Wilson Vickie S, Lambright Christy R, Furr Johnathan R, Howdeshell Kembra L, Earl Gray L
U.S. Environmental Protection Agency, Office of Research and Development, NHEERL, Research Triangle Park, NC, USA.
Toxicol Lett. 2009 Apr 25;186(2):73-7. doi: 10.1016/j.toxlet.2008.12.017. Epub 2009 Jan 9.
In utero exposure to linuron, an urea-based herbicide, results in a pattern of malformations of androgen-dependent tissues in adult male rat offspring resembling that produced by some phthalate esters which are known to decrease fetal testosterone production. This study investigated the impact of in utero linuron treatment on fetal testis gene expression and testosterone production. Timed-pregnant Sprague Dawley rats were administered corn oil vehicle, 12.5, 25, 50 or 75mg linuron/day/kg orally from GD13 to 18. Ex vivo testosterone (T) production was significantly decreased at 50 and 75mg/kg when analyzed on a per litter basis. Unlike the phthalate esters, linuron treatment did not affect insl3, cyp17a, cyp11a or StAR mRNA expression. Control GD18 fetal testes were then incubated with increasing concentrations of linuron (1-300microM) to evaluate if linuron inhibited T production in vitro. T production was significantly reduced at 30microM and above. Progesterone production was not affected in any of the studies indicating that linuron directly inhibited testosterone production in the absence of cytotoxicity. These results indicate the malformations induced by linuron and phthalate esters in male offspring are similar because both reduce fetal T levels during the critical period of sex differentiation but suggest that the mechanisms differ.
子宫内暴露于利谷隆(一种基于尿素的除草剂)会导致成年雄性大鼠后代雄激素依赖组织出现畸形模式,类似于某些已知会降低胎儿睾酮生成的邻苯二甲酸酯所产生的畸形模式。本研究调查了子宫内利谷隆处理对胎儿睾丸基因表达和睾酮生成的影响。将定时怀孕的斯普拉格 - 道利大鼠从妊娠第13天至第18天每天按12.5、25、50或75毫克利谷隆/千克体重口服给予玉米油载体。按每窝分析时,50和75毫克/千克剂量下的体外睾酮(T)生成显著降低。与邻苯二甲酸酯不同,利谷隆处理不影响胰岛素样肽3(Insl3)、细胞色素P450 17α(Cyp17a)、细胞色素P450 11α(Cyp11a)或类固醇生成急性调节蛋白(StAR)的mRNA表达。然后将对照的妊娠第18天胎儿睾丸与浓度不断增加的利谷隆(1 - 300微摩尔)一起孵育,以评估利谷隆在体外是否抑制睾酮生成。30微摩尔及以上浓度时睾酮生成显著降低。在任何研究中孕酮生成均未受影响,这表明利谷隆在无细胞毒性的情况下直接抑制睾酮生成。这些结果表明,利谷隆和邻苯二甲酸酯在雄性后代中诱导的畸形相似,因为两者在性别分化的关键时期均降低胎儿T水平,但提示其机制不同。