Involvement of the Fas and Fas ligand in testicular germ cell apoptosis by zearalenone in rat

被引:26
作者
Jee, Youngheun [3 ]
Noh, Eun-Mi [1 ,2 ]
Cho, Eun-Sang [1 ,2 ]
Son, Hwa-Young [1 ,2 ]
机构
[1] Chungnam Natl Univ, Vet Med Res Inst, Taejon 305764, South Korea
[2] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[3] Jeju Natl Univ, Coll Vet Med, Cheju 690756, South Korea
关键词
apoptosis; estrogen receptor; Fas ligand; testis; zearalenone; ESTROGEN-RECEPTOR-ALPHA; MYCO-TOXIN; TESTES; MICE; SPERMATOGENESIS; EXPRESSION; EXPOSURE;
D O I
10.4142/jvs.2010.11.2.115
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Zearalenone (ZEA), a nonsteroidal estrogenic mycotoxin, is known to cause testicular toxicity in animals. In the present study, the effects of ZEA on spermatogenesis and possible mechanisms involved in germ cell injury were examined in rats. Ten-week-old Sprague-Dawley rats were treated with 5 mg/kg i.p. of ZEA and euthanized 3, 6, 12, 24 or 48 h after treatment. Histopathologically, spermatogonia and spermatocytes were found to be affected selectively. They were TUNEL-positive and found to be primarily in spermatogenic stages I-VI tubules from 6 h after dosing, increasing gradually until 12 h and then gradually decreasing. Western blot analysis revealed an increase in Fas and Fas ligand (Fas-L) protein levels in the ZEA-treated rats. However, the estrogen receptor (ER)alpha expression was not changed during the study. Collectively, our data suggest that acute exposure of ZEA induces apoptosis in germ cells of male rats and that this toxicity of ZEA is partially mediated through modulation of Fas and Fas-L systems, though ER alpha may not play a significant role.
引用
收藏
页码:115 / 119
页数:5
相关论文
共 27 条
[1]   Mycotoxins [J].
Bennett, JW ;
Klich, M .
CLINICAL MICROBIOLOGY REVIEWS, 2003, 16 (03) :497-+
[2]  
Biswas DK, 2005, SCI STKE, V288, ppe27
[3]  
Boekelheide K., 2005, J Natl cancer Inst Monogr, V34, P6, DOI DOI 10.1093/JNCIMONOGRAPHS/LGI006
[4]   Reduction of spermatogenesis in mice after tributyltin administration [J].
Chen, Yufang ;
Zuo, Zhenghong ;
Chen, Shuzhen ;
Yan, Feihuang ;
Chen, Yixin ;
Yang, Zengming ;
Wang, Chonggang .
TOXICOLOGY, 2008, 251 (1-3) :21-27
[5]   Effect of high intratesticular estrogen on the seminiferous epithelium in adult male rats [J].
D'Souza, R ;
Gill-Sharma, MK ;
Pathak, S ;
Kedia, N ;
Kumar, R ;
Balasinor, N .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2005, 241 (1-2) :41-48
[6]   Endogenous estrogens inhibit mouse fetal Leydig cell development via estrogen receptor α [J].
Delbès, G ;
Levacher, C ;
Duquenne, C ;
Racine, C ;
Pakarinen, P ;
Habert, R .
ENDOCRINOLOGY, 2005, 146 (05) :2454-2461
[7]   Elevated serum soluble Fas ligand is a promising marker of testicular toxicity induced by epirubicin in rats [J].
Geng, Jiang ;
Fan, Jie ;
Jiang, Hao-Wen ;
Fang, Zu-Jun ;
Wang, Xiang ;
Sun, Jian-Liang ;
Ding, Qiang ;
Chen, Gang .
TOXICOLOGY LETTERS, 2009, 186 (02) :96-103
[8]   ESTROGEN AND PROGESTERONE-RECEPTOR MESSENGER-RNA ARE EXPRESSED IN DISTINCT PATTERN IN MALE PRIMATE REPRODUCTIVE-ORGANS [J].
HEIKINHEIMO, O ;
MAHONY, MC ;
GORDON, K ;
HSIU, JG ;
HODGEN, GD ;
GIBBONS, WE .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 1995, 12 (03) :198-204
[9]  
Hikim APS, 1999, REV REPROD, V4, P38
[10]   Key apoptotic pathways for heat-induced programmed germ cell death in the testis [J].
Hikim, APS ;
Lue, YH ;
Yamamoto, CM ;
Vera, Y ;
Rodriguez, S ;
Yen, PH ;
Soeng, K ;
Wang, C ;
Swerdloff, RS .
ENDOCRINOLOGY, 2003, 144 (07) :3167-3175