Overexpression of Glyoxalase-I Reduces Hyperglycemia-induced Levels of Advanced Glycation End Products and Oxidative Stress in Diabetic Rats
Glycation End Products, Advanced
0301 basic medicine
571
Social and Behavioral Sciences
Gene Expression Regulation, Enzymologic
Oxidative Phosphorylation
Diabetes Mellitus, Experimental
03 medical and health sciences
Pregnancy
Methylglyoxal
Medicine and Health Sciences
Animals
Humans
Endothelium
Rats, Wistar
Glycation
Diabetes
Lactoylglutathione Lyase
Glyoxal
Pyruvaldehyde
Glyoxalase-1
Mitochondria
Rats
3. Good health
Disease Models, Animal
Oxidative Stress
Metabolism
Oxidative stress
Hyperglycemia
Rat
Female
Rats, Transgenic
Biomarkers
DOI:
10.1074/jbc.m110.144097
Publication Date:
2010-11-06T01:10:37Z
AUTHORS (10)
ABSTRACT
The reactive advanced glycation end product (AGE) precursor methylglyoxal (MGO) and MGO-derived AGEs are associated with diabetic vascular complications and also with an increase in oxidative stress. Glyoxalase-I (GLO-I) transgenic rats were used to explore whether overexpression of this MGO detoxifying enzyme reduces levels of AGEs and oxidative stress in a rat model of diabetes. Rats were made diabetic with streptozotocin, and after 12 weeks, plasma and multiple tissues were isolated for analysis of AGEs, carbonyl stress, and oxidative stress. GLO-I activity was significantly elevated in multiple tissues of all transgenic rats compared with wild-type (WT) littermates. Streptozotocin treatment resulted in a 5-fold increase in blood glucose concentrations irrespective of GLO-I overexpression. Levels of MGO, glyoxal, 3-deoxyglucosone, AGEs, and oxidative stress markers nitrotyrosine, malondialdehyde, and F2-isoprostane were elevated in the diabetic WT rats. In diabetic GLO-I rats, glyoxal and MGO composite scores were significantly decreased by 81%, and plasma AGEs and oxidative stress markers scores were significantly decreased by ∼50%. Hyperglycemia induced a decrease in protein levels of the mitochondrial oxidative phosphorylation complex in the gastrocnemius muscle, which was accompanied by an increase in the lipid peroxidation product 4-hydroxy-2-nonenal, and this was counteracted by GLO-I overexpression. This study shows for the first time in an in vivo model of diabetes that GLO-I overexpression reduces hyperglycemia-induced levels of carbonyl stress, AGEs, and oxidative stress. The reduction of oxidative stress by GLO-I overexpression directly demonstrates the link between glycation and oxidative stress.
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CITATIONS (188)
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