TY - JOUR AU - Parlak, Akif Evren AU - Karagozoglu, Yusuf AU - Alayunt, Naci O. AU - Turkoglu, Semra AU - Yildirim, Isil AU - Karatepe, Mustafa AU - Koparir, Metin PY - 2017/11/30 Y2 - 2024/03/29 TI - Biochemical evaluation of hydroxyurea derivative schiff bases in liver of rats JF - Cellular and Molecular Biology JA - Cell Mol Biol (Noisy-le-grand) VL - 63 IS - 11 SE - Original Research Articles DO - 10.14715/cmb/2017.63.11.2 UR - https://cellmolbiol.org/index.php/CMB/article/view/1422 SP - 5-10 AB - <p>In this study, it was aimed to examine the antioxidant and antihepatotoxic effects of hydroxyurea derivative Schiff bases on serum biochemical parameters (AST, ALT, LDH, urea, creatinine and total bilirubin) and antioxidant parameters (SOD, CAT, GPx, MDA). In this study, a total of 49 adult male Wistar rats was examined and they were divided into 7 equal groups. DMSO, which is diluted only with corn oil, was administered to control group. 25 mg / kg ligand, 25 mg / kg Schiff base - manganese, 25 mg / kg Schiff base-copper, 25 mg / kg Schiff base - zinc, 25 mg / kg Schiff base - nickel, 25 mg / kg Schiff base - cobalt complexes were administered to rats of experimental group subcutaneously for 15 days with three-day intervals throughout the test process. All specimens were killed by decapitation and their livers were extracted. According to the results obtained, ALT level was observed to be higher (P&lt;0.05) in the Cu-L group compared to other groups. LDH level was observed to be higher (P&lt;0.05) in the Cu-L and Co-L groups compared to other groups. SOD level was observed to be higher (P&lt;0.05) in the Cu-L, Mn-L and Zn-L groups compared to other groups. MDA level was observed to be higher (P&lt;0.05) in the Ni-L, Cu-L, Zn-L groups compared to other groups. In conclusion, it can be suggested that the determination of the pharmacological characteristics of them can be beneficial in numerous fields of application thanks to the antioxidant and hepatotoxic activities demonstrated by hydroxyurea derivative Schiff bases.</p> ER -