Wang Wenxiang, Sun Yan, Liu Jin, Li Yuchen, Li Hong, Xiao Shihua, Weng Shaozheng, Zhang Wenchang
Department of Health Inspection and Quarantine, School of Public Health, Fujian Medical University, Fuzhou, Fujian, China; Fujian Province Key Laboratory of Environment and Health, School of Public Health, Fujian Medical University, Fuzhou, Fujian, China.
Center for Reproductive Medicine, Teaching Hospital of Fujian Medical University, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, China.
Food Chem Toxicol. 2014 Oct;72:51-60. doi: 10.1016/j.fct.2014.07.010. Epub 2014 Jul 14.
Twenty-one-day-old female Wistar rats were treated daily with orally administered soy isoflavones (SIFs) at concentrations of 50, 100, or 200 mg/kg body weight from weaning until sexual maturity (3 mo.), and ovarian follicle development was evaluated. At the end of the treatment period, the ultrastructure of the ovarian granulosa cells was examined by transmission electron microscopy. The apoptotic cell death of ovarian granulosa cells was detected using TUNEL staining. The mRNA expression levels of caspase-3, caspase-8, caspase-9, Bcl2, Bax, and Fas were determined by real-time quantitative PCR. The protein expression levels of caspase-3, Bcl2, Bax, and Fas were determined by western blotting. Our data showed that exposure to SIFs resulted in morphological changes consistent with ovarian granulosa cell apoptosis. The percentage of TUNEL-positive granulosa cells was increased. The mRNA expression levels of the apoptosis-related genes caspase-3, caspase-8, caspase-9, Bax, and Fas increased significantly. The protein levels of Bax, Fas, and cleaved caspase-3 were also increased. These results indicate that the exposure of rats to modest doses of SIFs from weaning until sexual maturity can affect ovarian follicle development by inducing apoptosis. The mechanism of SIF-induced alterations in ovarian follicle development may involve the activation of Fas-mediated and Bcl2/Bax-mediated apoptotic signaling pathways.
从断奶至性成熟(3个月)期间,每天给21日龄的雌性Wistar大鼠口服浓度为50、100或200mg/kg体重的大豆异黄酮(SIFs),并评估卵巢卵泡发育情况。在治疗期结束时,通过透射电子显微镜检查卵巢颗粒细胞的超微结构。使用TUNEL染色检测卵巢颗粒细胞的凋亡性细胞死亡。通过实时定量PCR测定caspase-3、caspase-8、caspase-9、Bcl2、Bax和Fas的mRNA表达水平。通过蛋白质印迹法测定caspase-3、Bcl2、Bax和Fas的蛋白质表达水平。我们的数据表明,暴露于SIFs会导致与卵巢颗粒细胞凋亡一致的形态学变化。TUNEL阳性颗粒细胞的百分比增加。凋亡相关基因caspase-3、caspase-8、caspase-9、Bax和Fas的mRNA表达水平显著增加。Bax、Fas和裂解的caspase-3的蛋白质水平也增加。这些结果表明,从断奶至性成熟期间,大鼠暴露于适度剂量的SIFs可通过诱导凋亡影响卵巢卵泡发育。SIF诱导卵巢卵泡发育改变的机制可能涉及Fas介导和Bcl2/Bax介导的凋亡信号通路的激活。