Zinc Oxide Nanoparticles Ameliorate Dimethylnitrosamine-Induced Renal Toxicity in Rat

• Published in: Applied biochemistry and biotechnology Vol. 194; no. 4; pp. 1699 - 1715
• Main Authors: Rani, Varsha, Verma, Yeshvandra, Rana, S. V. S.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.04.2022; Springer Nature B.V
• Subjects: Animal models; Animals; Antioxidants - pharmacology; Biochemistry; Biotechnology; Body Weight; Carcinogens; Chemistry; Chemistry and Materials Science; Dimethylnitrosamine - pharmacology; DNA damage; Glutathione; Glutathione peroxidase; Glutathione transferase; Hydrogen peroxide; Hydrogen Peroxide - pharmacology; Immune system; Immunosuppressive agents; Kidneys; Malondialdehyde; N-Nitrosodimethylamine; Nanoparticles; Organs; Original Article; Oxidation; Oxidative Stress; Peroxidase; Rats; Toxicity; Zinc oxide; Zinc Oxide - toxicity; Zinc oxides; Oxidative stress; Histopathology; Dimethylnitrosamine; Kidney; Zinc oxide nanoparticles
• ISSN: 0273-2289; 1559-0291
• DOI: 10.1007/s12010-021-03689-4

Dimethylnitrosamine (DMN) is an established carcinogen. It is toxic to several organs, viz., the liver, kidney, and lungs, and immune system. Several drugs have been used in the past to modulate its toxicity using experimental animal models. The present study was designed to investigate the effect of zinc oxide nanoparticles (ZnONPs) on renal toxicity caused by DMN in laboratory rat. Since oxidative mechanisms are mainly involved in its toxicity, the proposed study focuses on the amelioration of oxidative stress response by ZnONPs, if any. The present results show that administration of ZnONPs (50 mg/kg body weight/rat) to DMN (2 μl/100 g body weight/rat)-treated rats diminuted the concentration of malonaldehyde, H 2 O 2 , and NO in the kidney. However, reduced glutathione (GSH) concentration increased after ZnONP treatment. Results on glutathione S-transferase and glutathione peroxidase favored its antioxidative effects. These results are supported by the recovery of oxidative DNA damage and less pronounced histopathological changes in the kidney. It is hypothesized that ZnONPs might be toxic to renal tissue; however, its strong therapeutic/antioxidative potential helps in ameliorating DMN-induced renal toxicity in rat.