Quantification of oxidative stress markers in the blood sera following subacute administration of different oximes in rats
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38992768
DOI
10.1016/j.cbi.2024.111138
PII: S0009-2797(24)00284-9
Knihovny.cz E-zdroje
- Klíčová slova
- Blood sera, Oxidative stress, Oximes, Rats, Subacute toxicity,
- MeSH
- antioxidancia metabolismus farmakologie MeSH
- biologické markery * krev MeSH
- glutathion * krev metabolismus MeSH
- katalasa metabolismus krev MeSH
- krysa rodu Rattus MeSH
- malondialdehyd krev metabolismus MeSH
- oxidační stres * účinky léků MeSH
- oximy * farmakologie MeSH
- peroxidace lipidů účinky léků MeSH
- potkani Wistar * MeSH
- produkty pokročilé oxidace proteinů krev MeSH
- reaktivátory cholinesterasy farmakologie MeSH
- superoxiddismutasa metabolismus krev MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antioxidancia MeSH
- biologické markery * MeSH
- glutathion * MeSH
- katalasa MeSH
- malondialdehyd MeSH
- oximy * MeSH
- produkty pokročilé oxidace proteinů MeSH
- reaktivátory cholinesterasy MeSH
- superoxiddismutasa MeSH
Oxidative stress status, as a disruption of redox homeostasis, in the blood sera of Wistar rats caused by repeated application of selected acetylcholinesterase reactivators - asoxime, obidoxime, K027, K048, K074, and K075 were evaluated. Throughout this study, each oxime in a dose of 0.1 of LD50/kg im was given 2x/week for 4 weeks. Then, seven days after the last oximes' application, markers of lipid peroxidation (malondialdehyde, MDA), and protein oxidation (advanced oxidation protein products, AOPP), as well as the activity of antioxidant enzymes (catalase, CAT, superoxide dismutase, SOD, reduced glutathione, GSH, and oxidized glutathione, GSSG), were determined. Oxidative stress parameters, MDA and AOPP were significantly highest in the K048-, K074- and K075-treated groups (p < 0.001). The activity of CAT was significantly elevated in the obidoxime-treated group (p < 0.05), while treatment with K027, K048, and K074 induced high elevation in SOD levels (p < 0.01, p < 0.001). Interestingly, the activity of GSH in each oxime-treated group was significantly elevated. Unlike, treatment with obidoxime caused elevation in GSSG levels (p < 0.01). As a continuation of our previously published data, these results assure that applied oximes following subacute treatment ameliorated the oxidative status and further adverse systemic toxic effects in rats.
Special Police Unit Ministry of Interior Trebevićka 12 A 11 030 Belgrade Serbia
Veterinary Services Center Military Health Department Crnotravska 17 11040 Belgrade Serbia
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