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真菌毒素:利用 Caco-2 细胞单层进行生物转化和生物利用度评估。

Mycotoxins: Biotransformation and Bioavailability Assessment Using Caco-2 Cell Monolayer.

机构信息

Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technicka 3, 166 28 Prague 6, Czech Republic.

出版信息

Toxins (Basel). 2020 Sep 30;12(10):628. doi: 10.3390/toxins12100628.

Abstract

The determination of mycotoxins content in food is not sufficient for the prediction of their potential in vivo cytotoxicity because it does not reflect their bioavailability and mutual interactions within complex matrices, which may significantly alter the toxic effects. Moreover, many mycotoxins undergo biotransformation and metabolization during the intestinal absorption process. Biotransformation is predominantly the conversion of mycotoxins meditated by cytochrome P450 and other enzymes. This should transform the toxins to nontoxic metabolites but it may possibly result in unexpectedly high toxicity. Therefore, the verification of biotransformation and bioavailability provides valuable information to correctly interpret occurrence data and biomonitoring results. Among all of the methods available, the in vitro models using monolayer formed by epithelial cells from the human colon (Caco-2 cell) have been extensively used for evaluating the permeability, bioavailability, intestinal transport, and metabolism of toxic and biologically active compounds. Here, the strengths and limitations of both in vivo and in vitro techniques used to determine bioavailability are reviewed, along with current detailed data about biotransformation of mycotoxins. Furthermore, the molecular mechanism of mycotoxin effects is also discussed regarding the disorder of intestinal barrier integrity induced by mycotoxins.

摘要

食品中霉菌毒素含量的测定不足以预测其在体内的潜在细胞毒性,因为它不能反映其生物利用度和在复杂基质中的相互作用,而这些因素可能会显著改变其毒性作用。此外,许多霉菌毒素在肠道吸收过程中会发生生物转化和代谢。生物转化主要是由细胞色素 P450 和其他酶介导的霉菌毒素转化。这应该将毒素转化为无毒代谢物,但也可能导致意外的高毒性。因此,生物转化和生物利用度的验证为正确解释发生数据和生物监测结果提供了有价值的信息。在所有可用的方法中,使用源自人结肠的上皮细胞形成的单层(Caco-2 细胞)的体外模型已被广泛用于评估毒性和生物活性化合物的通透性、生物利用度、肠道转运和代谢。本文综述了用于确定生物利用度的体内和体外技术的优缺点,并详细介绍了霉菌毒素生物转化的最新数据。此外,还讨论了霉菌毒素对肠道屏障完整性紊乱的影响,以及霉菌毒素对肠道屏障完整性紊乱的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6be4/7601793/846cb2167276/toxins-12-00628-g001.jpg

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