CONNECTIVE TISSUE RESEARCH, 1992, 28 (1-2) : 1 - 12
  • [6] Role of oxidative stress in diabetic complications - A new perspective on an old paradigm
    Baynes, JW
    Thorpe, SR
    [J]. DIABETES, 1999, 48 (01) : 1 - 9
  • [7] Beisswenger P, 2003, DIABETES METAB, V29, pS95
  • [8] FORMATION OF IMMUNOCHEMICAL ADVANCED GLYCOSYLATION END-PRODUCTS PRECEDES AND CORRELATES WITH EARLY MANIFESTATIONS OF RENAL AND RETINAL DISEASE IN DIABETES
    BEISSWENGER, PJ
    MAKITA, Z
    CURPHEY, TJ
    MOORE, LL
    JEAN, S
    BRINCKJOHNSEN, T
    BUCALA, R
    VLASSARA, H
    [J]. DIABETES, 1995, 44 (07) : 824 - 829
  • [9] Diabetes-associated sustained activation of the transcription factor nuclear factor-κB
    Bierhaus, A
    Schiekofer, S
    Schwaninger, M
    Andrassy, M
    Humpert, PM
    Chen, J
    Hong, M
    Luther, T
    Henle, T
    Klöting, I
    Morcos, M
    Hofmann, M
    Tritschler, H
    Weigle, B
    Kasper, M
    Smith, M
    Perry, G
    Schmidt, AM
    Stern, DM
    Häring, HU
    Schleicher, E
    Nawroth, PP
    [J]. DIABETES, 2001, 50 (12) : 2792 - 2808
  • [10] Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy
    Brenner, BM
    Cooper, ME
    de Zeeuw, D
    Keane, WF
    Mitch, WE
    Parving, HH
    Remuzzi, G
    Snapinn, SM
    Zhang, ZX
    Shahinfar, S
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) : 861 - 869