Rashad Maha M, Galal Mona K, El-Behairy Adel M, Gouda Eman M, Moussa Said Z
1 Biochemistry Department, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Toxicol Ind Health. 2018 Nov;34(11):744-752. doi: 10.1177/0748233718791623. Epub 2018 Sep 19.
The aim of this study was to investigate the effects of maternal exposure to di-( n-butyl) phthalate (DBP) on testicular development and function in pre-pubertal and post-pubertal male rat offspring. Fourteen pregnant female rats were equally divided into two groups: a control group and a DBP-treated group. During gestation day (GD) 12 to postnatal day (PND) 14, the control group was administered 1 ml/day corn oil, and the DBP-treated group was administered DBP 500 mg/kg/day by oral gavage. On PND 25 (pre-puberty) and PND 60 (post-puberty), blood for serum and the testes were collected from five male offspring of each group. To determine the relationship between the methylation state of the c-Myc promoter and the expression of the c-Myc gene, some apoptotic-related genes, such as p53 and Bax, the anti-apoptotic Bcl-2 gene, and some growth arrest-related genes, such as BRD7 and GAS1, were examined. Compared with the control ( p < 0.05), at pre-puberty, DBP induces c-Myc hyper-methylation with significant downregulation for c-Myc, p53, Bax genes, and significant upregulation for Bcl-2, BRD7, and GAS1, while at post puberty, the methylation state and expression of c-Myc and apoptosis-related genes returned to control levels in the same sequence with the fold change in the expression of BRD7 and GAS1 genes. These findings suggest that DBP induced a transient pre-pubertal increase in c-Myc promoter methylation that may be associated with disruption of both apoptotic and growth mechanisms in the testes.
本研究旨在探讨母体暴露于邻苯二甲酸二(正丁基)酯(DBP)对青春期前和青春期后雄性大鼠子代睾丸发育和功能的影响。将14只怀孕的雌性大鼠平均分为两组:对照组和DBP处理组。在妊娠第12天(GD)至出生后第14天(PND)期间,对照组每天给予1毫升玉米油,DBP处理组通过灌胃给予500毫克/千克/天的DBP。在出生后第25天(青春期前)和第60天(青春期后),从每组的5只雄性子代中采集血清和睾丸样本。为了确定c-Myc启动子的甲基化状态与c-Myc基因表达之间的关系,检测了一些凋亡相关基因,如p53和Bax、抗凋亡Bcl-2基因,以及一些生长停滞相关基因,如BRD7和GAS1。与对照组相比(p<0.05),在青春期前,DBP诱导c-Myc高度甲基化,c-Myc、p53、Bax基因显著下调,Bcl-2、BRD7和GAS1基因显著上调;而在青春期后,c-Myc的甲基化状态和表达以及凋亡相关基因按相同顺序恢复到对照水平,BRD7和GAS1基因表达的变化倍数与之相同。这些发现表明,DBP诱导青春期前c-Myc启动子甲基化短暂增加,这可能与睾丸凋亡和生长机制的破坏有关。