Hydroxyl radical mediates N-epsilon-(carboxymethyl)lysine formation from Amadori product

被引:157
|
作者
Nagai, R
Ikeda, K
Higashi, T
Sano, H
Jinnouchi, Y
Araki, T
Horiuchi, S
机构
[1] KUMAMOTO UNIV,SCH MED,DEPT BIOCHEM,KUMAMOTO 860,JAPAN
[2] KYUSHU TOKAI UNIV,FAC AGR,CHOYO ASO,KUMAMOTO 86914,JAPAN
关键词
D O I
10.1006/bbrc.1997.6608
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies demonstrated N-epsilon-(carboxymethyl) lysine (CML) in several tissue proteins, Incubation of proteins with glucose leads through a Schiff base to Amadori products. Oxidative cleavage of Amadori products is considered as a major route to CML formation in vivo, whereas it is not known which reactive oxygen species (ROS) is involved. The present study is undertaken to identify such a ROS. We prepared heavily glycated human serum albumin (HSA) which contained a high level of Amadori products, but an undetectable level of CML. Incubation of glycated HSA with FeCl2, but not with H2O2, led to CML formation which was enhanced by H2O2, but inhibited by catalase or mannitol, whereas superoxide dismutase had no effect, Similar data were obtained by experiments using Boc-fructose-lysine as a model Amadori compound, These data indicate that hydroxyl radical generated by the reaction of Fe2+ with H2O2 mediates CML formation from Amadori compounds. (C) 1997 Academic Press.
引用
收藏
页码:167 / 172
页数:6
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