Ameliorative Effects of Gallic Acid on Cisplatin-Induced Nephrotoxicity in Rat Variations of Biochemistry, Histopathology, and Gene Expression

• Published in: BioMed research international 2021, Vol.2021, p.2195238-11
• Main Authors: Eslamifar, Zahra, Moridnia, Abbas, Sabbagh, Susan, Ghaffaripour, Reza, Jafaripour, Leila, Behzadifard, Mahin
• Format: Article
• Language: English
• Subjects: Acids; Analysis; Animals; Antioxidants; Apoptosis; Biochemistry; Biomarkers - blood; Cancer; Care and treatment; Caspase 3 - analysis; Caspase 3 - genetics; Caspase-3; Cell cycle; Chemotherapy; Cisplatin; Cisplatin - pharmacology; Cisplatin - toxicity; Clusterin; Clusterin - analysis; Clusterin - genetics; Complications and side effects; Creatinine; Damage; Distilled water; Dosage and administration; Drug dosages; Gallic acid; Gallic Acid - pharmacology; Gene expression; Gene Expression - drug effects; Health aspects; Histopathology; Kidney - drug effects; Kidney - pathology; Kidney diseases; Kidney failure; Kidneys; Male; Oxidative stress; Oxidative Stress - drug effects; Parameters; Patient outcomes; Phenols; Physiological aspects; Prevention; Rats; Rats, Wistar; Reactive oxygen species; Reactive Oxygen Species - metabolism; Renal failure; Renal Insufficiency - drug therapy; Risk factors; Rodents; Side effects; Solid tumors; Toxicity; Tumors; Urea; Ureas; Uric acid; Variation
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2021/2195238

Background. Cisplatin is a powerful chemotherapeutic drug mainly used in the treatment of solid tumors. Aggregation of the drug in renal proximal tubule cells causes nephrotoxicity and renal failure. Investigations showed nephrotoxicity as Cisplatin’s dose-limiting side effect. One of the Cisplatin toxicity mechanisms is generation of reactive oxygen species, which leads to oxidative stress and renal damage. The purpose of this study was evaluation of the modulating effects of Gallic acid on Cisplatin-induced variations including Caspase-3 and Clusterin expression and histopathological and biochemical parameters in adult male Wistar rats. Method. Rats were kept under standard condition of temperature, light, and humidity. The animals were divided into 4 groups: GpI: control group (received distilled water for 10 days); GpII: Gallic acid (alone) (50 mg/kg bw, once a day for 10 days); GpIII: Cisplatin (alone), single dose (6 mg/kg bw, I.P. on 5th day of study); GpIV: Gallic acid (50 mg/kg bw, once a day for 10 days) and also injected with single dose of Cisplatin (6 mg/kg bw, I.P., on 5th day of study). After 10 days, all rats were anaesthetized and plasma collected to estimate urea, creatinine, and uric acid. The right kidneys were removed for the study of gene expression and biochemical parameters. The left kidneys were used for histopathological studies. Results. The Cisplatin-induced nephrotoxicity was evident from the elevated levels of creatinine, urea, uric acid, and renal tissue MDA and also decreased levels of SOD, CAT, GPX, and GSH in renal tissue. Administration of Gallic acid significantly modulated nephrotoxicity markers, gene expression variations, and histopathological damage. Conclusion. Outcomes of the present investigation suggest that Gallic acid provides protection against CP-induced nephrotoxicity, but for application in people, further studies are needed.