Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats

Bioaccumulation and biotransformation are critical factors that affect the release of easily metabolizable chemicals to cause human toxicity. The glucoside-type modified mycotoxin Zearalenone-14-Glucoside (Z14G) has attracted global attention for its high occurrence in foodstuffs and the potential t...

Full description

Bibliographic Details
Main Authors: Qian Lu, Ming Sui, Ya-Wen Luo, Jiao-Yang Luo, Mei-Hua Yang
Format: Article
Language:English
Published: Elsevier 2022-11-01
Series:Ecotoxicology and Environmental Safety
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0147651322010247
_version_ 1828730222533410816
author Qian Lu
Ming Sui
Ya-Wen Luo
Jiao-Yang Luo
Mei-Hua Yang
author_facet Qian Lu
Ming Sui
Ya-Wen Luo
Jiao-Yang Luo
Mei-Hua Yang
author_sort Qian Lu
collection DOAJ
description Bioaccumulation and biotransformation are critical factors that affect the release of easily metabolizable chemicals to cause human toxicity. The glucoside-type modified mycotoxin Zearalenone-14-Glucoside (Z14G) has attracted global attention for its high occurrence in foodstuffs and the potential threat to humans as its high rate of transformation into parent forms. Given the limited toxicokinetics information, this study assessed the absorption, distribution, biotransformation and excretion of Z14G, aiming to define the potential risk of Z14G. The toxicokinetics of Z14G were assessed after intravenous (IV) or oral administration (PO) in SD rats at doses of 10 mg/kg·b.w. In addition, comparative work with the parent mycotoxin ZEN was performed in parallel. The determination of Z14G and its metabolites (ZEN, α-zearalenol, β-zearalenol, α-zearalanol, β-zearalanol) proceeded with a sensitive UHPLC-MS/MS method. Our research indicated that Z14G readily disappeared from the blood, and distributed throughout the tissues via transformation into its parent form ZEN, and excreted primarily through urine. More importantly, the metabolite α-ZEL was observed in most analyzed tissue, urine and feces samples. Overall, our findings highlight the importance of biotransformation with regard to Z14G, providing critical insight for the health risk assessment of co-exposure of humans to glucoside-type modified mycotoxins.
first_indexed 2024-04-12T17:26:56Z
format Article
id doaj.art-0334b4ca27b0469c81d7bb29e375fe3d
institution Directory Open Access Journal
issn 0147-6513
language English
last_indexed 2024-04-12T17:26:56Z
publishDate 2022-11-01
publisher Elsevier
record_format Article
series Ecotoxicology and Environmental Safety
spelling doaj.art-0334b4ca27b0469c81d7bb29e375fe3d2022-12-22T03:23:16ZengElsevierEcotoxicology and Environmental Safety0147-65132022-11-01246114184Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in ratsQian Lu0Ming Sui1Ya-Wen Luo2Jiao-Yang Luo3Mei-Hua Yang4Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, ChinaKey Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, ChinaKey Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, ChinaCorresponding authors.; Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, ChinaCorresponding authors.; Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, ChinaBioaccumulation and biotransformation are critical factors that affect the release of easily metabolizable chemicals to cause human toxicity. The glucoside-type modified mycotoxin Zearalenone-14-Glucoside (Z14G) has attracted global attention for its high occurrence in foodstuffs and the potential threat to humans as its high rate of transformation into parent forms. Given the limited toxicokinetics information, this study assessed the absorption, distribution, biotransformation and excretion of Z14G, aiming to define the potential risk of Z14G. The toxicokinetics of Z14G were assessed after intravenous (IV) or oral administration (PO) in SD rats at doses of 10 mg/kg·b.w. In addition, comparative work with the parent mycotoxin ZEN was performed in parallel. The determination of Z14G and its metabolites (ZEN, α-zearalenol, β-zearalenol, α-zearalanol, β-zearalanol) proceeded with a sensitive UHPLC-MS/MS method. Our research indicated that Z14G readily disappeared from the blood, and distributed throughout the tissues via transformation into its parent form ZEN, and excreted primarily through urine. More importantly, the metabolite α-ZEL was observed in most analyzed tissue, urine and feces samples. Overall, our findings highlight the importance of biotransformation with regard to Z14G, providing critical insight for the health risk assessment of co-exposure of humans to glucoside-type modified mycotoxins.http://www.sciencedirect.com/science/article/pii/S0147651322010247Zearalenone-14-GlucosideToxicokineticTissue distributionExcretionBiotransformationUHPLC-q-trap-MS/MS
spellingShingle Qian Lu
Ming Sui
Ya-Wen Luo
Jiao-Yang Luo
Mei-Hua Yang
Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
Ecotoxicology and Environmental Safety
Zearalenone-14-Glucoside
Toxicokinetic
Tissue distribution
Excretion
Biotransformation
UHPLC-q-trap-MS/MS
title Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
title_full Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
title_fullStr Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
title_full_unstemmed Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
title_short Further insight into the potential toxicity of zearalenone-14-glucoside based on toxicokinetics, tissue distribution, transformation, and excretion in rats
title_sort further insight into the potential toxicity of zearalenone 14 glucoside based on toxicokinetics tissue distribution transformation and excretion in rats
topic Zearalenone-14-Glucoside
Toxicokinetic
Tissue distribution
Excretion
Biotransformation
UHPLC-q-trap-MS/MS
url http://www.sciencedirect.com/science/article/pii/S0147651322010247
work_keys_str_mv AT qianlu furtherinsightintothepotentialtoxicityofzearalenone14glucosidebasedontoxicokineticstissuedistributiontransformationandexcretioninrats
AT mingsui furtherinsightintothepotentialtoxicityofzearalenone14glucosidebasedontoxicokineticstissuedistributiontransformationandexcretioninrats
AT yawenluo furtherinsightintothepotentialtoxicityofzearalenone14glucosidebasedontoxicokineticstissuedistributiontransformationandexcretioninrats
AT jiaoyangluo furtherinsightintothepotentialtoxicityofzearalenone14glucosidebasedontoxicokineticstissuedistributiontransformationandexcretioninrats
AT meihuayang furtherinsightintothepotentialtoxicityofzearalenone14glucosidebasedontoxicokineticstissuedistributiontransformationandexcretioninrats