Effects of In Utero Exposure to Di-n-Butyl Phthalate on Testicular Development in Rat

被引:31
作者
Ma, Tan [1 ,2 ,3 ]
Yin, Xiaoqin [1 ,2 ,3 ]
Han, Ruitong [1 ,2 ,3 ]
Ding, Jie [1 ,2 ,3 ]
Zhang, Huan [4 ]
Han, Xiaodong [1 ,2 ,3 ]
Li, Dongmei [1 ,2 ,3 ]
机构
[1] Nanjing Univ, Med Sch, Immunol & Reprod Biol Lab, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Med Sch, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Jiangsu Key Lab Mol Med, Nanjing 210093, Jiangsu, Peoples R China
[4] Linkoping Univ, Dept Clin & Expt Med, SE-58183 Linkoping, Sweden
来源
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH | 2017年 / 14卷 / 10期
基金
中国国家自然科学基金;
关键词
prenatal DBP exposure; testicular cells; ras related dexamethasone induced 1 (Rasd1); MEK1/2; Bcl-2; Bax; cell proliferation; apoptosis; MALE REPRODUCTIVE DEVELOPMENT; DI(N-BUTYL) PHTHALATE; DIBUTYL PHTHALATE; DYSGENESIS SYNDROME; PROGRAMMING WINDOW; SERTOLI-CELLS; FETAL TESTIS; TRACT; PROLIFERATION; DISRUPTION;
D O I
10.3390/ijerph14101284
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Humans are inevitably exposed to ubiquitous phthalate esters (PAEs). In utero exposure to di-n-butyl phthalate (DBP) induces abnormal development of the testis and reproductive tract in male offspring, which correspond closely with the human condition of testicular dysgenesis syndrome (TDS)-like syndrome. However, the underlying mechanisms have not been elucidated in detail. In this study, pregnant rats were orally exposed to either corn oil (controls) or DBP at three different doses by gavage during Gestational Days 12.5-21.5. Pathological examinations were performed for toxicity evaluation. Proliferation and apoptosis related proteins (ras related dexamethasone induced 1 (Rasd1), mitogen-activated protein kinase kinases1/2 (MEK1/2), Bcl-2, and Bax) were measured for mechanisms exploration. The results showed that different doses of DBP caused male developmental and reproductive toxicity in rats, including the decrease of anogenital distance (AGD), the histological damage of testis, and apoptosis of seminiferous tubule cells. Our data suggested that DBP played chronic and continuous toxic roles on male reproductive system by disrupting expression of Rasd1 and MEK1/2 as well as Bcl-2/Bax ratio. Further research is warranted.
引用
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页数:12
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