Pan Lianjun, Xia Xinyi, Feng Yao, Jiang Chunxia, Huang Yufeng
Department of Reproduction and Genetics, Nanjing University School of Clinical Medicine, Jinling Hospital, Nanjing, People's Republic of China.
Urology. 2007 Sep;70(3):613-7. doi: 10.1016/j.urology.2007.05.006.
To investigate the impact of exposure to the phytoestrogen daidzein on erectile function and sexual hormones. The negative effects of phytoestrogens on the male reproductive system, particularly on penile erection, have hardly been evaluated.
Thirty adult male Sprague-Dawley rats were equally divided into a normal control group, three experimental groups, and one positive control group. The three experimental groups were given daidzein at doses of 2, 20, and 100 mg/kg body weight daily, and the positive control group received 0.1 mg diethylstilbestrol per animal daily for 90 days. The apomorphine-induced erection test was performed 0, 30, 60, and 90 days after daidzein administration to evaluate for erectile function or dysfunction. After each test, blood samples were collected for plasma testosterone and luteinizing hormone measurement.
High-dose daidzein (100 mg/kg) decreased erectile responses to apomorphine from the 30th day of daidzein treatment and lasted to the 90th day without significant differences compared with the diethylstilbestrol-treated rats. However, similar changes were observed in the medium-dose daidzein (20 mg/kg) group from the 60th day. Low-dose daidzein (2 mg/kg) had no significant effect on the erectile responses to apomorphine compared with the normal control group (P >0.05). The plasma testosterone and luteinizing hormone levels showed a declining trend similar to that of the apomorphine-induced erections.
The phytoestrogen daidzein has the potential to adversely affect erectile function in a dose and time-related manner that is at least partly attributable to androgen deficiency. These findings implicate that phytoestrogens, especially isoflavones, if overconsumed for a long period, might be a novel risk factor for erectile dysfunction.
研究植物雌激素大豆苷元对勃起功能和性激素的影响。植物雌激素对男性生殖系统的负面影响,尤其是对阴茎勃起的影响,几乎未得到评估。
将30只成年雄性Sprague-Dawley大鼠平均分为正常对照组、三个实验组和一个阳性对照组。三个实验组每天分别给予2、20和100mg/kg体重的大豆苷元,阳性对照组每只动物每天给予0.1mg己烯雌酚,持续90天。在给予大豆苷元0、30、60和90天后进行阿扑吗啡诱导的勃起试验,以评估勃起功能或功能障碍。每次试验后,采集血样测定血浆睾酮和黄体生成素。
高剂量大豆苷元(100mg/kg)从大豆苷元治疗第30天起降低了对阿扑吗啡的勃起反应,并持续到第90天,与己烯雌酚治疗的大鼠相比无显著差异。然而,中剂量大豆苷元(20mg/kg)组从第60天起也观察到类似变化。低剂量大豆苷元(2mg/kg)与正常对照组相比,对阿扑吗啡诱导的勃起反应无显著影响(P>0.05)。血浆睾酮和黄体生成素水平呈现出与阿扑吗啡诱导勃起相似的下降趋势。
植物雌激素大豆苷元有可能以剂量和时间相关的方式对勃起功能产生不利影响,这至少部分归因于雄激素缺乏。这些发现表明,植物雌激素,尤其是异黄酮,如果长期过量摄入,可能是勃起功能障碍的一个新的危险因素。