Aktay, GTozkoparan, BErtan, M2024-08-042024-08-0420050253-6269https://doi.org/10.1007/BF02977673https://hdl.handle.net/11616/94019A series of 3-[1-(4-(2-methyIpropyl) phenyl) ethyl] - 1 2,4-triazole-5-th ion e (1) and its bicyclic condensed derivatives 6-benzylidenethiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones (IIa-IIf) were investigated for the prevention of ethanol-induced oxidative stress in liver and brain of mice. Administration of ethanol (0.1 mL/mice, p.o.) resulted in a drop of total thiol groups (T-SH) and non-protein thiol groups (NP-SH), and an increase in thiobarbituric acid reactive substances (TBARS) in both liver and brain tissue of mice (p < 0.001). Among the compounds investigated (at a dose of 200 mg/kg, p.o.), I and IId ameliorated the peroxidative injury in these tissues effectively. Compounds IIa, IIc and IIe improved the peroxidative tissue injury only in brain. These findings suggest that certain condensed thiazolo-triazole compounds may contribute to the control of ethanol-induced oxidative stress in an organ selective manner.eninfo:eu-repo/semantics/closedAccessantioxidant activitycondensed thiazolo-triazole compoundsethanol toxicitynon-steroidal antiinflammatory drugsoxidative stressProtective effects of thiazolo[3,2-b]-1,2,4-triazoles on ethanol-induced oxidative stress in mouse brain and liverArticle2844384421591851710.1007/BF029776732-s2.0-22844445903N/AWOS:000228809700010Q4