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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >A mathematical approach to study combined effects of toxicants in vitro: evaluation of the Bliss independence criterion and the Loewe additivity model.
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A mathematical approach to study combined effects of toxicants in vitro: evaluation of the Bliss independence criterion and the Loewe additivity model.

机译:一种研究有毒物质在体外的综合作用的数学方法:Bliss独立性标准和Loewe可加性模型的评估。

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摘要

The study of interactions among toxicants is of fundamental interest and practical importance in toxicological sciences. However, a final agreement on the definition of agent interaction is lacking, and therefore, particular care should be adopted when using the terms additivity, synergism and antagonism, unless the exact toxicological pathways of the compounds studied are known. Two main different approaches, the Bliss independence criterion and the Loewe additivity model, have been generally used in co-exposure experiments. In some cases, they can present dramatically different results, depending on the slope of the pure dose-response curves of single substances. Here, we consider both models in in vitro experiments, where the dose-response curves can be extrapolated. Advantages and limitations of both approaches are discussed, using several mathematical simulations to better explain them, and applying the Hill function for the dose-response model curve. Overall we conclude that the Loewe additivity model is slightly preferable because of a general higher biological plausibility. However, which model to use must be determined case by case and the evaluation can be aided by experimental approaches, such as the study of multiple biomarkers and asynchronous exposures.
机译:对毒物之间相互作用的研究在毒理学中具有根本的兴趣和实际意义。但是,关于药物相互作用的定义尚缺乏最终协议,因此,除非已知所研究化合物的确切毒理学途径,否则在使用术语加和,协同作用和拮抗作用时应格外小心。共暴露实验通常使用两种主要的不同方法,即Bliss独立性准则和Loewe可加性模型。在某些情况下,它们可能会呈现出截然不同的结果,具体取决于单个物质的纯剂量反应曲线的斜率。在这里,我们在体外实验中都考虑了这两种模型,在这些模型中可以推断出剂量反应曲线。讨论了这两种方法的优点和局限性,使用几个数学模拟来更好地解释它们,并将Hill函数应用于剂量反应模型曲线。总的来说,我们得出的结论是,Loewe可加性模型由于普遍具有较高的生物似然性而略微可取。但是,必须根据具体情况确定使​​用哪种模型,并且可以通过实验方法(例如研究多种生物标志物和异步暴露)来辅助评估。

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