Acta Med. 2006, 49: 35-39
https://doi.org/10.14712/18059694.2017.107
Glycation and Advanced Glycation End-Products in Laboratory Experiments in Vivo and in Vitro
References
1. PJ, Moore LL, Brinck-Johnsen T, Curphey TJ. Increased collagenlinked pentosidine and advanced glycosylation end-products in early diabetic nephropathy. J Clin Invest 1993; 92: 212–7.
<https://doi.org/10.1172/JCI116552>
<PubMed>
2. M, Dršata J, Palička V. Inhibitory effect of glycation on catalytic activity of alanine aminotransferase. Mol Cell Biochem 2001; 218: 35–9.
<https://doi.org/10.1023/A:1007280913732>
3. R, Harding JJ. Prevention of cataract in diabetic rats by aspirin, paracetamol (acetaminophen) and ibuprofen. Exp Eye Res 1992; 54: 509–18.
4. D, Yappert MC, Rubini RG, Peterson CA. Distribution of phospholipid- malondialdehyde – adduct in the human lens. Curr Eye Res 1989; 8: 939–46.
<https://doi.org/10.3109/02713688908997397>
5. M, Vlassara H, Cerami A. Inhibition of heparin-catalyzed human antithrombin III activity by nonenzymatic glycation. Diabetes 1984; 33: 532–5.
6. HF, Gabbay KH, Gallop PM. The glycosylation of hemoglobin: relevance to diabetes mellitus. Science 1978; 200: 21–7.
<https://doi.org/10.1126/science.635569>
7. MP, Urdanivia E, Surma M, Wu VY. Increased glycosylation of glomerular basement membrane collagen in diabetes. Biochem Biophys Res Commun 1980; 95: 765–9.
<https://doi.org/10.1016/0006-291X(80)90852-9>
8. C, Talussot C, Ponsin G, Berthezene F. Non enzymatic glycation of apolipoprotein A-I effects on its self-association and lipid binding properties. Biochem Biophys Res Commun 1988; 153: 1060–7.
<https://doi.org/10.1016/S0006-291X(88)81336-6>
9. J. Oxygen transport impairment in diabetes. Diabetes 1976; 25: 832–8.
10. R, Lechner B, Gerbitz KD. Possible significance of advanced glycation end products in serum in end-stage renal disease and in late complications of diabetes. Eur J Clin Chem Clin Biochem 1996; 34: 355–61.
11. J, Beránek M, Palička V. Inhibition of aspartate aminotransferase by glycation in vitro under various conditions. J Enzyme Inhib Med Chem 2002; 17: 31–6.
<https://doi.org/10.1080/14756360290029501>
12. F, Hiller R, Taylor HR. Senile lens changes and diabetes in two population studies. Am J Ophthalmol 1981; 91: 381–95.
<https://doi.org/10.1016/0002-9394(81)90293-2>
13. M, Binder BR. Nonenzymatic glucosylation as a contributing factor to defective fibrinolysis in diabetes mellitus. Haemostasis 1986; 16: 439–46.
14. I, Edelstein D, Brownlee M. Nonenzymatic glycosylation in vitro and in bovine endothelial cells alters basic fibroblast growth factor activity. J Clin Invest 1994; 94: 110–7.
<https://doi.org/10.1172/JCI117296>
<PubMed>
15. RR, Schnider SL. Glucosylation of human collagen. Diabetes 1982; 31: 47–51.
<https://doi.org/10.2337/diab.31.3.S47>
16. S, Lober M, Thiele M, Teuscher E. Properties of i vitro nonenzymatically glycated plasma fibrinogens. Exp Clin Endocrinol 1987; 90: 37–45.
<https://doi.org/10.1055/s-0029-1210670>
17. DE, Atalay M, Niskanen L, Uusitupa M, Hanninen O, Sen CK. Increased resting and exercise-induced oxidative stress in young IDDM men. Diabetes Care 1996; 19: 569–74.
<https://doi.org/10.2337/diacare.19.6.569>
18. JN, Chylack LT. Spectroscopic study on the effects of nonenzymatic glycation in human α-crystallin. Invest Ophthalmol Vis Sci 1987; 28: 790–4.
19. DE, Brooks SM. Erythrocyte spectrin glucosylation in diabetes. Diabetes 1982; 31: 64–9.
<https://doi.org/10.2337/diab.31.3.S64>
20. VM, Vishwanath V, Frank KE, Elmets CA, Dauchot P, Kohn RR. Relation between complications of type I diabetes mellitus and collagen-linked fluorescence. N Engl J Med 1986; 314: 403–8.
<https://doi.org/10.1056/NEJM198602133140702>
21. A, Romsa GJ, Thibert RJ, Cheung RMC, Draisey TF, Mutus B. Glycated calmodulin from platelets as an index of glycemic control. Clin Chem 1993; 39: 815–9.
22. P, Fogarty J, Sell DR, Monnier VM. Chromatographic quantification of plasma and erythrocyty pentosidine in diabetic and uremic subjects. Diabetes 1992; 41: 153–9.
<https://doi.org/10.2337/diab.41.2.153>
23. M, Cimino A, Pagani F, Girelli A. Nonenzymatic glycation of apolipoprotein B in patients with insulin- and noninsulin-dependent diabetes mellitus. Clin Biochem 1995; 28: 587–592.
<https://doi.org/10.1016/0009-9120(95)00041-5>
24. M, Ortweth BJ. Determination of glycation crosslinking by the sugar-dependent incorporation of (14C) lysine into protein. Anal Biochem 1994; 216: 305–12.
<https://doi.org/10.1006/abio.1994.1046>
25. M, Smith JB, Ortwerth BJ. Rapid assessment of early glycation products by mass spectrometry. Biochem Mol Biol Int 1996; 40: 315–25.
26. AD, Sheng H, Warner DS, et al. Hemodynamic effects of metalloporphyrin catalytic antioxidants: structure-activity relationships and species specificity. Free Radic Biol Med, 33, 2002, 1657–69.
<https://doi.org/10.1016/S0891-5849(02)01140-1>
27. H, Miyata S, Liu BF, et al. Inhibitory effects of tenilsetam on the Maillard reaction. Endocrinology 1997; 138: 1886–92.
<https://doi.org/10.1210/endo.138.5.5151>
28. FG, Pacher P, Mabley J, Liaudet L, Szabo C. Rapid reversal of the diabetic endothelial dysfunction by pharmacological inhibition of poly(ADP-ribose) polymerase. Circ Res 2001; 89: 684–91.
<https://doi.org/10.1161/hh2001.097797>
29. A. Oxidative stress induced cataract: mechanism of action. FASEB J 1995; 9: 1173.
<https://doi.org/10.1096/fasebj.9.12.7672510>
30. VS, Rouzer CA, Monnier VM, Cerami A. Diabetic cataract formation: potential role of glycosylation of lens crystallins. Proc Natl Acad Sci USA 1978; 75: 2918–22.
<https://doi.org/10.1073/pnas.75.6.2918>
<PubMed>
31. I. Glycation of albumin: reaction with glucose, fructose, galactose, ribose or glyceraldehyde measured using four methods. J Biochem Biophys Methods 1994; 28: 115–21.
<https://doi.org/10.1016/0165-022X(94)90025-6>
32. X, Sadeghi M, Olumee Z, Vertes A. Detection and quantification of β-2- microglobulin glycosylated end products in human serum by matrix-assisted laser desorption/ionization mass spectrometry. Anal Chem 1996; 68: 3740–5.
<https://doi.org/10.1021/ac960516u>
33. SR, Baynes JW. Role of the Maillard reaction in diabetes mellitus and diseases of aging. Drugs et Aging 1996; 9: 69–77.
<https://doi.org/10.2165/00002512-199609020-00001>
34. A, Van Campenhout Ch, Lagrou AR, Manuel-Y-Keenoy B. Effects of in vitro glycation on Fe3+ binding and Fe3+ isoforms of transferrin. Clin Chem 2004; 50: 1640–9.
<https://doi.org/10.1373/clinchem.2004.033811>
35. H, Brownlee M, Cerami A. Recognition and uptake of human diabetic peripheral nerve myelin by macrophages. Diabetes 1985; 34: 553–7.
<https://doi.org/10.2337/diab.34.6.553>
36. JL, Steinberg D. Role of oxidized low density lipoproteins in atherosclerosis. J Clin Invest 1991; 88: 1785–92.
<https://doi.org/10.1172/JCI115499>
<PubMed>
37. JS, Cooper MB, Gould BJ, Oughton J. Glycosylation and cross-linkage of cardiac myosin in diabetic subjects: A post-mortem study. Diabetes Medicine 1988; 5: 338–42.
<https://doi.org/10.1111/j.1464-5491.1988.tb01001.x>


