T. Niwa et al., IMIDAZOLONE, A NOVEL ADVANCED GLYCATION END-PRODUCT, IS PRESENT AT HIGH-LEVELS IN KIDNEYS OF RATS WITH STREPTOZOTOCIN-INDUCED DIABETES, FEBS letters, 407(3), 1997, pp. 297-302
We produced a monoclonal antibody to imidazolones A and B, novel advan
ced glycation end products formed from the reaction of 3-deoxyglucoson
e (3-DG) with the guanidino group of arginine. Liquid chromatography/m
ass spectrometry demonstrated that the formation of imidazolone A by i
ncubating 3-DG with arginine is very rapid, reaching a maximum concent
ration within 24 h, but the formation of imidazolone B is very slow an
d low in quantity even after 2 weeks. Thus, at physiological condition
s the formation of imidazolone A is dominant, while that of imidazolon
e B is negligible. Immunochemistry demonstrated that the imidazolone c
ontent in the kidneys of streptozotocin-induced diabetic rats was sign
ificantly higher than in the control rats. Serum levels of 3-DG in the
diabetic rats were also significantly higher than in control rats. 3-
DG attacks the arginine residues of the tissue proteins, producing imi
dazolone at high levels in the kidneys affected by diabetic nephropath
y. (C) 1997 Federation of European Biochemical Societies.