protective effect of pomegranate seed oil against acute toxicity of diazinon in rat kidney

Authors

mohammad taher boroushaki 1- pharmacological research center of medicinal plants, faculty of medicine, mashhad university of medical sciences, mashhad, iran. 2- deptartment of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran.

delnia arshadi deptartment of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran.

hamideh jalili-rasti deptartment of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran.

elham asadpour deptartment of pharmacology, faculty of medicine, mashhad university of medical sciences, mashhad, iran.

abstract

diazinon is an organophosphate which is extensively used in trade and agriculture. due to its widespread application, its toxicity is common. several studies have shown that organophosphates are able to induce oxidative stress by generating free radicals and depletion of endogenous antioxidants. pomegranate seed oil (pso) possesses anti-inflammatory and antioxidant effects. in this study, the effect of pso was evaluated on diazinon-induced nephrotoxicity in rat. wistar male rats were randomly divided into four groups, 6 each. group one received saline, 1 ml/kg, group 2 received diazinon 100 mg/kg. groups 3 and 4 received pso, 0.32 and 0.64 mg/kg, one hour before diazinon 100 mg/kg respectively. after 24 h, animals were anesthetized. blood samples were taken out by cardiac puncture for measuring the level of serum urea and creatinine. 24 h urine samples were also collected for measuring glucose and protein concentration. the right kidney was removed and homogenized for measuring malondialdehyde and thiol content compare to control group, diz increased urea and serum creatinine, urinary glucose, and malondialdehyde, but did not modify significantly urinary protein and thiol content. in groups received pso+ diz, serum creatinine, urinary glucose and mda were significantly decreased. diz induced acute nephrotoxicity and oxidative stress. probably, increasing of serum creatinine and urinary glucose are appropriate markers for diagnosis of kidney damage. in addition increasing of mda level emphasizes that diz plays role in pathogenesis of kidney via oxidative stress mechanism. pso reduced diz toxicity by antioxidant activity.

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Journal title:
iranian journal of pharmaceutical research

جلد ۱۲، شماره ۴، صفحات ۸۲۱-۸۲۷

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