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一种用于量化玉米赤霉烯酮肠道微生物生物活化和解毒动力学种间差异的模型。

An model to quantify interspecies differences in kinetics for intestinal microbial bioactivation and detoxification of zearalenone.

作者信息

Mendez-Catala Diana M, Spenkelink Albertus, Rietjens Ivonne M C M, Beekmann Karsten

机构信息

Division of Toxicology, Wageningen University and Research, the Netherlands.

出版信息

Toxicol Rep. 2020 Jul 24;7:938-946. doi: 10.1016/j.toxrep.2020.07.010. eCollection 2020.

Abstract

Zearalenone (ZEN) is a mycotoxin known for its estrogenic activities. The metabolism of ZEN plays a role in the interspecies differences in sensitivity to ZEN, and is known to occur in the liver and the intestinal microbiota, although the relative contribution of these two pathways remains to be characterized. In the present study a fecal model was optimized and used to quantify the interspecies differences in kinetics of the intestinal microbial metabolism of ZEN in rat, pig and human. V, K, and catalytic efficiencies (k) were determined, and results obtained reveal that the k values for formation of α-ZEL and β-ZEL amounted to 0.73 and 0.12 mL/h/kg bw for human microbiota, 2.6 and 1.3 mL/h/kg bw for rat microbiota and 9.4 and 6.3 mL/h/kg bw for pig microbiota showing that overall ZEN metabolism increased in the order human < rat < pig microbiota. Expressed per kg bw the k for ZEN metabolism by the liver surpassed that of the intestinal microbiota in all three species. In conclusion, it is estimated that the activity of the intestinal colon microbiome may be up to 36 % of the activity of the liver, and that it can additionally contribute to the species differences in bioactivation and detoxification and thus the toxicity of ZEN in pigs and rats but not in humans. The results highlight the importance of the development of human specific models for the assessment of the metabolism of ZEN.

摘要

玉米赤霉烯酮(ZEN)是一种以其雌激素活性而闻名的霉菌毒素。ZEN的代谢在对ZEN敏感性的种间差异中起作用,已知其在肝脏和肠道微生物群中发生,尽管这两种途径的相对贡献仍有待确定。在本研究中,优化了一种粪便模型,并用于量化大鼠、猪和人类肠道微生物对ZEN代谢动力学的种间差异。测定了V、K和催化效率(k),所得结果表明,人类微生物群形成α-ZEL和β-ZEL的k值分别为0.73和0.12 mL/h/kg体重,大鼠微生物群为2.6和1.3 mL/h/kg体重,猪微生物群为9.4和6.3 mL/h/kg体重,表明总体上ZEN代谢按人类<大鼠<猪微生物群的顺序增加。按每千克体重计算,所有三个物种中肝脏对ZEN代谢的k值均超过肠道微生物群。总之,据估计,肠道结肠微生物群的活性可能高达肝脏活性的36%,并且它可以额外导致生物激活和解毒的种间差异,从而导致ZEN在猪和大鼠而非人类中的毒性。结果突出了开发用于评估ZEN代谢的人类特异性模型的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0d/7406981/5828e3b79f7b/ga1.jpg

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