Receptor for advanced glycation end products and the cardiovascular complications of diabetes and beyond: Lessons from AGEing

被引:14
作者
Yan, Shi Fang [1 ]
Yan, Shi Du [1 ]
Herold, Kevan [1 ]
Ramsamy, Ravichandran [1 ]
Schmidt, Ann Marie [1 ]
机构
[1] Columbia Univ, Med Ctr, New York, NY 10032 USA
关键词
D O I
10.1016/j.ecl.2006.06.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The presence of elevated blood glucose levels characterizes the diabetic state. Hyperglycemia may be caused by a number of underlying factors; however, the consequences of chronically elevated glucose are similar. Both the macrovasculature and microvasculature are exquisitely sensitive to the long-term effects of elevated blood glucose. Cardiovascular disease remains the leading cause of morbidity and mortality in diabetes, regardless of the underlying cause of hyperglycemia. Although other substrates, such as DNA, are susceptible to glycation, this article addresses the impact of nonenzymatic glycation on the proteome. The impact of Advanced Glycation End products (AGEs) on alteration of protein function and signal transduction mechanisms contributes to the pathogenesis of diabetes complications. This suggests that blocking the generation or molecular impact of AGEs may modulate the complications of diabetes.
引用
收藏
页码:511 / +
页数:15
相关论文
共 71 条
[1]   The myeloperoxidase system of human phagocytes generates Nε-(carboxymethyl)lysine on proteins:: a mechanism for producing advances glycation end products at sites of inflammation [J].
Anderson, MM ;
Requena, JR ;
Crowley, JR ;
Thorpe, SR ;
Heinecke, JW .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (01) :103-113
[2]   S100P stimulates cell proliferation and survival via receptor for activated glycation end products (RAGE) [J].
Arumugam, T ;
Simeone, DM ;
Schmidt, AM ;
Logsdon, CD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (07) :5059-5065
[3]   Prevention of incipient diabetic nephropathy by high-dose thiamine and benfotiamine [J].
Babaei-Jadidi, R ;
Karachalias, N ;
Ahmed, N ;
Battah, S ;
Thornalley, PJ .
DIABETES, 2003, 52 (08) :2110-2120
[4]   At least 2 distinct pathways generating reactive oxygen species mediate vascular cell adhesion molecule-1 induction by advanced glycation end products [J].
Basta, G ;
Lazzerini, G ;
Del Turco, S ;
Ratto, GM ;
Schmidt, AM ;
De Caterina, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (07) :1401-1407
[5]   Randomized trial of an inhibitor of formation of advanced glycation end products in diabetic nephropathy [J].
Bolton, WK ;
Cattran, DC ;
Williams, ME ;
Adler, SG ;
Appel, GB ;
Cartwright, K ;
Foiles, PG ;
Freedman, BI ;
Raskin, P ;
Ratner, RE ;
Spinowitz, BS ;
Whittier, FC ;
Wuerth, JP .
AMERICAN JOURNAL OF NEPHROLOGY, 2004, 24 (01) :32-40
[6]   GLYCATION PRODUCTS AND THE PATHOGENESIS OF DIABETIC COMPLICATIONS [J].
BROWNLEE, M .
DIABETES CARE, 1992, 15 (12) :1835-1843
[7]  
Brownlee M, 1996, CURR OPIN ENDOCRINOL, V3, P291, DOI [10.1097/00060793-199608000-00003, DOI 10.1097/00060793-199608000-00003]
[8]   RAGE blockade stabilizes established atherosclerosis in diabetic apolipoprotein E-null mice [J].
Bucciarelli, LG ;
Wendt, T ;
Qu, W ;
Lu, Y ;
Lalla, E ;
Rong, LL ;
Goova, MT ;
Moser, B ;
Kislinger, T ;
Lee, DC ;
Kashyap, Y ;
Stern, DM ;
Schmidt, AM .
CIRCULATION, 2002, 106 (22) :2827-2835
[9]   The pattern recognition receptor (RAGE) is a counterreceptor for leukocyte integrins: A novel pathway for inflammatory cell recruitment [J].
Chavakis, T ;
Bierhaus, A ;
Al-Fakhri, N ;
Schneider, D ;
Witte, S ;
Linn, T ;
Nagashima, M ;
Morser, J ;
Arnold, B ;
Preissner, KT ;
Nawroth, PP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (10) :1507-1515
[10]   Blockade of late stages of autoimmune diabetes by inhibition of the receptor for advanced glycation end products [J].
Chen, YL ;
Yan, SSD ;
Colgan, J ;
Zhang, HP ;
Luban, J ;
Schmidt, AM ;
Stern, D ;
Herold, KC .
JOURNAL OF IMMUNOLOGY, 2004, 173 (02) :1399-1405