کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5860968 | 1133273 | 2010 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
p,pâ²-DDE induces testicular apoptosis in prepubertal rats via the Fas/FasL pathway
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم محیط زیست
بهداشت، سم شناسی و جهش زایی
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چکیده انگلیسی
1,1-Dichloro-2,2 bis(p-chlorophenyl) ethylene (p,pâ²-DDE), the major metabolite of 2,2-bis(4-chlorophenyl)-1,1,1-trichloroethane (DDT), is a known persistent organic pollutant and male reproductive toxicant. It has antiandrogenic effect. However, the mechanism by which p,pâ²-DDE exposure causes male reproductive toxicity remains unknown. To elucidate the mechanism underpinning the testicular effects of p,pâ²-DDE, we sought to investigate Fas/FasL apoptotic pathway in the testis of prepubertal rats, including Fas, FasL, caspase-8, -3, and NF-κB. Animals were administered with different doses of p,pâ²-DDE (0, 20, 60, 100 mg/kg b.wt) every other day by intraperitoneal injection for 10 days. The results indicated that p,pâ²-DDE exposure at over 20 mg/kg b.wt showed the induction of apoptotic cell death. p,pâ²-DDE could induce increase in the MDA level, and decrease in SOD and GSH-Px activity. Significant elevations in the mRNA levels of Fas along with an increase in FasL, caspase-3, -8 were observed in 100 mg/kg b.wt group. In protein level, p,pâ²-DDE could induce increase of FasL and reduction of procaspase-8. NF-κB p65 was activated by p,pâ²-DDE treatment in rat testis. In addition, the activities of caspase-3, -8 were increased in 100 mg/kg b.wt group. Taken together, these results lead us to speculate that in vivo exposure to p,pâ²-DDE might induce testicular apoptosis in prepubertal rats through the Fas/FasL pathway.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology Letters - Volume 193, Issue 1, 1 March 2010, Pages 79-85
Journal: Toxicology Letters - Volume 193, Issue 1, 1 March 2010, Pages 79-85
نویسندگان
Yu-Qin Shi, Yu-Ping Wang, Yang Song, Hao-Wen Li, Chang-Jiang Liu, Zhi-Gang Wu, Ke-Di Yang,