African Journal of
Pharmacy and Pharmacology

  • Abbreviation: Afr. J. Pharm. Pharmacol.
  • Language: English
  • ISSN: 1996-0816
  • DOI: 10.5897/AJPP
  • Start Year: 2007
  • Published Articles: 2284

Full Length Research Paper

The protective effect of silymarin on the antioxidant system at rat renal ischemia/reperfusion injury model

Ayhanci Adnan1, Ozkal Bilge1, Kabay Sahin2*, Burukoglu Dilek3, Guven Gül4, Bayramoglu Gökhan1, Senturk Hakan1, Ustuner M Cengiz5, Akyuz Fahrettin6 and Ozden Hilmi, MD4
1Department of Biology, Faculty of Art and Science, Osmangazi University, Turkey. 2Department of Urology, Faculty of Medicine, Dumlupinar Univeristy, Turkey. 3Department of Histology and Embriology, Faculty of Medicine, Osmangazi University,Turkey. 4Department of Anatomy, Faculty of Medicine, Osmangazi University, Turkey. 5Department of Medical Biology, Faculty of Medicine, Osmangazi University, Turkey. 6Department of Biochemistry, Faculty of Medicine, Osmangazi University, Turkey.
Email: [email protected]

  •  Accepted: 10 August 2012
  •  Published: 15 February 2013

Abstract

The aim of this study is to reveal the protective effects of silymarin (SM) treatment on the generation of oxidative stress with rat renal ischemia/reperfusion (I/R) injury model. Thirty-two (32) Sprague-Dawley rats were evaluated in four groups. Group I (Sham), Group II (renal I/R), Group III (renal I/R injury + SM 100 mg per kg) and Group IV (renal I/R injury + SM 200 mg per kg) were designed to evaluate dose-dependent effects of SM in renal I/R injury on the morphological and biochemical parameters changes. Renal I/R significantly decreased the enzymatic activity of catalase (CAT) and superoxide dismutase (SOD), whereas the malondialdeyde (MDA) levels increased. After renal I/R injury, significant tubular dilatation, tubular necrosis, glomerular necrosis, tubular vacuolization, hyaline casts, interstitial inflammation and necrosis of epithelium due to I/R injury was observed. In the Groups III and IV, in which the rats were treated with SM before renal I/R, tubular dilatation, tubular necrosis, glomerular necrosis, tubular vacuolization, hyaline casts, interstitial inflammation and necrosis of epithelium due to I/R injury were observed to be significantly protected with the treatment.The results of this study have demonstrated that SM significantly prevents the generation of oxidative stress and renal I/R injury induced renal changes in the rat.

 

Key words: Kidney, oxidative stress, pathology, rat, silymarin, morphology.