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Zearalenone

February 15, 2024

Zearalenone (ZEN), also known as RAL and F-2 mycotoxin, is a potent estrogenic metabolite produced by some Fusarium and Gibberella species.[1] Specifically, the Gibberella zeae, the fungal species where zearalenone was initially detected, in its asexual/anamorph stage is known as Fusarium graminearum.[2] Several Fusarium species produce toxic substances of considerable concern to livestock and poultry producers, namely deoxynivalenol, T-2 toxin, HT-2 toxin, diacetoxyscirpenol (DAS) and zearalenone. Particularly, ZEN is produced by Fusarium graminearum, Fusarium culmorum, Fusarium cerealis, Fusarium equiseti,[3] Fusarium verticillioides,[4] and Fusarium incarnatum. Zearalenone is the primary toxin that binds to estrogen receptors, causing infertility, abortion or other breeding problems, especially in swine.[4] Often, ZEN is detected together with deoxynivalenol in contaminated samples and its toxicity needs to be considered in combination with the presence of other toxins.[5]

Zearalenone
Names
Preferred IUPAC name
(3S,11E)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione
Other names
Mycotoxin F2
Identifiers
  • 17924-92-4 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:10106 Y
ChEMBL
  • ChEMBL454173 Y
ChemSpider
  • 4444897 Y
ECHA InfoCard 100.038.043
KEGG
  • C09981 Y
  • 5281576
UNII
  • 5W827M159J Y
  • DTXSID0021460
  • InChI=1S/C18H22O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h3,7,10-12,20-21H,2,4-6,8-9H2,1H3/b7-3+/t12-/m0/s1 Y
    Key: MBMQEIFVQACCCH-QBODLPLBSA-N Y
  • InChI=1/C18H22O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h3,7,10-12,20-21H,2,4-6,8-9H2,1H3/b7-3+/t12-/m0/s1
    Key: MBMQEIFVQACCCH-QBODLPLBBS
  • C[C@H]1CCCC(=O)CCC/C=C/c2cc(cc(c2C(=O)O1)O)O
Properties
C18H22O5
Molar mass 318.369 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

Zearalenone is heat-stable and is found worldwide in a number of cereal crops, such as maize, barley, oats, wheat, rice, and sorghum.[6][7][8] Its production increases when the climate is warm with air humidity at or above twenty percent. [4] The environmental pH plays also a role in the toxin's production. When temperatures fall to 15oC, alkaline soils still support ZEN production. At the preferred Fusarium temperature, which ranges between 25oC and 30oC, neutral pH results in the greatest toxin production. [9]

In addition to its actions on the classical estrogen receptors, zearalenone has been found to act as an agonist of the GPER (GPR30).[8]

Chemical and physical properties edit

Zearalenone is a white crystalline solid, with molecular formula C18H22O5 and 318.364 g/mol molecular weight. It is a resorcyclic acid lactone. It exhibits blue-green fluorescence when excited by long wavelength ultraviolet (UV) light (360 nm) and a more intense green fluorescence when excited with short wavelength UV light (260 nm).[4] In methanol, UV absorption maxima occur at 236 (e = 29,700), 274 (e = 13,909) and 316 nm (e = 6,020). Maximum fluorescence in ethanol occurs with irradiation at 314 nm and with emission at 450 nm. Solubility in water is about 0.002 g/100 mL. It is slightly soluble in hexane and progressively more so in benzene, acetonitrile, methylene chloride, methanol, ethanol, and acetone. It is also soluble in aqueous alkali.[citation needed]

The naturally occurring isomer trans-zearalenone (trans-ZEN) is transformed by ultraviolet irradiation to cis-zearalenone (cis-ZEN).[10]

Metabolic pathways and products edit

Zearalenone is metabolically transformed to α-zearalenol (α-Zel) or (α-Zol), β-zearalenol (β-Zel) or (β-Zol), α-zearalanol (α-Zal), β-zearalanol (β-Zal), and zearalanone (ZAN) in animals. [9][11] The relative composition of these metabolic products varies by species. In pigs, cows and ducks, α-Zel is the dominant form detected.[12] [13][4] In humans, both α-Zel and β-Zel are seen in urine samples, with the beta form being prevalent.[14] In chickens, β-Zel is the dominant form and in plant cells, the metabolic product zeralenonne-14-O-β-glucoside has been detected.[4] Additionally, in the organs of animals these metabolic products are further modified to yield zearalenone-14-glucuronide (ZEN-14GlcA), α-zearalenol-glucuronide (α-Zel-14G) and β-zearalenol-glucuronide (β-Zel-14G).[15]

Dermal exposure edit

Zearalenone can permeate through the human skin.[16] However, no significant hormonal effects are expected after dermal contact in normal agricultural or residential environments.

Reproduction edit

Zearalenone structure is similar to estrogens and α-zearalenol binds with an even greater affinity estrogen receptors, while β-zearalenol's affinity is lower than both the parent compound's and α-Zel's binding affinity.[4] This identifies ZEN and its metabolites as xenoestrogens.[3] The human and livestock exposure to ZEN through the diet poses health concern due to the onset of several sexual disorders and alterations in the development of sexual apparatus.[17][18] There are reliable case reports of early puberty in girls chronically exposed to ZEN in various regions of the world.[19] In mice, ZEN consumption was linked to a decline of potent sperm and egg cells, an increase to double-stranded breaks in DNA and activation of DNA repair mechanisms, followed by embryonic development challenges that reduced the viability of offspring.[11]

Sampling and analysis edit

In common with other mycotoxins, sampling food commodities for zearalenone must be carried out to obtain samples representative of the consignment under test. Commonly used extraction solvents are aqueous mixtures of methanol, acetonitrile, or ethyl acetate followed by a range of different clean-up procedures that depend in part on the food and on the detection method in use. Thin-layer chromatography (TLC) methods and high-performance liquid chromatography (HPLC) are commonly used. The TLC method for zearalenone is: normal phase silica gel plates, the eluent: 90% dichloromethane, 10% v/v acetone; or reverse phase C18 silica plates; the eluent: 90% v/v methanol, 10% water. Zearalenone gives unmistakable blue luminiscence under UV.[1] HPLC alone is not sufficient, as it may often yield false positive results. Today, HPLC-MS/MS analysis is used to quantify and confirm the presence of zearalenone.

Typically, the representative sample is commuted and homogenized then few grams are used for extraction with acetonitrile/water mixture. The procedure is the widely used QuEChERS method that quickly and effectively extracts small molecules, like mycotoxins and pesticides, from complex food matrices and animal tissues. The determination step relies on liquid chromatography - mass-spectrometry (LC-MS/MS).[15] Another approach for the analysis of ZEA, without the requirement of expensive instrumentation, is developing specific peptide mimetic with the bioluminescent Gaussia luciferase fused as one protein that can bind specifically to ZEA.[20]

See also edit

References edit

  1. ^ a b "Zearalenone". Fermentek.
  2. ^ Liu J, Applegate T (June 2020). "Zearalenone (ZEN) in Livestock and Poultry: Dose, Toxicokinetics, Toxicity and Estrogenicity". Toxins. 12 (6): 377. doi:10.3390/toxins12060377. PMC 7354539. PMID 32517357.
  3. ^ a b Bulgaru CV, Marin DE, Pistol GC, Taranu I (March 2021). "Zearalenone and the Immune Response". Toxins. 13 (4): 248. doi:10.3390/toxins13040248. PMC 8066068. PMID 33807171.
  4. ^ a b c d e f g Ropejko K, Twarużek M (January 2021). "Zearalenone and Its Metabolites-General Overview, Occurrence, and Toxicity". Toxins. 13 (1): 35. doi:10.3390/toxins13010035. PMC 7825134. PMID 33418872.
  5. ^ Peillod C, Laborde M, Travel A, Mika A, Bailly JD, Cleva D, et al. (February 2021). "Toxic Effects of Fumonisins, Deoxynivalenol and Zearalenone Alone and in Combination in Ducks Fed the Maximum EUTolerated Level". Toxins. 13 (2): 152. doi:10.3390/toxins13020152. PMC 7920068. PMID 33669302.
  6. ^ Kuiper-Goodman T, Scott PM, Watanabe H (September 1987). "Risk assessment of the mycotoxin zearalenone". Regulatory Toxicology and Pharmacology. 7 (3): 253–306. doi:10.1016/0273-2300(87)90037-7. PMID 2961013.
  7. ^ Tanaka T, Hasegawa A, Yamamoto S, Lee US, Sugiura Y, Ueno Y (1988). "Worldwide Contamination of Cereals by the Fusarium Mycotoxins Nivalenol, Deoxynivalenol, and Zearalenone. 1. Survey of 19 Countries". Journal of Agricultural and Food Chemistry. American Chemical Society. 36 (5): 979–983. doi:10.1021/jf00083a019.
  8. ^ a b Prossnitz ER, Barton M (May 2014). "Estrogen biology: new insights into GPER function and clinical opportunities". Molecular and Cellular Endocrinology. 389 (1–2): 71–83. doi:10.1016/j.mce.2014.02.002. PMC 4040308. PMID 24530924.
  9. ^ a b Mahato DK, Devi S, Pandhi S, Sharma B, Maurya KK, Mishra S, et al. (January 2021). "Occurrence, Impact on Agriculture, Human Health, and Management Strategies of Zearalenone in Food and Feed: A Review". Toxins. 13 (2): 92. doi:10.3390/toxins13020092. PMC 7912641. PMID 33530606.
  10. ^ Brezina U, Kersten S, Valenta H, Sperfeld P, Riedel J, Dänicke S (November 2013). "UV-induced cis-trans isomerization of zearalenone in contaminated maize". Mycotoxin Research. 29 (4): 221–227. doi:10.1007/s12550-013-0178-7. PMID 24018604. S2CID 17466231.
  11. ^ a b Yang D, Jiang X, Sun J, Li X, Li X, Jiao R, et al. (September 2018). "Toxic effects of zearalenone on gametogenesis and embryonic development: A molecular point of review". Food and Chemical Toxicology. 119: 24–30. doi:10.1016/j.fct.2018.06.003. PMID 29864477. S2CID 46927149.
  12. ^ Peillod C, Laborde M, Travel A, Mika A, Bailly JD, Cleva D, et al. (February 2021). "Toxic Effects of Fumonisins, Deoxynivalenol and Zearalenone Alone and in Combination in Ducks Fed the Maximum EUTolerated Level". Toxins. 13 (2): 152. doi:10.3390/toxins13020152. PMC 7920068. PMID 33669302.
  13. ^ Gruber-Dorninger C, Faas J, Doupovec B, Aleschko M, Stoiber C, Höbartner-Gußl A, et al. (January 2021). "Metabolism of Zearalenone in the Rumen of Dairy Cows with and without Application of a Zearalenone-Degrading Enzyme". Toxins. 13 (2): 84. doi:10.3390/toxins13020084. PMC 7911295. PMID 33499402.
  14. ^ Al-Jaal B, Latiff A, Salama S, Hussain HM, Al-Thani NA, Al-Naimi N, et al. (April 2021). "Analysis of Multiple Mycotoxins in the Qatari Population and Their Relation to Markers of Oxidative Stress". Toxins. 13 (4): 267. doi:10.3390/toxins13040267. PMC 8068385. PMID 33917988.
  15. ^ a b Yan Z, Wang L, Wang J, Tan Y, Yu D, Chang X, et al. (March 2018). "A QuEChERS-Based Liquid Chromatography-Tandem Mass Spectrometry Method for the Simultaneous Determination of Nine Zearalenone-Like Mycotoxins in Pigs". Toxins. 10 (3): 129. doi:10.3390/toxins10030129. PMC 5869417. PMID 29558416.
  16. ^ Boonen J, Malysheva SV, Taevernier L, Diana Di Mavungu J, De Saeger S, De Spiegeleer B (November 2012). "Human skin penetration of selected model mycotoxins". Toxicology. 301 (1–3): 21–32. doi:10.1016/j.tox.2012.06.012. PMID 22749975.
  17. ^ Massart F, Saggese G (April 2010). "Oestrogenic mycotoxin exposures and precocious pubertal development". International Journal of Andrology. 33 (2): 369–376. doi:10.1111/j.1365-2605.2009.01009.x. PMID 20002219.
  18. ^ Schoevers EJ, Santos RR, Colenbrander B, Fink-Gremmels J, Roelen BA (August 2012). "Transgenerational toxicity of Zearalenone in pigs". Reproductive Toxicology. 34 (1): 110–119. doi:10.1016/j.reprotox.2012.03.004. PMID 22484360.
  19. ^ Hueza IM, Raspantini PC, Raspantini LE, Latorre AO, Górniak SL (March 2014). "Zearalenone, an estrogenic mycotoxin, is an immunotoxic compound". Toxins. 6 (3): 1080–1095. doi:10.3390/toxins6031080. PMC 3968378. PMID 24632555.
  20. ^ Peltomaa R, Fikacek S, Benito-Peña E, Barderas R, Head T, Deo S, et al. (September 2020). "Bioluminescent detection of zearalenone using recombinant peptidomimetic Gaussia luciferase fusion protein". Mikrochimica Acta. 187 (10): 547. doi:10.1007/s00604-020-04538-7. PMC 7938698. PMID 32886242.

External links edit

  •   Media related to Zearalenone at Wikimedia Commons
  • Eriksen GS, Pennington J, Schlatter J (2000). "Zearalenone". WHO International Programme on Chemical Safety - Safety Evaluation of Certain Food Additives and Contaminants. Inchem. WHO Food Additives Series.

February 15, 2024
zearalenone, also, known, mycotoxin, potent, estrogenic, metabolite, produced, some, fusarium, gibberella, species, specifically, gibberella, zeae, fungal, species, where, zearalenone, initially, detected, asexual, anamorph, stage, known, fusarium, graminearum. Zearalenone ZEN also known as RAL and F 2 mycotoxin is a potent estrogenic metabolite produced by some Fusarium and Gibberella species 1 Specifically the Gibberella zeae the fungal species where zearalenone was initially detected in its asexual anamorph stage is known as Fusarium graminearum 2 Several Fusarium species produce toxic substances of considerable concern to livestock and poultry producers namely deoxynivalenol T 2 toxin HT 2 toxin diacetoxyscirpenol DAS and zearalenone Particularly ZEN is produced by Fusarium graminearum Fusarium culmorum Fusarium cerealis Fusarium equiseti 3 Fusarium verticillioides 4 and Fusarium incarnatum Zearalenone is the primary toxin that binds to estrogen receptors causing infertility abortion or other breeding problems especially in swine 4 Often ZEN is detected together with deoxynivalenol in contaminated samples and its toxicity needs to be considered in combination with the presence of other toxins 5 Zearalenone NamesPreferred IUPAC name 3S 11E 14 16 Dihydroxy 3 methyl 3 4 5 6 9 10 hexahydro 1H 2 benzoxacyclotetradecine 1 7 8H dioneOther names Mycotoxin F2IdentifiersCAS Number 17924 92 4 Y3D model JSmol Interactive imageChEBI CHEBI 10106 YChEMBL ChEMBL454173 YChemSpider 4444897 YECHA InfoCard 100 038 043KEGG C09981 YPubChem CID 5281576UNII 5W827M159J YCompTox Dashboard EPA DTXSID0021460InChI InChI 1S C18H22O5 c1 12 6 5 9 14 19 8 4 2 3 7 13 10 15 20 11 16 21 17 13 18 22 23 12 h3 7 10 12 20 21H 2 4 6 8 9H2 1H3 b7 3 t12 m0 s1 YKey MBMQEIFVQACCCH QBODLPLBSA N YInChI 1 C18H22O5 c1 12 6 5 9 14 19 8 4 2 3 7 13 10 15 20 11 16 21 17 13 18 22 23 12 h3 7 10 12 20 21H 2 4 6 8 9H2 1H3 b7 3 t12 m0 s1Key MBMQEIFVQACCCH QBODLPLBBSSMILES C C H 1CCCC O CCC C C c2cc cc c2C O O1 O OPropertiesChemical formula C 18H 22O 5Molar mass 318 369 g mol 1Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox references Zearalenone is heat stable and is found worldwide in a number of cereal crops such as maize barley oats wheat rice and sorghum 6 7 8 Its production increases when the climate is warm with air humidity at or above twenty percent 4 The environmental pH plays also a role in the toxin s production When temperatures fall to 15oC alkaline soils still support ZEN production At the preferred Fusarium temperature which ranges between 25oC and 30oC neutral pH results in the greatest toxin production 9 In addition to its actions on the classical estrogen receptors zearalenone has been found to act as an agonist of the GPER GPR30 8 Contents 1 Chemical and physical properties 2 Metabolic pathways and products 3 Dermal exposure 4 Reproduction 5 Sampling and analysis 6 See also 7 References 8 External linksChemical and physical properties editZearalenone is a white crystalline solid with molecular formula C18H22O5 and 318 364 g mol molecular weight It is a resorcyclic acid lactone It exhibits blue green fluorescence when excited by long wavelength ultraviolet UV light 360 nm and a more intense green fluorescence when excited with short wavelength UV light 260 nm 4 In methanol UV absorption maxima occur at 236 e 29 700 274 e 13 909 and 316 nm e 6 020 Maximum fluorescence in ethanol occurs with irradiation at 314 nm and with emission at 450 nm Solubility in water is about 0 002 g 100 mL It is slightly soluble in hexane and progressively more so in benzene acetonitrile methylene chloride methanol ethanol and acetone It is also soluble in aqueous alkali citation needed The naturally occurring isomer trans zearalenone trans ZEN is transformed by ultraviolet irradiation to cis zearalenone cis ZEN 10 Metabolic pathways and products editZearalenone is metabolically transformed to a zearalenol a Zel or a Zol b zearalenol b Zel or b Zol a zearalanol a Zal b zearalanol b Zal and zearalanone ZAN in animals 9 11 The relative composition of these metabolic products varies by species In pigs cows and ducks a Zel is the dominant form detected 12 13 4 In humans both a Zel and b Zel are seen in urine samples with the beta form being prevalent 14 In chickens b Zel is the dominant form and in plant cells the metabolic product zeralenonne 14 O b glucoside has been detected 4 Additionally in the organs of animals these metabolic products are further modified to yield zearalenone 14 glucuronide ZEN 14GlcA a zearalenol glucuronide a Zel 14G and b zearalenol glucuronide b Zel 14G 15 Dermal exposure editZearalenone can permeate through the human skin 16 However no significant hormonal effects are expected after dermal contact in normal agricultural or residential environments Reproduction editZearalenone structure is similar to estrogens and a zearalenol binds with an even greater affinity estrogen receptors while b zearalenol s affinity is lower than both the parent compound s and a Zel s binding affinity 4 This identifies ZEN and its metabolites as xenoestrogens 3 The human and livestock exposure to ZEN through the diet poses health concern due to the onset of several sexual disorders and alterations in the development of sexual apparatus 17 18 There are reliable case reports of early puberty in girls chronically exposed to ZEN in various regions of the world 19 In mice ZEN consumption was linked to a decline of potent sperm and egg cells an increase to double stranded breaks in DNA and activation of DNA repair mechanisms followed by embryonic development challenges that reduced the viability of offspring 11 Sampling and analysis editIn common with other mycotoxins sampling food commodities for zearalenone must be carried out to obtain samples representative of the consignment under test Commonly used extraction solvents are aqueous mixtures of methanol acetonitrile or ethyl acetate followed by a range of different clean up procedures that depend in part on the food and on the detection method in use Thin layer chromatography TLC methods and high performance liquid chromatography HPLC are commonly used The TLC method for zearalenone is normal phase silica gel plates the eluent 90 dichloromethane 10 v v acetone or reverse phase C18 silica plates the eluent 90 v v methanol 10 water Zearalenone gives unmistakable blue luminiscence under UV 1 HPLC alone is not sufficient as it may often yield false positive results Today HPLC MS MS analysis is used to quantify and confirm the presence of zearalenone Typically the representative sample is commuted and homogenized then few grams are used for extraction with acetonitrile water mixture The procedure is the widely used QuEChERS method that quickly and effectively extracts small molecules like mycotoxins and pesticides from complex food matrices and animal tissues The determination step relies on liquid chromatography mass spectrometry LC MS MS 15 Another approach for the analysis of ZEA without the requirement of expensive instrumentation is developing specific peptide mimetic with the bioluminescent Gaussia luciferase fused as one protein that can bind specifically to ZEA 20 See also edita Zearalenol b Zearalenol Taleranol Trichothecene Zeranol ZearalanoneReferences edit a b Zearalenone Fermentek Liu J Applegate T June 2020 Zearalenone ZEN in Livestock and Poultry Dose Toxicokinetics Toxicity and Estrogenicity Toxins 12 6 377 doi 10 3390 toxins12060377 PMC 7354539 PMID 32517357 a b Bulgaru CV Marin DE Pistol GC Taranu I March 2021 Zearalenone and the Immune Response Toxins 13 4 248 doi 10 3390 toxins13040248 PMC 8066068 PMID 33807171 a b c d e f g Ropejko K Twaruzek M January 2021 Zearalenone and Its Metabolites General Overview Occurrence and Toxicity Toxins 13 1 35 doi 10 3390 toxins13010035 PMC 7825134 PMID 33418872 Peillod C Laborde M Travel A Mika A Bailly JD Cleva D et al February 2021 Toxic Effects of Fumonisins Deoxynivalenol and Zearalenone Alone and in Combination in Ducks Fed the Maximum EUTolerated Level Toxins 13 2 152 doi 10 3390 toxins13020152 PMC 7920068 PMID 33669302 Kuiper Goodman T Scott PM Watanabe H September 1987 Risk assessment of the mycotoxin zearalenone Regulatory Toxicology and Pharmacology 7 3 253 306 doi 10 1016 0273 2300 87 90037 7 PMID 2961013 Tanaka T Hasegawa A Yamamoto S Lee US Sugiura Y Ueno Y 1988 Worldwide Contamination of Cereals by the Fusarium Mycotoxins Nivalenol Deoxynivalenol and Zearalenone 1 Survey of 19 Countries Journal of Agricultural and Food Chemistry American Chemical Society 36 5 979 983 doi 10 1021 jf00083a019 a b Prossnitz ER Barton M May 2014 Estrogen biology new insights into GPER function and clinical opportunities Molecular and Cellular Endocrinology 389 1 2 71 83 doi 10 1016 j mce 2014 02 002 PMC 4040308 PMID 24530924 a b Mahato DK Devi S Pandhi S Sharma B Maurya KK Mishra S et al January 2021 Occurrence Impact on Agriculture Human Health and Management Strategies of Zearalenone in Food and Feed A Review Toxins 13 2 92 doi 10 3390 toxins13020092 PMC 7912641 PMID 33530606 Brezina U Kersten S Valenta H Sperfeld P Riedel J Danicke S November 2013 UV induced cis trans isomerization of zearalenone in contaminated maize Mycotoxin Research 29 4 221 227 doi 10 1007 s12550 013 0178 7 PMID 24018604 S2CID 17466231 a b Yang D Jiang X Sun J Li X Li X Jiao R et al September 2018 Toxic effects of zearalenone on gametogenesis and embryonic development A molecular point of review Food and Chemical Toxicology 119 24 30 doi 10 1016 j fct 2018 06 003 PMID 29864477 S2CID 46927149 Peillod C Laborde M Travel A Mika A Bailly JD Cleva D et al February 2021 Toxic Effects of Fumonisins Deoxynivalenol and Zearalenone Alone and in Combination in Ducks Fed the Maximum EUTolerated Level Toxins 13 2 152 doi 10 3390 toxins13020152 PMC 7920068 PMID 33669302 Gruber Dorninger C Faas J Doupovec B Aleschko M Stoiber C Hobartner Gussl A et al January 2021 Metabolism of Zearalenone in the Rumen of Dairy Cows with and without Application of a Zearalenone Degrading Enzyme Toxins 13 2 84 doi 10 3390 toxins13020084 PMC 7911295 PMID 33499402 Al Jaal B Latiff A Salama S Hussain HM Al Thani NA Al Naimi N et al April 2021 Analysis of Multiple Mycotoxins in the Qatari Population and Their Relation to Markers of Oxidative Stress Toxins 13 4 267 doi 10 3390 toxins13040267 PMC 8068385 PMID 33917988 a b Yan Z Wang L Wang J Tan Y Yu D Chang X et al March 2018 A QuEChERS Based Liquid Chromatography Tandem Mass Spectrometry Method for the Simultaneous Determination of Nine Zearalenone Like Mycotoxins in Pigs Toxins 10 3 129 doi 10 3390 toxins10030129 PMC 5869417 PMID 29558416 Boonen J Malysheva SV Taevernier L Diana Di Mavungu J De Saeger S De Spiegeleer B November 2012 Human skin penetration of selected model mycotoxins Toxicology 301 1 3 21 32 doi 10 1016 j tox 2012 06 012 PMID 22749975 Massart F Saggese G April 2010 Oestrogenic mycotoxin exposures and precocious pubertal development International Journal of Andrology 33 2 369 376 doi 10 1111 j 1365 2605 2009 01009 x PMID 20002219 Schoevers EJ Santos RR Colenbrander B Fink Gremmels J Roelen BA August 2012 Transgenerational toxicity of Zearalenone in pigs Reproductive Toxicology 34 1 110 119 doi 10 1016 j reprotox 2012 03 004 PMID 22484360 Hueza IM Raspantini PC Raspantini LE Latorre AO Gorniak SL March 2014 Zearalenone an estrogenic mycotoxin is an immunotoxic compound Toxins 6 3 1080 1095 doi 10 3390 toxins6031080 PMC 3968378 PMID 24632555 Peltomaa R Fikacek S Benito Pena E Barderas R Head T Deo S et al September 2020 Bioluminescent detection of zearalenone using recombinant peptidomimetic Gaussia luciferase fusion protein Mikrochimica Acta 187 10 547 doi 10 1007 s00604 020 04538 7 PMC 7938698 PMID 32886242 External links edit nbsp Media related to Zearalenone at Wikimedia Commons Eriksen GS Pennington J Schlatter J 2000 Zearalenone WHO International Programme on Chemical Safety Safety Evaluation of Certain Food Additives and Contaminants Inchem WHO Food Additives Series Retrieved from https en wikipedia org w index php title Zearalenone amp oldid 1205489792, wikipedia, wiki, book, 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