首页> 美国卫生研究院文献>Toxicological Sciences >Dose Addition Models Based on Biologically Relevant Reductions in Fetal Testosterone Accurately Predict Postnatal Reproductive Tract Alterations by a Phthalate Mixture in Rats
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Dose Addition Models Based on Biologically Relevant Reductions in Fetal Testosterone Accurately Predict Postnatal Reproductive Tract Alterations by a Phthalate Mixture in Rats

机译:基于胎儿睾丸激素生物相关减少的剂量添加模型可准确预测大鼠邻苯二甲酸盐混合物对产后生殖道的影响

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摘要

Challenges in cumulative risk assessment of anti-androgenic phthalate mixtures include a lack of data on all the individual phthalates and difficulty determining the biological relevance of reduction in fetal testosterone (T) on postnatal development. The objectives of the current study were 2-fold: (1) to test whether a mixture model of dose addition based on the fetal T production data of individual phthalates would predict the effects of a 5 phthalate mixture on androgen-sensitive postnatal male reproductive tract development, and (2) to determine the biological relevance of the reductions in fetal T to induce abnormal postnatal reproductive tract development using data from the mixture study. We administered a dose range of the mixture (60, 40, 20, 10, and 5% of the top dose used in the previous fetal T production study consisting of 300 mg/kg per chemical of benzyl butyl (BBP), di(n)butyl (DBP), diethyl hexyl phthalate (DEHP), di-isobutyl phthalate (DiBP), and 100 mg dipentyl (DPP) phthalate/kg; the individual phthalates were present in equipotent doses based on their ability to reduce fetal T production) via gavage to Sprague Dawley rat dams on GD8-postnatal day 3. We compared observed mixture responses to predictions of dose addition based on the previously published potencies of the individual phthalates to reduce fetal T production relative to a reference chemical and published postnatal data for the reference chemical (called DAref). In addition, we predicted DA (called DAall) and response addition (RA) based on logistic regression analysis of all 5 individual phthalates when complete data were available. DA ref and DA all accurately predicted the observed mixture effect for 11 of 14 endpoints. Furthermore, reproductive tract malformations were seen in 17–100% of F1 males when fetal T production was reduced by about 25–72%, respectively.
机译:抗雄激素型邻苯二甲酸酯混合物的累积风险评估面临的挑战包括缺乏所有个体邻苯二甲酸酯的数据,以及难以确定胎儿睾丸激素(T)减少与产后发育的生物学相关性。当前研究的目标是2倍:(1)根据单个邻苯二甲酸盐的胎儿T产生数据测试添加剂量的混合模型是否可以预测5种邻苯二甲酸盐混合物对雄激素敏感的产后男性生殖道的影响(2)使用混合研究数据确定胎儿T降低以诱导异常的产后生殖道发育的​​生物学相关性。我们给予了该混合物的剂量范围(在先前的胎儿T生产研究中使用的最高剂量的60、40、20、10和5%),每种化合物的苄基丁基(BBP),二(n )(DBP),邻苯二甲酸二乙基己酯(DEHP),邻苯二甲酸二异丁酯(DiBP)和100 andmg邻苯二甲酸二戊酯(DPP)/ kg;根据减少胎儿T生成的能力,每种邻苯二甲酸盐的剂量均等。通过在出生后第3天第8天通过管饲法对Sprague Dawley大鼠大坝进行灌胃。我们根据先前公布的个别邻苯二甲酸酯相对于参考化学物质降低胎儿T产生的效力,比较了观察到的混合物对剂量增加的预测的混合物反应,并针对参考化学品(称为DAref)。此外,在获得完整数据时,我们基于对所有5种邻苯二甲酸酯的逻辑回归分析,预测了DA(称为DAall)和响应增加(RA)。 DA ref和DA都能准确预测14个端点中11个端点的混合效果。此外,当胎儿T生成量分别减少约25-72%时,在F-100男性中有17-100%的生殖道畸形。

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