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子宫内暴露于二苯甲酮-2会通过雌激素受体依赖性机制导致尿道下裂。

In utero exposure to benzophenone-2 causes hypospadias through an estrogen receptor dependent mechanism.

作者信息

Hsieh Michael H, Grantham Erin C, Liu Benchun, Macapagal Reginald, Willingham Emily, Baskin Laurence S

机构信息

Department of Urology, University of California-San Francisco, San Francisco, California, USA.

出版信息

J Urol. 2007 Oct;178(4 Pt 2):1637-42. doi: 10.1016/j.juro.2007.03.190. Epub 2007 Aug 16.

Abstract

PURPOSE

Additives such as benzophenone-2 are commonly used in cosmetic products and food container plastics to filter out ultraviolet light. In pregnant women exposure may result in transplacental transfer of benzophenone-2 to fetuses. Benzophenone-2 is estrogenic in vitro and in the rat uterotropic assay. Estradiol causes hypospadias in mice and estrogen-like compounds are also postulated to cause hypospadias. We determined whether hypospadias would develop in male mice exposed to benzophenone-2 in utero and whether this outcome depended on estrogen receptor pathways.

MATERIALS AND METHODS

Timed pregnant C57BL/6 mice were administered benzophenone-2 (6.25 mg) or control vehicle by oral gavage from gestational days 12 through 17 and they were sacrificed on day 18. Fetuses were weighed and sexed, anogenital distance was measured and genital tubercles were harvested for paraffin sections or quantitative reverse transcriptase-polymerase chain reaction analysis of genes purportedly involved in genital tubercle development.

RESULTS

Eight of 57 benzophenone-2 treated male fetuses (14%) whose genital tubercles were examined histologically had hypospadias (p = 0.0064). Co-administration of benzophenone-2 with the estrogen receptor antagonist EM-800 resulted in normal genital tubercles, ie no hypospadias, in 26 of 26 mice. Likewise no EM-800 or control treated male genital tubercles showed hypospadias. Benzophenone-2 treated male mice had no changes in body mass adjusted anogenital distance relative to controls. Reverse transcriptase-polymerase chain reaction revealed that genital tubercles of benzophenone-2 treated male mice expressed higher levels of estrogen receptor-beta relative to male controls (p = 0.04).

CONCLUSIONS

These findings suggest that benzophenone-2 may cause hypospadias via signaling through the estrogen receptor. Further study of human benzophenone-2 exposure and its effects is needed to support this hypothesis.

摘要

目的

二苯甲酮 - 2等添加剂常用于化妆品和食品包装塑料中,以过滤紫外线。孕妇接触二苯甲酮 - 2可能导致其经胎盘转移至胎儿体内。二苯甲酮 - 2在体外和大鼠子宫增重试验中具有雌激素活性。雌二醇会导致小鼠尿道下裂,也有推测认为雌激素样化合物会导致尿道下裂。我们确定了子宫内暴露于二苯甲酮 - 2的雄性小鼠是否会发生尿道下裂,以及这一结果是否依赖于雌激素受体途径。

材料与方法

对处于特定孕期的C57BL/6小鼠从妊娠第12天至第17天经口灌胃给予二苯甲酮 - 2(6.25毫克)或对照载体,于第18天处死。对胎儿进行称重和性别鉴定,测量肛门与生殖器间距离,并采集生殖器结节用于石蜡切片或对据推测参与生殖器结节发育的基因进行定量逆转录聚合酶链反应分析。

结果

在57只经组织学检查生殖器结节的二苯甲酮 - 2处理雄性胎儿中,有8只(14%)出现尿道下裂(p = 0.0064)。二苯甲酮 - 2与雌激素受体拮抗剂EM - 800共同给药后,26只小鼠中有26只生殖器结节正常,即未出现尿道下裂。同样,未接受EM - 800或对照处理的雄性生殖器结节也未出现尿道下裂。与对照组相比,二苯甲酮 - 2处理的雄性小鼠经体重调整后的肛门与生殖器间距离无变化。逆转录聚合酶链反应显示,二苯甲酮 - 2处理的雄性小鼠生殖器结节中雌激素受体β的表达水平相对于雄性对照组更高(p = 0.04)。

结论

这些发现表明,二苯甲酮 - 2可能通过雌激素受体信号传导导致尿道下裂。需要进一步研究人类接触二苯甲酮 - 2及其影响,以支持这一假设。

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