Protective effect of pomegranate seed oil against cisplatin-induced nephrotoxicity in rat

被引:22
|
作者
Boroushaki, Mohammad Taher [1 ]
Rajabian, Arezoo [2 ]
Farzadnia, Mehdi [2 ,3 ]
Hoseini, Azar [1 ]
Poorlashkari, Mojdeh [4 ]
Taghavi, Amin [5 ]
Dolati, Karim [2 ]
Bazmandegan, Gholamreza [2 ]
机构
[1] Mashhad Univ Med Sci, Fac Med, Pharmacol Res Ctr Med Plants, Mashhad, Iran
[2] Mashhad Univ Med Sci, Fac Med, Dept Pharmacol, Mashhad, Iran
[3] Mashhad Univ Med Sci, Fac Med, Imam Reza Hosp, Canc Mol Pathol Res Ctr, Mashhad, Iran
[4] Rafsanjan Univ Med Sci, Fac Med, Dept Pathol, Rafsanjan, Iran
[5] Rafsanjan Univ Med Sci, Fac Med, Rafsanjan, Iran
关键词
Cisplatin; nephrotoxicity; malondialdehyde; pomegranate seed oil; total thiol content; OXIDATIVE STRESS; EXTRACT; KIDNEY; INHIBITION; METABOLISM; QUERCETIN; GROWTH; DAMAGE; DEATH; LIVER;
D O I
10.3109/0886022X.2015.1073496
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Clinical use of cisplatin is limited by its nephrotoxicity. Cisplatin-induced nephrotoxicity is associated with an increase in oxidative stress, leading ultimately to kidney dysfunction. The aim of this study was to investigate the effect of pomegranate seed oil against nephrotoxicity induced by cisplatin in adult rats. Methods: Animals were divided into four groups. Group I received corn oil (1 mL/kg). Group II received cisplatin (8 mg/kg). Group III and IV received pomegranate seed oil (PSO) 0.4 mL/kg and 0.8 mL/kg one hour before cisplatin injection for 3 days, respectively. Blood samples were collected by cardiac puncture and used for measuring urea and creatinine concentration. Twenty-hour urine samples were collected to measure protein and glucose concentration. The right kidney fixed in formalin for histological examination and the left kidney was homogenized for measurement of malondialdehyde and total sulfhydryl groups. Results: A significant elevation of serum creatinine, urea, urinary glucose, protein concentrations, and non-significant decrease in total thiol content and increase in MDA level in kidney homogenates were observed in cisplatin-treated rats. Also cisplatin reduced animal's body weight. Mild-to-moderate tubular cell necrosis, hyaline casts, and vascular congestion were observed in group II. PSO pre-treatment significantly decreased urinary protein, glucose, and serum creatinine concentration. PSO also caused a decrease in serum urea, renal MDA, and increase in thiol content, but the level of these parameters were not significant. Conclusion: The present results suggest that PSO is an effective agent for the prevention of cisplatin-induced renal dysfunction and oxidative damage in rat.
引用
收藏
页码:1338 / 1343
页数:6
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