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Keywords: glycation
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Articles
Biochem Soc Trans (2014) 42 (2): 511–517.
Published: 20 March 2014
...Naila Rabbani; Fozia Shaheen; Attia Anwar; Jinit Masania; Paul J. Thornalley Glyoxalase- and methylglyoxal-related research has required the development of quantitative and reliable techniques for the measurement of methylglyoxal-derived glycation adducts of protein and DNA. There are also other...
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Biochem Soc Trans (2014) 42 (2): 518–522.
Published: 20 March 2014
... is glycation that occurs when reducing sugars react non-enzymatically with proteins. This reaction also happens when the dicarbonyl compounds GO (glyoxal) and MG (methylglyoxal), which are glucose derivatives, react with proteins. These compounds can be detoxified by the glyoxalase system composed of two...
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Biochem Soc Trans (2014) 42 (2): 413–418.
Published: 20 March 2014
... of enzymatic defence against dicarbonyl glycation, particularly by endogenous methylglyoxal, now seems secure. We are now in an era of investigation of the regulation of the glyoxalase system where a role in aging and disease, physiological stress and drug resistance and development of healthier foods and new...
Articles
Biochem Soc Trans (2014) 42 (2): 457–460.
Published: 20 March 2014
...Reiko Inagi Glycation is one of the important reactions regulating physiological state, and glycative stress, namely an overwhelming and unfavourable glycation state, is established as a pathological factor. Glycative stress is closely associated with not only various kidney diseases, but also...
Articles
Biochem Soc Trans (2014) 42 (2): 495–499.
Published: 20 March 2014
...Mingzhan Xue; Naila Rabbani; Paul J. Thornalley The glyoxalase system is an important component of the enzymatic defence against glycation, preventing particularly quantitatively and functionally important glycation of protein and DNA by methylglyoxal. Expression of genes encoding Glo1 (glyoxalase...
Articles
Biochem Soc Trans (2014) 42 (2): 425–432.
Published: 20 March 2014
...Naila Rabbani; Paul J. Thornalley Methylglyoxal is a potent protein-glycating agent. It is an arginine-directed glycating agent and often modifies functionally important sites in proteins. Glycation forms mainly MG-H1 [ N δ -(5-hydro-5-methyl-4-imidazolon-2-yl)ornithine] residues. MG-H1 content...
Articles
Biochem Soc Trans (2014) 42 (2): 538–542.
Published: 20 March 2014
... of antibodies against cyclic citrullinated peptide, identified as a screening marker and marker of disease progression, has been proposed. Studies of glycation in arthritis have focused mostly on levels of AGEs (advanced glycation end-products), N ε -carboxymethyl-lysine and pentosidine. There was a weak...
Articles
Biochem Soc Trans (2014) 42 (2): 504–510.
Published: 20 March 2014
... interference in methylglyoxal and glyoxal estimations. This interference is blocked by the addition of sodium azide in the derivatizing buffer. Estimates of methylglyoxal concentration thereby obtained are in keeping with those predicted by systems modelling of methylglyoxal glycation kinetics in situ...
Articles
Biochem Soc Trans (2008) 36 (5): 1045–1050.
Published: 19 September 2008
...Naila Rabbani; Paul J. Thornalley Protection of mitochondrial proteins from glycation by endogenous dicarbonyl compounds, methylglyoxal and glyoxal, was found recently to prevent increased formation of reactive oxygen species and oxidative and nitrosative damage to the proteome during aging...
Articles
Biochem Soc Trans (2007) 35 (5): 853–856.
Published: 25 October 2007
... cardiovascular function. Physiologically, collagen and elastin fibres are enzymatically cross-linked to form matrix. In addition to these enzymatically formed cross-links, collagen fibres may be linked non-enzymatically, most notably by formation of AGEs (advanced glycation end-products). AGEs are formed...
Articles
Biochem Soc Trans (2003) 31 (6): 1367–1371.
Published: 01 December 2003
...M.J.C. Crabbe Kinetic studies on the AR (aldose reductase) protein have shown that it does not behave as a classical enzyme in relation to ring aldose sugars. As with non-enzymatic glycation reactions, there is probably a free-radical element involved derived from monosaccharide autoxidation...
Articles
Biochem Soc Trans (2003) 31 (6): 1409–1412.
Published: 01 December 2003
...A. Ponces Freire; A. Ferreira; R. Gomes; C. Cordeiro Saccharomyces cerevisiae is an outstanding cellular model for metabolic studies in glycation. Due to its high glycolytic activity, it produces methylglyoxal, a highly reactive intracellular glycation agent, at a rate of approx. 0.1...
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Biochem Soc Trans (2003) 31 (6): 1341–1342.
Published: 01 December 2003
...P.J. Thornalley Glycation of proteins, nucleotides and basic phospholipids by glucose, glyoxal, methylglyoxal, 3-deoxyglucosone and other saccharide derivatives is potentially damaging to the proteome and mutagenic. It is now recognized that there is an enzymatic defence against glycation – a group...
Articles
Biochem Soc Trans (2003) 31 (6): 1343–1348.
Published: 01 December 2003
... spontaneously from α-oxoaldehyde and GSH, to S -2-hydroxyacylglutathione derivatives [RCOCH(OH)-SG→RCH(OH)CO-SG], and in so doing decreases the steady-state concentrations of physiological α-oxoaldehydes and associated glycation reactions. Physiological substrates of glyoxalase I are methylglyoxal, glyoxal...
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Biochem Soc Trans (2003) 31 (6): 1349–1353.
Published: 01 December 2003
... far. For this reason, introduction of deglycating enzymes as anti-aging strategy would be desirable. This article provides an update on amadoriase enzymes from fungi which, one day, will hopefully help prevent the in vivo consequences of glycation. 1 To whom correspondence should be addressed (e...
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Biochem Soc Trans (2003) 31 (6): 1354–1357.
Published: 01 December 2003
...G. Delpierre; E. Van Schaftingen The in vivo formation of fructosamines following non-enzymatic reaction of proteins with glucose (i.e. glycation) was first described almost 30 years ago. Until recently, the only known fate of fructosamines in mammalian cells was their spontaneous conversion...
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Biochem Soc Trans (2003) 31 (6): 1433–1437.
Published: 01 December 2003
... of the F3K pathway by feeding glycated casein causes an increase of 10–20-fold in plasma levels of 3DG and 3-fold in kidney tubules. Consequences of this increase were studied in two systems: the Eker rat, a model of susceptible kidney tubules; and birth rates in two rat strains. In both cases substantial...
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Biochem Soc Trans (2003) 31 (6): 1358–1363.
Published: 01 December 2003
...P.J. Beisswenger; S.K. Howell; R.G. Nelson; M. Mauer; B.S. Szwergold The factors responsible for variable susceptibility to diabetic nephropathy are not clear. According to the non-enzymatic glycation hypothesis, diabetes-related tissue damage occurs due to a complex mixture of toxic products...
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