2007
DOI: 10.1016/j.fct.2006.07.030
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Review on the toxicity, occurrence, metabolism, detoxification, regulations and intake of zearalenone: An oestrogenic mycotoxin

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Cited by 1,229 publications
(929 citation statements)
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References 141 publications
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“…A full MS scan performed for ZEN-4Glu did not show any detectable levels of this analyte which has been highlighted to be a possible biomarker for ZEN exposure [19]. In comparison to the findings of Massart et al [18], who reported occurrence of α-ZOL and ZEN in the serum of female subjects affected by precocious puberty in the United States, we detected three samples co-contamination of β-ZOL (3.3-20 ng mg -1 Crea) and ZEN (<LOQ-10.8 ng mg -1 Crea).…”
Section: Results Of Pilot Studymentioning
confidence: 92%
See 1 more Smart Citation
“…A full MS scan performed for ZEN-4Glu did not show any detectable levels of this analyte which has been highlighted to be a possible biomarker for ZEN exposure [19]. In comparison to the findings of Massart et al [18], who reported occurrence of α-ZOL and ZEN in the serum of female subjects affected by precocious puberty in the United States, we detected three samples co-contamination of β-ZOL (3.3-20 ng mg -1 Crea) and ZEN (<LOQ-10.8 ng mg -1 Crea).…”
Section: Results Of Pilot Studymentioning
confidence: 92%
“…Review on the toxicity, occurrence, metabolism and detoxification of ZEN suggested two major biotransformation pathways in animals: (1) hydroxylation resulting in the formation of alpha zearalenol (α-ZOL) and beta zearalenol (β-ZOL) assumed to be catalyzed by 3α and 3β hydroxyl steroid dehydrogenase respectively and (2) conjugation of ZEN and its reduced metabolites with glucuronic acid [19]. Till date, no paper has reported the presence of α-ZOL-glucuronide and β-ZOL-glucuronide in human urine samples.…”
Section: Introductionmentioning
confidence: 99%
“…Phase III comprises the compartmentalisation of the mycotoxins into the vacuole of the plant or binding to the cell wall (Berthiller et al, 2009a;Coleman et al, 1997;He et al, 2010;Zinedine et al, 2007). A potential risk for consumers is the possible hydrolysis of masked mycotoxins into their toxic parent forms during mammalian digestion (Grabley et al, 1992;Berthiller et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…As a result of the potential hazards associated with these toxins, many governments require regular monitoring for multiple mycotoxins and have set maximum residue limits for these compounds. The most prominent and most dangerous that are associated with food safety are the aflatoxins, ochratoxin A (OTA), ZEN, the T-2 toxins, and the penultimate precursor to AFB1, sterigmatocystin (ST) [3][4][5][6][7][8].…”
Section: Introductionmentioning
confidence: 99%