Two different markers of oxidative protein damage in plasma of alloxan-induced hyperglycemic rabbits: effects of pioglitazone and repaglinide. Oxidative protein damage and two antidiabetics
DOI:
https://doi.org/10.12923/j.2084-980X/25.2/a.01Keywords:
experimental hyperglycemia, oxidative/nitrosative stress, oxidized proteins, antidiabeticsAbstract
Reactive oxygen and nitrogen species are known to contribute to different pathological alterations in hyperglycemic state. Especially proteins are major targets resulting from their rapid reactions with many oxidants. Therefore, the present study was undertaken to examine some common markers of oxidative/nitrosative stress in plasma of alloxan-induced hyperglycemic rabbits with special regard to protein oxidation. The second goal was to investigate which of two antidiabetics, pioglitazone from peroxisome proliferator-activated receptor gamma agonists, and repaglinide from non-sulfonylurea KATP channel blockers, could be more effective in ameliorating these oxidative/nitrosative changes. In our hyperglycemic animals glutathione decreased by 41% as compared to control group. Simultaneously, lipid peroxidation products increased by 62%, nitrites by 59%, protein carbonyl groups by 71% and advanced oxidized protein products by 53%. In hyperglycemic-treated animals pioglitazone increased glutathione above control values. In turn, lipid peroxidation was reduced by 29%, nitrites by 22%, advanced oxidized protein products by 37% and protein carbonyl groups by 42% in relation to hyperglycemic-non treated rabbits. After repaglinide treatment, lipid peroxidation decreased by 17% but the levels of glutathione, nitrites and both markers of oxidized proteins, were not affected. Our results confirmed that the action of pioglitazone is more comprehensive than that of repaglinide, independently of their action on hyperglycemia.
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