Deglucosylation of zearalenone-14-glucoside in animals and human liver leads to underestimation of exposure to zearalenone in humans
文献类型: 外文期刊
第一作者: Yang, Shupeng
作者: Yang, Shupeng;Zhang, Jinzhen;Jin, Yue;Li, Yi;Zhou, Jinhui;Sun, Feifei;Yang, Shupeng;Zhang, Huiyan;De Saeger, Sarah;De Boevre, Marthe;Yang, Shupeng;Zhang, Huiyan;Zhang, Suxia;Sun, Feifei;Li, Yanshen
作者机构:
关键词: Zearalenone; Zearalenone-14-glucoside; Metabolism; Modified mycotoxin
期刊名称:ARCHIVES OF TOXICOLOGY ( 影响因子:5.153; 五年影响因子:6.352 )
ISSN: 0340-5761
年卷期: 2018 年 92 卷 9 期
页码:
收录情况: SCI
摘要: Zearalenone-14-glucoside (ZEN-14G), the modified mycotoxin of zearalenone (ZEN), has attracted considerable attention due to its high potential to be hydrolyzed into ZEN, which would exert toxicity. It has been confirmed that the microflora could metabolize ZEN-14G to ZEN. However, the metabolic profile of ZEN-14G and whether it could be deglucosidated in the liver are unknown. To thoroughly investigate the metabolism of ZEN-14G, in vitro metabolism including phase I and phase II metabolism was studied using liquid chromatography coupled to high-resolution mass spectrometry. Additionally, in vivo metabolism of ZEN-14G was conducted in model animals, rats, by oral administration. As a result, 29 phase I metabolites and 6 phase II metabolites were identified and significant inter-species metabolic differences were observed as well. What is more, ZEN-14G could be considerably deglucosidated into its free form of ZEN after the incubation with animals and human liver microsomes in the absence of NADPH, which was mainly metabolized by human carboxylesterase CES-I and II. Furthermore, results showed that the major metabolic pathways of ZEN-14G were deglucosylation, hydroxylation, hydrogenation and glucuronidation. Although interspecies differences in the biotransformation of ZEN-14G were observed, ZEN, alpha-ZEL-14G, beta-ZEL-14G, alpha-ZEL, ZEN-14G-16GlcA and ZEN-14GlcA were the major metabolites of ZEN-14G. Additionally, a larger yield of 6-OH-ZEN-14G and 8-OH-ZEN-14G was also observed in human liver microsomes. The obtained data would be of great importance for the safety assessment of modified mycotoxin, ZEN-14G, and provide another perspective for risk assessment of mycotoxin.
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