Effects of carnosine and related compounds on monosaccharide autoxidation and H2O2 formation.
- Author:
Beom Jun LEE
1
;
Kyung Sun KANG
;
Sang Yoon NAM
;
Jae Hak PARK
;
Yong Soon LEE
;
Young Won YUN
;
Myung Haing CHO
Author Information
1. Laboratory of Veterinary Public Health, College of Veterinary Medicine, Seoul National University, Suwon, 441-744 South Korea.
- Publication Type:Original Article
- Keywords:
Carnosine and related compounds;
Glucose oxidation;
alpha-ketoaldehyde;
Free radicals;
Glycation;
Antioxidant
- MeSH:
Absorption;
Anserine;
beta-Alanine;
Carbohydrates;
Carnosine*;
Copper;
Diabetes Complications;
Free Radicals;
Fructosamine;
Furaldehyde;
Glucose;
Histidine;
Humans;
Lysine;
Serum Albumin
- From:The Korean Journal of Physiology and Pharmacology
1999;3(3):251-261
- CountryRepublic of Korea
- Language:English
-
Abstract:
The effects of carnosine and related compounds (CRCs) including anserine, homocarnosine, histidine, and beta-alanine on monosaccharide autoxidation and H2O2 formation were investigated. The incubation of CRCs with D-glucose, D-glucosamine, and D, L-glyceraldehyde at 37degreeC increased the absorption maxima at 285 nm, 273 nm, and 290 ~ 330 nm, respectively. D, L-glyceraldehyde was the most reactive sugar with CRCs. The presence of copper strongly stimulated the reaction of carnosine and anserine with D-glucose or D-glucosamine. Carnosine and anserine stimulated H2O2 formation from D-glucose autoxidation in a dose-dependent manner in the presence of 10 muM Cu (II). The presence of human serum albumin (HSA) decreased their effect on H2O2 formation. Carnosine and anserine has a biphasic effect on alpha-ketoaldehyde formation from glucose autoxidation. CRCs inhibited glycation of HSA as determined by hydroxymethyl furfural, lysine residue with free epsilon-amino group, and fructosamine assay. These results suggest that CRCs may be protective against diabetic complications by reacting with sugars and protecting glycation of protein.
