Two-hit exposure to polychlorinated biphenyls at gestational and juvenile life stages: 2. Sex-specific neuromolecular effects in the brain

被引:25
作者
Bell, Margaret R. [1 ]
Hart, Bethany G. [1 ]
Gore, Andrea C. [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Pharmacol & Toxicol, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Neurosci, Austin, TX 78712 USA
关键词
Endocrine-disrupting chemical; Preoptic area; Dopamine receptor; Mu opioid receptor; Androgen receptor; Estrogen receptor; SEXUALLY DIMORPHIC NUCLEUS; MEDIAL PREFRONTAL CORTEX; ANXIETY-RELATED BEHAVIOR; ESTROGEN-RECEPTOR-ALPHA; NONHUMAN PRIMATE BRAIN; ADULT SOCIAL-BEHAVIOR; DNA METHYLATION; PCB CONGENERS; PREOPTIC AREA; MALE-RATS;
D O I
10.1016/j.mce.2015.11.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Exposures to polychlorinated biphenyls (PCBs) during early development have long-lasting, sexually dimorphic consequences on adult brain and behavior. However, few studies have investigated their effects during juvenile development, a time when increases in pubertal hormones influence brain maturation. Here, male and female Sprague Dawley rats were exposed to PCBs (Aroclor 1221, 1 mg/kg/day) or vehicle prenatally, during juvenile development, or both, and their effects on serum hormone concentrations, gene expression, and DNA methylation were assessed in adulthood. Gene expression in male but not female brains was affected by 2-hits of PCBs, a result that paralleled behavioral effects of PCBs. Furthermore, the second hit often changed the effects of a first hit in complex ways. Thus, PCB exposures during critical fetal and juvenile developmental periods result in unique neuromolecular phenotypes, with males most vulnerable to the treatments. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:125 / 137
页数:13
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