Advanced glycation endproducts: what is their relevance to diabetic complications?

被引:310
作者
Ahmed, N. [1 ]
Thornalley, P. J. [1 ]
机构
[1] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
关键词
advanced glycation endproducts; diabetic complications; hyperglycaemia; LC-MS/MS; methylglyoxal; pyridoxamine; thiamine;
D O I
10.1111/j.1463-1326.2006.00595.x
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
Glycation is a major cause of spontaneous damage to proteins in physiological systems. This is exacerbated in diabetes as a consequence of the increase in glucose and other saccharides derivatives in plasma and at the sites of vascular complications. Protein damage by the formation of early glycation adducts is limited to lysine side chain and N-terminal amino groups whereas later stage adducts, advanced glycation endproducts (AGEs), modify these and also arginine and cysteine residues. Metabolic dysfunction in vascular cells leads to the increased formation of methylglyoxal which adds disproportionately to the glycation damage in hyperglycaemia. AGE-modified proteins undergo cellular proteolysis leading to the formation and urinary excretion of glycation free adducts. AGEs may potentiate the development of diabetic complications by activation of cell responses by AGE-modified proteins interacting with specific cell surface receptors, activation of cell responses by AGE free adducts, impairment of protein-protein and enzyme-substrate interactions by AGE residue formation, and increasing resistance to proteolysis of extracellular matrix proteins. The formation of AGEs is suppressed by intensive glycaemic control, and may in future be suppressed by thiamine and pyridoxamine supplementation, and several other pharmacological agents. Increasing expression of enzymes of the enzymatic defence against glycation provides a novel and potentially effective future therapeutic strategy to suppress protein glycation.
引用
收藏
页码:233 / 245
页数:13
相关论文
共 116 条
[1]
Abbas ZG, 1997, E AFR MED J, V74, P803
[2]
Profound mishandling of protein glycation degradation products in uremia and dialysis [J].
Agalou, S ;
Ahmed, N ;
Babaei-Jadidi, R ;
Dawnay, A ;
Thornalley, PJ .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (05) :1471-1485
[3]
Chromatographic assay of glycation adducts in human serum albumin glycated in vitro by derivatization with 6-aminoquinolyl-N-hydroxysuccinimidyl-carbamate and intrinsic fluorescence [J].
Ahmed, N ;
Thornalley, PJ .
BIOCHEMICAL JOURNAL, 2002, 364 (01) :15-24
[4]
Peptide mapping identifies hotspot site of modification in human serum albumin by methylglyoxal involved in ligand binding and esterase activity [J].
Ahmed, N ;
Dobler, D ;
Dean, M ;
Thornalley, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (07) :5724-5732
[5]
Ahmed N, 2002, BIOCHEM J, V364, P1
[6]
Methylglyoxal-derived hydroimidazolone advanced glycation end-products of human lens proteins [J].
Ahmed, N ;
Thornalley, PJ ;
Dawczynski, J ;
Franke, S ;
Strobel, J ;
Stein, G ;
Haik, GM .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (12) :5287-5292
[7]
Degradation products of proteins damaged by glycation, oxidation and nitration in clinical type 1 diabetes [J].
Ahmed, N ;
Babaei-Jadidi, R ;
Howell, SK ;
Beisswenger, PJ ;
Thornalley, PJ .
DIABETOLOGIA, 2005, 48 (08) :1590-1603
[8]
Assay of advanced glycation endproducts in selected beverages and food by liquid chromatography with tandem mass spectrometric detection [J].
Ahmed, N ;
Mirshekar-Syahkal, B ;
Kennish, L ;
Karachalias, N ;
Babaei-Jadidi, R ;
Thornalley, PJ .
MOLECULAR NUTRITION & FOOD RESEARCH, 2005, 49 (07) :691-699
[9]
Processing of protein glycation, oxidation and nitrosation adducts in the liver and the effect of cirrhosis [J].
Ahmed, N ;
Thornalley, PJ ;
Lüthen, R ;
Häussinger, D ;
Sebekova, K ;
Schinzel, R ;
Voelker, W ;
Heidland, A .
JOURNAL OF HEPATOLOGY, 2004, 41 (06) :913-919
[10]
[Anonymous], 1999, Clin. Lab