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食物源烯基苯并呋喃型化合物黄樟素和沙菲醇联合暴露的体外和计算研究。

In vitro and in silico study on consequences of combined exposure to the food-borne alkenylbenzenes estragole and safrole.

机构信息

Division of Toxicology, Wageningen University, Stippeneng 4, 6708 WE Wageningen, the Netherlands.

Division of Toxicology, Wageningen University, Stippeneng 4, 6708 WE Wageningen, the Netherlands.

出版信息

Toxicol In Vitro. 2022 Mar;79:105290. doi: 10.1016/j.tiv.2021.105290. Epub 2021 Nov 30.

Abstract

Potential consequences of combined exposure to the selected food-borne alkenylbenzenes safrole and estragole or their proximate carcinogenic 1'-hydroxy metabolites were evaluated in vitro and in silico. HepG2 cells were exposed to 1'-hydroxyestragole and 1'-hydroxysafrole individually or in equipotent combination subsequently detecting cytotoxicity and DNA adduct formation. Results indicate that concentration addition adequately describes the cytotoxic effects and no statistically significant differences were shown in the level of formation of the major DNA adducts. Furthermore, physiologically based kinetic modeling revealed that at normal dietary intake the concentration of the parent compounds and their 1'-hydroxymetabolites remain substantially below the Km values for the respective bioactivation and detoxification reactions providing further support for the fact that the simultaneous presence of the two carcinogens or of their proximate carcinogenic 1'-hydroxy metabolites may not affect their DNA adduct formation. Overall, these results point at the absence of interactions upon combined exposure to selected food-borne alkenylbenzenes at realistic dietary levels of intake.

摘要

潜在的联合暴露于选定的食物源烯基苯并呋喃(如黄樟素和欧芹酚)或其近似致癌 1'-羟基代谢物的后果,通过体外和计算机模拟进行了评估。将 HepG2 细胞分别暴露于 1'-羟基欧芹酚和 1'-羟基黄樟素,或暴露于等效力的混合物中,随后检测细胞毒性和 DNA 加合物形成。结果表明,浓度加和法充分描述了细胞毒性效应,并且在主要 DNA 加合物形成水平上没有显示出统计学上的显著差异。此外,基于生理学的动力学建模表明,在正常饮食摄入的情况下,母体化合物及其 1'-羟基代谢物的浓度仍远低于各自生物活化和解毒反应的 Km 值,这进一步支持了这样一个事实,即两种致癌物质或其近似致癌的 1'-羟基代谢物同时存在可能不会影响它们的 DNA 加合物形成。总体而言,这些结果表明,在摄入实际饮食水平的情况下,联合暴露于选定的食物源烯基苯并呋喃时,不存在相互作用。

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