The effect of nimesulide on oxidative damage inflicted by ischemia-reperfusion on the rat renal tissue

Ren Fail. 2015 Mar;37(2):323-31. doi: 10.3109/0886022X.2014.985996. Epub 2014 Nov 24.

Abstract

The objective of our study is to research biochemically and histopathologically the effect of nimesulide on oxidative damage inflicted by ischemia-reperfusion (I/R) on the rat renal tissue. Twenty-four albino Wistar type of male rats were used for the experiment. The animals were divided into groups as: renal ischemia-reperfusion control (RIR), nimesulide+renal ischemia-reperfusion of 50 mg/kg (NRIR-50), nimesulide+renal ischemia-reperfusion of 100 mg/kg (NRIR-100), and sham groups (SG). In NRIR-50 and NRIR-100 groups were given nimesulide, and RIR and SG groups were given distilled water, an hour after anesthesia. Groups, except for the SG group, 1-h-ischemia and then 6-h-reperfusion were performed. In the renal tissue of the RIR group in which the malondialdehyde (MDA), myeloperoxidase (MPO), and 8-hydroxyguanine (8-OHGua) levels were measured, the COX-1 and COX-2 activities were recorded. Nimesulide at 100 mg/kg doses reduced the oxidant parameters more significantly than 50 mg/kg doses; on the other hand, it raised the antioxidant parameters. It has been shown that 100 mg/kg doses of nimesulide prevented the renal I/R damage more significantly than a dose of 50 mg/kg, which shows that nimesulide, in clinics, could be used in the prevention of I/R damage.

Keywords: Ischemia; nimesulide; rat; renal; reperfusion.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Dose-Response Relationship, Drug
  • Kidney / pathology
  • Kidney Diseases* / drug therapy
  • Kidney Diseases* / etiology
  • Kidney Diseases* / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Oxidative Stress / drug effects*
  • Peroxidase / metabolism
  • Platelet Aggregation Inhibitors / pharmacology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Rats
  • Rats, Wistar
  • Reperfusion Injury* / drug therapy
  • Reperfusion Injury* / metabolism
  • Sulfonamides / pharmacology*
  • Time Factors
  • Treatment Outcome

Substances

  • Antioxidants
  • Platelet Aggregation Inhibitors
  • Sulfonamides
  • Malondialdehyde
  • Peroxidase
  • Prostaglandin-Endoperoxide Synthases
  • nimesulide