2019
DOI: 10.1080/10408398.2019.1655388
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Occurrence and toxicity of a fusarium mycotoxin, zearalenone

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Cited by 241 publications
(157 citation statements)
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“…In animals, including mice, pigs and cattle, ZEA can damage the reproductive organs and cause reproductive disorders [113,114]. Toxicokinetic studies prove that ZEA is absorbed in the digestive tract, and then metabolized and distributed to various parts of the body [120]. Zearalenone is a competitive substrate for enzymes involved in the synthesis and metabolism of steroids, and therefore can potentially act as a factor disturbing hormonal balance [121].…”
Section: Zearalenonementioning
confidence: 99%
“…In animals, including mice, pigs and cattle, ZEA can damage the reproductive organs and cause reproductive disorders [113,114]. Toxicokinetic studies prove that ZEA is absorbed in the digestive tract, and then metabolized and distributed to various parts of the body [120]. Zearalenone is a competitive substrate for enzymes involved in the synthesis and metabolism of steroids, and therefore can potentially act as a factor disturbing hormonal balance [121].…”
Section: Zearalenonementioning
confidence: 99%
“…most important agro-economic and public health classes of mycotoxins are aflatoxins, ochratoxin A (OTA), zearalenone (ZEA), trichothecenes (TCTs), fumonisins (FUMs), patulin (PT), Alternaria toxins and ergot toxins. They are produced by species of Fusarium, Penicillium, Aspergillus, Claviceps and Alternaria (Liew and Mohd-Redzwan, 2018;Rai et al, 2019). Some of them can produce more than one mycotoxin, and some mycotoxins are produced by more than one fungal species (Marin et al, 2013) ( Table 1).…”
Section: Most Susceptible Cropsmentioning
confidence: 99%
“…Zearalenone (ZEA) is one of the most prevalent nonsteroidal oestrogenic mycotoxins produced by Fusarium genera such as Fusarium graminearum, Fusarium culmorum, Fusarium crookwellense, Fusarium semitectum and Fusarium equiseti, which are distributed worldwide (Rai et al, 2019). ZEA and its major alcohol metabolites, α-zearalenol (α-ZOL), β-zearalenol (β-ZOL), α-zearalanol (α-ZAL, zeranol) and β-zearalanol (β-ZAL, tarelanol) share structural similarity with the sex hormone, 17β-estradiol, and can be found naturally or as result of metabolism of humans and animals (Danicke, 2015).…”
Section: Zearalenonementioning
confidence: 99%
“…It appears as a contaminant in crops, cereal-based products (e.g., flour, bakery goods, and beer), and in other commodities (Rogowska et al 2019). Despite its nonsteroidal structure, ZEN can bind to estrogen receptors (Loi et al 2017;Shier et al 2001) causing reproductive disorders, as well as its potential genotoxic, hepatotoxic, teratogenic, and immunotoxic effects are also suggested (Rai et al 2019;Rogowska et al 2019). The involvement of ZEN in the development of breast and esophageal cancers has been emerged; however, ZEN is classified as a group 3 carcinogen by the IARC (Rai et al 2019).…”
Section: Introductionmentioning
confidence: 99%
“…ZEN is extensively biotransformed in mammals (Rai et al 2019). Its reduction by hydroxysteroid dehydrogenases leads to the formation of αand β-zearalenols (α-and β-ZELs), zearalanone (ZAN, Fig.…”
Section: Introductionmentioning
confidence: 99%