Montelukast attenuates side effects of cisplatin including testicular, spermatological, and hormonal damage in male rats

被引:52
作者
Beytur, Ali [1 ]
Ciftci, Osman [2 ]
Oguz, Fatih [1 ]
Oguzturk, Hakan [3 ]
Yilmaz, Fethi [4 ]
机构
[1] Univ Inonu, Dept Urol, Fac Med, TR-44280 Malatya, Turkey
[2] Univ Inonu, Dept Pharmaceut Toxicol, Fac Pharm, TR-44280 Malatya, Turkey
[3] Univ Inonu, Dept Emergency Med, Fac Med, TR-44280 Malatya, Turkey
[4] Firat Univ, Elazig Sch Hlth Sci, TR-23119 Elazig, Turkey
关键词
Cisplatin; Montelukast; Reproductive toxicity; Testosterone; Oxidative damage; Sperm quality; MELATONIN; TOXICITY; INJURY; TESTIS; ASSAY;
D O I
10.1007/s00280-011-1692-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the current study, the protective effect of montelukast (ML) on cisplatin induced reproductive toxicity in rats was investigated. Twenty-eight rats were equally divided into four groups; first group was kept as control. In the second group, ML was orally administered at the dose of 10 mg/kg/day for 10 days. In the third group, CP was intraperitoneally administered at the dose of 7 mg/kg a single injection, and in fourth group, CP and ML were given together at the same doses. Although CP induced oxidative stress via significant increase in the formation of TBARS, it caused a significant decline in the levels of GSH, CAT, GPx, and SOD in rats. In contrast, ML prevents these effects of CP through cause an increase in GSH, CAT, GPx, and SOD levels and a decrease in formation of TBARS. In addition, sperm motility and serum testosterone levels significantly decrease and histopathological damage increases with CP treatment. However, the effects of CP on sperm motility, serum testosterone level, oxidative and histopathological changes are eliminated by ML treatment. In conclusion, the current study demonstrated that the reproductive toxicity caused by CP may be prevented by ML treatment. Thus, it was judged that co-administration of ML with CP may be useful to attenuate the negative effects of CP on male reproductive system.
引用
收藏
页码:207 / 213
页数:7
相关论文
共 31 条
[1]   The antioxidant activity of Vitamin C, DPPD and L-cysteine against Cisplatin-induced testicular oxidative damage in rats [J].
Ahmed, Emad A. ;
Omar, Hossam M. ;
Abd Elghaffar, Sary Kh ;
Ragb, Sohair M. M. ;
Nasser, Ahmed Y. .
FOOD AND CHEMICAL TOXICOLOGY, 2011, 49 (05) :1115-1121
[2]   Effects of Roselle and Ginger on cisplatin-induced reproductive toxicity in rats [J].
Amin, Amr ;
Hamza, AlaaEldin A. .
ASIAN JOURNAL OF ANDROLOGY, 2006, 8 (05) :607-612
[3]  
[Anonymous], 1974, Catalase. Methods Enzym. Anal., DOI DOI 10.1016/B978-0-12-091302-2.50032-3
[4]   Protective role of lycopene on cisplatin-induced changes in sperm characteristics, testicular damage and oxidative stress in rats [J].
Atessahin, A ;
Karahan, I ;
Türk, G ;
Gür, S ;
Yilmaz, S ;
Çeribasi, AO .
REPRODUCTIVE TOXICOLOGY, 2006, 21 (01) :42-47
[5]   Chemoprotective effect of melatonin against cisplatin-induced testicular toxicity in rats [J].
Atessahin, Ahmet ;
Sahna, Engin ;
Turk, Gaffari ;
Ceribasi, Ali Osman ;
Yilmaz, Seval ;
Yuce, Abdurrauf ;
Bulmus, Ozgur .
JOURNAL OF PINEAL RESEARCH, 2006, 41 (01) :21-27
[6]   Dual Inhibition of Wound Healing and Oxidative Process by Montelukast in Experimental Colon Anastomoses [J].
Canbay, Emel ;
Agachan, Bedia ;
Ozturk, Tulin ;
Giris, Murat ;
Asoglu, Oktar ;
Balik, Emre ;
Bugra, Dursun .
SURGICAL INNOVATION, 2010, 17 (03) :248-255
[7]  
Chainy GBN, 1997, ANDROLOGIA, V29, P343
[8]  
Ciftci O, 2010, HUM EXP TOXICOL, DOI [10.1177/096032711039006, DOI 10.1177/096032711039006]
[9]  
Ciftci O, 2011, ANDROLOGIA, DOI [10.1111/j.1439-0272.2010.01126, DOI 10.1111/J.1439-0272.2010.01126]
[10]  
Ciftci O, 2011, ANDROLOGIA, DOI [10.1111/j.1439-0272.2010.01127, DOI 10.1111/J.1439-0272.2010.01127]