Maternal di-(2-ethylhexyl) phthalate exposure during pregnancy causes fetal growth restriction in a stage-specific but gender-independent manner

被引:41
|
作者
Shen, Ru [1 ,2 ]
Zhao, Ling-Li [1 ,2 ]
Yu, Zhen [3 ]
Zhang, Cheng [1 ,2 ]
Chen, Yuan-Hua [1 ,2 ,4 ]
Wang, Hua [1 ,2 ]
Zhang, Zhi-Hui [1 ,2 ]
Xu, De-Xiang [1 ,2 ]
机构
[1] Anhui Med Univ, Dept Toxicol, Hefei, Peoples R China
[2] Anhui Med Univ, Lab Environm Toxicol, Hefei, Peoples R China
[3] Anhui Med Univ, Dept Maternal Child & Adolescent Hlth, Hefei, Peoples R China
[4] Anhui Med Univ, Dept Histol & Embryol, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
Di (2-ethylhexyl) phthalate (DEHP); Intrauterine growth restriction (IUGR); Developmental toxicity; Endocrine disrupting chemicals; N-BUTYL PHTHALATE; ENDOPLASMIC-RETICULUM STRESS; SEMEN QUALITY PARAMETERS; IN-UTERO EXPOSURE; MALE-RAT; REPRODUCTIVE HORMONES; TESTICULAR DYSGENESIS; PRENATAL EXPOSURE; TESTIS; MICE;
D O I
10.1016/j.reprotox.2016.12.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Di (2-ethylhexyl) phthalate (DEHP) is male developmental toxicant that impairs testis development with reduced anogenital distance. The present study aimed to investigate whether maternal DEHP exposure during pregnancy causes intrauterine growth restriction (IUGR) in a gender-specific manner and to identify the critical window of DEHP-induced fetal IUGR. Pregnant mice were administered with DEHP (0, 50 or 200 mg/kg) by gavage. Fetal IUGR was observed not only in males but also in females when litters were exposed to DEHP on gestational day (GD)0-GD17. Interestingly, fetal weight and crown-rump length were reduced, markedly in dams with DEHP on GD13-GD17, slightly in dams with on GD7-GD12, but not in dams with on GD0-GD6. Further analysis showed that maternal DEHP exposure on GD7-GD12 inhibited cell proliferation, lowered placental weight, and reduced blood sinusoid area in placental labyrinth layer. These results suggest that maternal DEHP exposure induces IUGR in a stage-specific but gender-independent manner. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:117 / 124
页数:8
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