Cargando…
In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure
Ochratoxin A (OTA) is a widespread food contaminant, with exposure estimated to range from 0.64 to 17.79 ng/kg body weight (bw) for average consumers and from 2.40 to 51.69 ng/kg bw per day for high consumers. Current exposure estimates are, however, associated with considerable uncertainty. While b...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402547/ https://www.ncbi.nlm.nih.gov/pubmed/34437458 http://dx.doi.org/10.3390/toxins13080587 |
_version_ | 1783745816008065024 |
---|---|
author | Dekant, Raphael Langer, Michael Lupp, Maria Adaku Chilaka, Cynthia Mally, Angela |
author_facet | Dekant, Raphael Langer, Michael Lupp, Maria Adaku Chilaka, Cynthia Mally, Angela |
author_sort | Dekant, Raphael |
collection | PubMed |
description | Ochratoxin A (OTA) is a widespread food contaminant, with exposure estimated to range from 0.64 to 17.79 ng/kg body weight (bw) for average consumers and from 2.40 to 51.69 ng/kg bw per day for high consumers. Current exposure estimates are, however, associated with considerable uncertainty. While biomarker-based approaches may contribute to improved exposure assessment, there is yet insufficient data on urinary metabolites of OTA and their relation to external dose to allow reliable estimates of daily intake. This study was designed to assess potential species differences in phase II biotransformation in vitro and to establish a correlation between urinary OTA-derived glucuronides and mercapturic acids and external exposure in rats in vivo. In vitro analyses of OTA metabolism using the liver S9 of rats, humans, rabbits and minipigs confirmed formation of an OTA glucuronide but provided no evidence for the formation of OTA-derived mercapturic acids to support their use as biomarkers. Similarly, OTA-derived mercapturic acids were not detected in urine of rats repeatedly dosed with OTA, while indirect analysis using enzymatic hydrolysis of the urine samples prior to LC–MS/MS established a linear relationship between urinary glucuronide excretion and OTA exposure. These results support OTA-derived glucuronides but not mercapturic acids as metabolites suitable for biomonitoring. |
format | Online Article Text |
id | pubmed-8402547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84025472021-08-29 In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure Dekant, Raphael Langer, Michael Lupp, Maria Adaku Chilaka, Cynthia Mally, Angela Toxins (Basel) Article Ochratoxin A (OTA) is a widespread food contaminant, with exposure estimated to range from 0.64 to 17.79 ng/kg body weight (bw) for average consumers and from 2.40 to 51.69 ng/kg bw per day for high consumers. Current exposure estimates are, however, associated with considerable uncertainty. While biomarker-based approaches may contribute to improved exposure assessment, there is yet insufficient data on urinary metabolites of OTA and their relation to external dose to allow reliable estimates of daily intake. This study was designed to assess potential species differences in phase II biotransformation in vitro and to establish a correlation between urinary OTA-derived glucuronides and mercapturic acids and external exposure in rats in vivo. In vitro analyses of OTA metabolism using the liver S9 of rats, humans, rabbits and minipigs confirmed formation of an OTA glucuronide but provided no evidence for the formation of OTA-derived mercapturic acids to support their use as biomarkers. Similarly, OTA-derived mercapturic acids were not detected in urine of rats repeatedly dosed with OTA, while indirect analysis using enzymatic hydrolysis of the urine samples prior to LC–MS/MS established a linear relationship between urinary glucuronide excretion and OTA exposure. These results support OTA-derived glucuronides but not mercapturic acids as metabolites suitable for biomonitoring. MDPI 2021-08-23 /pmc/articles/PMC8402547/ /pubmed/34437458 http://dx.doi.org/10.3390/toxins13080587 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dekant, Raphael Langer, Michael Lupp, Maria Adaku Chilaka, Cynthia Mally, Angela In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title | In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title_full | In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title_fullStr | In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title_full_unstemmed | In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title_short | In Vitro and In Vivo Analysis of Ochratoxin A-Derived Glucuronides and Mercapturic Acids as Biomarkers of Exposure |
title_sort | in vitro and in vivo analysis of ochratoxin a-derived glucuronides and mercapturic acids as biomarkers of exposure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402547/ https://www.ncbi.nlm.nih.gov/pubmed/34437458 http://dx.doi.org/10.3390/toxins13080587 |
work_keys_str_mv | AT dekantraphael invitroandinvivoanalysisofochratoxinaderivedglucuronidesandmercapturicacidsasbiomarkersofexposure AT langermichael invitroandinvivoanalysisofochratoxinaderivedglucuronidesandmercapturicacidsasbiomarkersofexposure AT luppmaria invitroandinvivoanalysisofochratoxinaderivedglucuronidesandmercapturicacidsasbiomarkersofexposure AT adakuchilakacynthia invitroandinvivoanalysisofochratoxinaderivedglucuronidesandmercapturicacidsasbiomarkersofexposure AT mallyangela invitroandinvivoanalysisofochratoxinaderivedglucuronidesandmercapturicacidsasbiomarkersofexposure |