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Selenium Nanoparticles Attenuate Gentamycin-Induced Nephrotoxicity and Hematotoxicity in Female Swiss Albino Mice

  • Faouzi DahdouhEmail author
  • Hacene Bendjeffal
  • Zakaria Nouacer
  • Walid Moumene
  • Mohamed El-Hadi Zeminour
  • Mohamed Naous
  • Houria Djebar
Article

Abstract

Gentamycin (GM) is a widely used antibiotic for the treatment of Gram-negative bacterial infections, but nephrotoxic effects limit its use. Selenium nanoparticles (SeNPs) have attracted worldwide research interest due to their high bioavailability and potential antioxidant property. This study was, therefore, designed to examine the protective effect of SeNPs on GM-induced changes in body and kidney weights, blood hematology, serum biochemistry parameters, and renal tissue markers of oxidative stress in female mice. GM was administered intraperitoneally (100 mg/kgb.w) and SeNPs were given by oral gavage (2 mg/kg b.w) for 10 consecutive days. GM treatment caused significant changes in the body and relative kidney weights and significant renal damage, evidenced by increased serum levels of urea, uric acid, creatinine, total proteins, and blood urea nitrogen (BUN), along with noteworthy histopathological alterations. A marked decrease in serum sodium and potassium ions, and kidney tissue antioxidative defense system (reduced glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT)) was observed in GM-treated mice when compared with the normal mice. Furthermore, significant decrease in total white blood corpuscles (WBC) count, total platelets count (PLT), total red blood corpuscles (RBC) count, hemoglobin concentration (Hgb), and packed cell volume (PCV) was also revealed in GM-treated group. However, GM + SeNPs group had effectively reversed GM-induced alteration of both biochemical and renal histological structures. Our results suggested for the first time that SeNPs are potent antioxidant candidate against GM-induced oxidative kidney toxicity and hematoxicity in mice.

Keywords

Gentamycin Hematotoxicity Mice Renal toxicity Histopathology Selenium nanoparticles 

Notes

Acknowledgements

The authors express their appreciation to Dr. Azzouz Zoubir and Dr. Tichiti Lazhari of Annaba University for the valuable assistance.

Compliance with Ethical Standards

Conflicts of Interest

The authors declare that they have no conflict of interest.

Ethical Approval

All experimental procedures were approved by the Animal Care Committee and Ethics Committee of our institution (AFRO. No 478, 2009).

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© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Faouzi Dahdouh
    • 1
    • 2
    Email author
  • Hacene Bendjeffal
    • 3
    • 4
  • Zakaria Nouacer
    • 1
  • Walid Moumene
    • 1
  • Mohamed El-Hadi Zeminour
    • 1
  • Mohamed Naous
    • 5
  • Houria Djebar
    • 1
  1. 1.Laboratory of Cell Toxicology, Department of BiologyBadji Mokhtar, Annaba UniversityAnnabaAlgeria
  2. 2.Department of Natural Sciences, Higher School of Professors for Technological EducationSkikdaAlgeria
  3. 3.Laboratory of water treatment and valorization of industrial wastes, Department of ChemistryBadji Mokhtar, Annaba UniversityAnnabaAlgeria
  4. 4.Department of Physics and Chemistry, Higher School of Professors for Technological EducationSkikdaAlgeria
  5. 5.Laboratory of Macromolecular Chemistry and PhysicsUniversity of Oran1 Ahmed BenbellaOranAlgeria

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