Zhang Linyuan, Dong Li, Ding Sijin, Qiao Peihuan, Wang Chong, Zhang Ming, Zhang Lixia, Du Qingcheng, Li Yimin, Tang Ning, Chang Bing
Key Laboratory of Chemical Safety and Health, National Institute for Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, No. 29 Nanwei Road, Xicheng District, Beijing 100050, China.
Institute for Environmental Health and Related Product Safety, Chinese Center for Disease Control and Prevention, No. 7 Panjiayuan Nanli, Chaoyang District, Beijing 100021, China.
Environ Toxicol Pharmacol. 2014 Mar;37(2):705-17. doi: 10.1016/j.etap.2014.01.016. Epub 2014 Feb 12.
Parabens are widely used as antibacterial agents, which are concerned recently in the relationship between the use of parabens and reproductive toxicity. So that reassessment of the risk of parabens is needed. In this study, one of parabens, n-butylparaben (n-BP) was orally administered to pregnant Wistar rats (0, 64, 160, 400 and 1000 mg/kg/day) from gestation day (GD) 7 through postnatal day (PND) 21. Reduced anogenital distance (AGD) and delayed preputial separation (PPS) were observed in the male offspring. The weights of the testes were significantly reduced at PND 21-90. The weights of the epididymides were significantly reduced at all monitoring points, except PND 35. Seminal vesicle weights were significantly reduced on PND 21. Serum testosterone (T) was significantly decreased, especially on PND 49. The levels of 17β-estradiol (E2) showed an increase at each of the tested points except on PND 180. Serum luteinising hormone (LH) and follicle-stimulating hormone (FSH) levels in the n-BP treated groups were lower on PND 21, 35 and 49 but elevated on PND 90 compared to control levels. n-BP reduced epididymal cauda sperm counts and daily sperm production in a dose-dependent manner; this difference was statistically significant at exposure groups of 400 and 1000 mg/kg/day. The present study strongly suggests that exposure to n-BP in utero and during lactation has adverse effects on the reproductive system in male offspring, with a no observed adverse effect level (NOAEL) of 160 mg/kg/day. To our knowledge, this is the first study that reports increased E2 levels of male rats following n-BP exposure; we suggest that E2 levels may be considered as biomarkers for some endocrine disrupting chemicals (EDCs).
对羟基苯甲酸酯被广泛用作抗菌剂,近来其使用与生殖毒性之间的关系受到关注。因此需要重新评估对羟基苯甲酸酯的风险。在本研究中,从妊娠第7天(GD)至出生后第21天(PND),将对羟基苯甲酸酯之一的对羟基苯甲酸正丁酯(n-BP)经口给予怀孕的Wistar大鼠(剂量分别为0、64、160、400和1000 mg/kg/天)。在雄性后代中观察到肛门生殖器距离(AGD)减小和包皮分离(PPS)延迟。在出生后第21至90天,睾丸重量显著降低。除出生后第35天外,在所有监测点附睾重量均显著降低。在出生后第21天,精囊重量显著降低。血清睾酮(T)显著降低,尤其是在出生后第49天。除出生后第180天外,在每个测试点17β-雌二醇(E2)水平均升高。与对照组相比,n-BP处理组在出生后第21、35和49天血清促黄体生成素(LH)和促卵泡生成素(FSH)水平较低,但在出生后第90天升高。n-BP以剂量依赖方式降低附睾尾部精子计数和每日精子生成量;在400和1000 mg/kg/天的暴露组中,这种差异具有统计学意义。本研究强烈表明,在子宫内和哺乳期暴露于n-BP对雄性后代的生殖系统有不良影响,未观察到不良影响水平(NOAEL)为160 mg/kg/天。据我们所知,这是第一项报道n-BP暴露后雄性大鼠E2水平升高的研究;我们建议E2水平可被视为某些内分泌干扰化学物质(EDC)的生物标志物。