Detection and determination of glyceraldehyde-derived advanced glycation end product

被引:8
|
作者
Usui, T
Shimohira, K
Watanabe, H
Hayase, F
机构
[1] Meiji Univ, Fac Agr, Dept Agr Chem, Tama Ku, Kanagawa 2148571, Japan
[2] Meiji Univ, Fac Agr, Dept Life Sci, Tama Ku, Kanagawa 2148571, Japan
关键词
D O I
10.1002/biof.552210176
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
Protein is modified by carbonyl compound in the Maillard reaction, and the irreversible structure is formed as the advanced glycation end product (AGE). We identified GLAP (glyceraldehyde-derived pyridinium compound) as an AGE formed from glyceraldehyde and lysine residue of protein. In the present study, we investigated detection and determination of GLAP from glycated protein using fluorescence HPLC method. Albumin (BSA) and carbonyls (glyceraldehyde, glycolaldehyde, methylglyoxal, glyoxal, three pentoses or three hexoses) were dissolved in phosphate buffed solution (pH 7.4), and incubated at 37degreesC for a week. GLAP was formed only in the glyceraldehyde-modified BSA. It is suggested that GLAP was specific AGE derived from glyceraldehyde. In addition, GLAP depressed the intracellular glutathione level and induced the reactive oxygen species (ROS) in HL-60 cells. GLAP caused the oxidative stress. Therefore, GLAP will be a biomarker in the AGE related disease such as diabetic complications or chronic renal failure.
引用
收藏
页码:391 / 394
页数:4
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