Research Information System
Indian Journal of Pharmaceutical Education and Research, vol.60, no.1, pp.410-420, 2026 (SCI-Expanded, Scopus)
Background: In the present study, we aimed to investigate the protective effect of Hydrogen sulfide (H2 S) donor Sodium Hydrosulphide (NaHS) and Sulfurized Apricot (SA) on experimental acute kidney injury induced by cisplatin in rats. Materials and Methods: Four groups of Wistar albino rats were formed with 10 rats in each group: Control group, Cisplatin group, Cisplatin+SA group, and Cisplatin+NaHS group. The activities of Superoxide Dismutase (SOD), Catalase (CAT), Glutathione Peroxidase (GPx) and Cystathione gamma-lyase (CSE), and the levels of Malondialdehyde (MDA), Glutathione (GSH) and total GSH were measured. Creatinine, urea, Sodium (Na), Chlorine (Cl), Potassium (K), Calcium (Ca), Aspartate aminotransferase (AST), and Alanine Aminotransferase (ALT) were also measured. Results: CAT activity increased in the cisplatin+SA and cisplatin+NaHS groups. CSE activity increased in the cisplatin+NaHS group. MDA levels increased in the cisplatin and cisplatin+NaHS groups. This increase was also observed in SOD and GPx activities but was not statistically significant. Serum ALT, AST, creatinine, and urea levels were higher in the cisplatin group. ADP activity was lower in the cisplatin group. The histological findings support the biochemical results obtained in our study. Red/total GSH was higher in the cisplatin, cisplatin+SA, and cisplatin+NaHS groups. Conclusion: SA and NaHS would have beneficial effects in preventing cisplatin-induced kidney damage.