Department of Pharmacy, School of Pharmacy of Wenzhou Medical University, Chashan District, Wenzhou 325000, Zhejiang, China.
Research Academy of Reproductive Biomedicine, the 2nd Affiliated Hospital, Wenzhou Medical University, Wenzhou 325027, Zhejiang, China.
Int J Mol Sci. 2014 May 6;15(5):7812-26. doi: 10.3390/ijms15057812.
The objective of the present study is to determine whether methoxychlor (MXC) exposure in adulthood affects rat Leydig cell regeneration and to compare its effects with estradiol (E2). Adult 90-day-old male Sprague-Dawley rats received ethane dimethane sulfonate (EDS) to eliminate the adult Leydig cell population. Subsequently, rats were randomly assigned to four groups and gavaged with corn oil (control), 0.25 mg/kg E2 and 10 or 100 mg/kg MXC daily from days 5 to 30 post-EDS treatment. The results showed that MXC and E2 reduced serum testosterone levels on day 58 post-EDS treatment. qPCR showed Hsd17b3 mRNA levels were downregulated 7-15 fold by E2 and MXC, indicating that development of the new population of Leydig cells was arrested at the earlier stage. This observation was supported by the results of histochemical staining, which demonstrated that Leydig cells in MXC-treated testis on day 58 post-EDS treatment were mostly progenitor Leydig cells. However, Pdgfb mRNA levels were downregulated, while Lif transcript levels were increased by MXC. In contrast, E2 did not affect gene expression for these growth factors. In conclusion, our findings indicated that both MXC and E2 delayed rat Leydig cell regeneration in the EDS-treated model, presumably acting by different mechanisms.
本研究旨在确定成年期甲氧滴滴涕(MXC)暴露是否会影响大鼠睾丸间质细胞的再生,并比较其与雌二醇(E2)的影响。成年 90 日龄雄性 Sprague-Dawley 大鼠接受乙烷二甲磺酸酯(EDS)处理以消除成年睾丸间质细胞群体。随后,大鼠被随机分配到四组,从 EDS 处理后第 5 天至第 30 天每天灌胃玉米油(对照)、0.25mg/kg E2 和 10 或 100mg/kg MXC。结果表明,MXC 和 E2 在 EDS 处理后第 58 天降低了血清睾酮水平。qPCR 显示 Hsd17b3 mRNA 水平被 E2 和 MXC 下调 7-15 倍,表明新的睾丸间质细胞群体的发育在早期阶段被阻断。组织化学染色的结果支持了这一观察结果,显示 EDS 处理后第 58 天 MXC 处理的睾丸中的睾丸间质细胞大多是祖细胞睾丸间质细胞。然而,MXC 下调了 Pdgfb mRNA 水平,而 Lif 转录物水平增加。相比之下,E2 对这些生长因子的基因表达没有影响。总之,我们的研究结果表明,MXC 和 E2 都延迟了 EDS 处理模型中大鼠睾丸间质细胞的再生,可能通过不同的机制起作用。