Fructose-mediated non-enzymatic glycation: sweet coupling or bad modification

被引:184
作者
Schalkwijk, CG
Stehouwer, CDA
van Hinsbergh, VWM
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Clin Chem, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Ctr Med, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Med, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Ctr Med, Inst Cardiovasc Res, Amsterdam, Netherlands
[5] TNO, PG, Gaubius Lab, Leiden, Netherlands
关键词
fructose; glycation; advanced glycation endproducts; diabetes; Maillard reaction; polyol pathway;
D O I
10.1002/dmrr.488
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The Maillard reaction is a process in which reducing sugars react spontaneously with amino groups in proteins to advanced glycation endproducts (AGES). Although an elevated level of glucose had been thought to play a primary role in the Maillard reaction, on a molecular basis, glucose is among the least reactive sugars within biological systems. The formation of AGES is now also known to result from the action of various metabolites other than glucose, which are primarily located intracellularly and participate in the non-enzymatic glycation reaction at a much faster rate, such as fructose, trioses and dicarbonyl compounds. In this review, we considered the glycation reaction with particular attention to the potential role of fructose and fructose metabolites. The two sources for fructose are an exogenous supply from the diet and the endogenous formation from glucose through the aldose reductase pathway. Despite its similar toeightfold higher reactivity, the contribution of extracellular glycation by fructose is considerably less than that by glucose, because of the low plasma concentration of fructose (5 mmol/L glucose vs 35 mumol/L fructose). Intracellularly, fructose is elevated in a number of tissues of diabetic patients in which the polyol pathway is active. In the cells of these tissues, the concentrations of fructose and glucose are of the same magnitude. Although direct evidence is not yet available, it is likely that the high reactivity of fructose and its metabolites may substantially contribute to the formation of intracellular AGES and may contribute to alterations of cellular proteins, dysfunction of cells and, subsequently, to vascular complications. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:369 / 382
页数:14
相关论文
共 148 条
[1]
CROSS-LINKING OF PROTEINS BY ALDOSTRIOSE - REACTION OF THE CARBONYL FUNCTION OF THE KETO AMINES GENERATED INSITU WITH AMINO-GROUPS [J].
ACHARYA, AS ;
CHO, YJ ;
MANJULA, BN .
BIOCHEMISTRY, 1988, 27 (12) :4522-4529
[2]
AHMED N, 1992, CLIN CHEM, V38, P1301
[3]
Effects of glucose intolerance on myocardial function and collagen-linked glycation [J].
Avendano, GF ;
Agarwal, RK ;
Bashey, RI ;
Lyons, MM ;
Soni, BJ ;
Jyothirmayi, GN ;
Regan, TJ .
DIABETES, 1999, 48 (07) :1443-1447
[4]
Advanced glycation end products activate endothelium through signal-transduction receptor RAGE - A mechanism for amplification of inflammatory responses [J].
Basta, G ;
Lazzerini, G ;
Massaro, M ;
Simoncini, T ;
Tanganelli, P ;
Fu, CF ;
Kislinger, T ;
Stern, DM ;
Schmidt, AM ;
De Caterina, R .
CIRCULATION, 2002, 105 (07) :816-822
[5]
Role of oxidative stress in diabetic complications - A new perspective on an old paradigm [J].
Baynes, JW ;
Thorpe, SR .
DIABETES, 1999, 48 (01) :1-9
[6]
Glycoxidation and lipoxidation in atherogenesis [J].
Baynes, JW ;
Thorpe, SR .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (12) :1708-1716
[7]
The role of AGEs in aging: causation or correlation [J].
Baynes, JW .
EXPERIMENTAL GERONTOLOGY, 2001, 36 (09) :1527-1537
[8]
Formation pathways for lysine-arginine cross-links derived from hexoses and pentoses by Maillard processes - Unraveling the structure of a pentosidine precursor [J].
Biemel, KM ;
Reihl, O ;
Conrad, J ;
Lederer, MO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :23405-23412
[9]
ADVANCED PROTEIN GLYCOSYLATION IN DIABETES AND AGING [J].
BROWNLEE, M .
ANNUAL REVIEW OF MEDICINE, 1995, 46 :223-234
[10]
Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820