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首页> 外文期刊>Archives of Toxicology >Use of an in vitro-in silico testing strategy to predict inter-species and inter-ethnic human differences in liver toxicity of the pyrrolizidine alkaloids lasiocarpine and riddelliine
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Use of an in vitro-in silico testing strategy to predict inter-species and inter-ethnic human differences in liver toxicity of the pyrrolizidine alkaloids lasiocarpine and riddelliine

机译:使用体外硅测试策略来预测吡咯烷生物碱肝毒性肝脏毒性和脱霉菌的肝脏毒性的种类和族裔人群差异

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Lasiocarpine and riddelliine are pyrrolizidine alkaloids (PAs) known to cause liver toxicity. The aim of this study was to predict the inter-species and inter-ethnic human differences in acute liver toxicity of lasiocarpine and riddelliine using physiologically based kinetic (PBK) modelling based reverse dosimetry of in vitro toxicity data. The concentration-response curves of in vitro cytotoxicity of lasiocarpine and riddelliine defined in pooled human hepatocytes were translated to in vivo dose-response curves by PBK models developed using kinetic data obtained from incubations with pooled tissue fractions from Chinese and Caucasian individuals, providing PBK models for the average Chinese and average Caucasian, respectively. From the predicted in vivo dose-response curves, the benchmark dose lower and upper confidence limits for 5% effect (BMDL5 and BMDU5) were derived and subsequently compared to those previously obtained in rat to evaluate inter-species differences. The inter-species differences amounted to 2.0-fold for lasiocarpine and 8.2-fold for riddelliine with humans being more sensitive than rats. The inter-ethnic human differences varied 2.0-fold for lasiocarpine and 5.0-fold for riddelliine with the average Caucasian being more sensitive than the average Chinese. In conclusion, the present study provides the proof-of-principle to predict inter-species and inter-ethnic differences in in vivo liver toxicity for PAs by an alternative testing strategy integrating in vitro cytotoxicity data with PBK modelling-based reverse dosimetry.
机译:Lasiocarpine和Riddelliine是已知引起肝脏毒性的吡咯烷类生物碱(PAS)。本研究的目的是使用基于体外毒性数据的逆向剂量的基于生理基础的动力学(PBK)建模,预测Lasiocarpine和Riddelliine的急性肝毒性的急性肝毒性的种类间和族间的人群差异。通过使用从中国和白种人个人的合并组织分数所获得的动力学数据,通过与来自中华人民主人个人的合并组织部分产生的动力学数据开发的PBK模型转化为体内剂量 - 响应曲线的升高的人肝细胞和RADDelliine的浓度 - 反应曲线。提供PBK模型对于普通人和平均白种人来说。从预测的体内剂量 - 响应曲线中,衍生5%效应(BMDL5和BMDU5)的基准剂量降低和上置信限制,并随后与预先在大鼠中获得的那些进行评估,评估物种间差异。对于Lasiocarpine的物种间差异为2.0倍,并且对于人类比大鼠更敏感的人类的riddelliine为8.2倍。 Lasiocarpine的民族间的人类差异不同2.0倍,riddelliine为5.0倍,平均白种人比普通汉语更敏感。总之,本研究提供了原则上,通过将体外细胞毒性数据与基于PBK建模的反向剂量分别相结合的替代测试策略来预测PAS的种类群体和种族间差异。

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