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International Journal of Pharmacology

Year: 2011 | Volume: 7 | Issue: 6 | Page No.: 697-703
DOI: 10.3923/ijp.2011.697.703

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Authors


Iman Abdelaziz

Country: Egypt

Mahmoud Kandeel

Country: Egypt

Keywords


  • Nigella sativa
  • Allium sativum
  • lesion scoring
  • oxidative stress
  • Amikacin, nephrotoxicity
Research Article

The Protective Effects of Nigella sativa Oil and Allium sativum Extract on Amikacin-induced Nephrotoxicity

Iman Abdelaziz and Mahmoud Kandeel
Amikacin is a valuable aminoglycoside in serious infections. However, its use is associated with undesirable renal toxicity. This study was designed to check the effect of Nigella sativa oil and Allium sativum extract in ameliorating amikacin-induced renal damage by using a rat model of nephrotoxicity. Rats received nephrotoxic dose of amikacin and the amelioration of amikacin-induced nephrotoxicity was assessed through microscopic lesion scoring of damaged renal tissue and estimating the changes in biomarkers of tissue damage. Nigella sativa oil and Allium sativum extract significantly decreased the levels of NO, malondialdehyde and total antioxidant capacity. Furthermore, they increased the level of reduced glutathione. These changes are indicative for lower tissue damage and reduced free radical formation. These results were coinciding with the lower levels of urea, uric acid and creatinine (which were significantly elevated in amikacin treated groups). Semi-quantitative analysis of cellular infiltration, necrosis of tubular cells and tubular cellular damage indicated the protective effect of the used plant materials in reducing renal damage induced by amikacin. By using a rat model, Nigella sativa oil and Allium sativum extract efficiently ameliorated the renal toxic effect of amikacin. Further studies are required for applications in other animals or human subjects.
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How to cite this article

Iman Abdelaziz and Mahmoud Kandeel, 2011. The Protective Effects of Nigella sativa Oil and Allium sativum Extract on Amikacin-induced Nephrotoxicity. International Journal of Pharmacology, 7: 697-703.

DOI: 10.3923/ijp.2011.697.703

URL: https://scialert.net/abstract/?doi=ijp.2011.697.703

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