ZINC OXIDE NANOPARTICLES AMELIORATE ALUMINUM CHLORIDE-INDUCED HEPATO-RENAL OXIDATIVE STRESS AND INFLAMMATION IN RATS

Authors

  • SAHAR M. MAHMOUD Assistant Professor of Physiology at Department of Zoology, Faculty of Science, Cairo University, Cairo, Egypt
  • RAMI B. KASSAB Assistant Professor of Physiology at Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt
  • AHMED E. ABDEL MONEIM Professor of Physiology at Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt

DOI:

https://doi.org/10.22159/ijpps.2020v12i1.35956

Keywords:

Zinc nanoparticles, Aluminum, Inflammation, Oxidative stress, Liver, Kidney

Abstract

Objective: The present study was designed to evaluate the effect of zinc oxide nanoparticles (ZnO NPs) on Aluminum chloride (AlCl3)-induced hepato-renal injury. 

Methods: Animals were divided into, I-control group; rats received saline, II-AlCl3 group; animals received 100 mg AlCl3/kg body weight, III-ZnO NPs group; rats received 10 mg ZnO NPs/kg body weight, and IV group ZnO NPs+AlCl3. All rats were administered their respective doses daily for 6 w. Hepatorenal function parameters in sera; aminotransferases, bilirubin, urea, and creatinine were estimated. Lipid peroxide level and nitrite\nitrate ratio, glutathione content, glutathione peroxidase, glutathione reductase, catalase, superoxide dismutase activities and interleukin-1β, tumor necrosis factor-α levels were determined in both tissues. The histopathological and the immunohistochemical investigations of nuclear factor-kB expression were carried out. 

Results: ZnO NPs treatment to AlCl3-intoxicated rats significantly reduced Al accumulation (at p<0.05) in the hepatorenal tissue and increased zinc accumulation (at p<0.05) in liver and kidney, respectively, with respect to AlCl3-group, thus inhibiting oxidative stress and inflammation parameters represented by lipid peroxidation and nitric oxide levels (at p<0.05) compared to AlCl3 group and elevated antioxidant parameters (at p<0.05), compared to AlCl3 treated group, while suppressed interleukin-1β, tumor necrosis factor-α levels (at p<0.05) and the nuclear factor-kB activation in liver and kidney, especially in the kidney if compared to AlCl3-treated group. Hepatorenal function indices indicated significant decreases compared to AlCl3 group (at p<0.05).

Conclusion: Results indicated the ameliorative effect of ZnO NPs on aluminum-induced hepato-renal damage.

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Published

01-01-2020

How to Cite

MAHMOUD, S. M., R. B. KASSAB, and A. E. A. MONEIM. “ZINC OXIDE NANOPARTICLES AMELIORATE ALUMINUM CHLORIDE-INDUCED HEPATO-RENAL OXIDATIVE STRESS AND INFLAMMATION IN RATS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 12, no. 1, Jan. 2020, pp. 11-20, doi:10.22159/ijpps.2020v12i1.35956.

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