Literature DB >> 23605616

Proposal for a uniform designation of zearalenone and its metabolites.

Manfred Metzler1.   

Abstract

The Fusarium mycotoxin zearalenone is a frequent contaminant of food and feed. Up to now, different abbreviations and counting systems for the numerous positions of this macrocyclic ß-resorcylic acid lactone and its metabolites have been used. As the number of identified fungal and mammalian metabolites of zearalenone is still growing, the lack of a uniform designation makes the literature on these important toxins confusing and complicated. Here, we propose a logical set of abbreviations and a simple counting system, in order to facilitate future research communications on zearalenone and its congeners.

Entities:  

Year:  2010        PMID: 23605616     DOI: 10.1007/s12550-010-0075-2

Source DB:  PubMed          Journal:  Mycotoxin Res        ISSN: 0178-7888            Impact factor:   3.833


  8 in total

1.  Isolation of an anabolic, uterotrophic compound from corn infected with Gibberella zeae.

Authors:  M STOB; R S BALDWIN; J TUITE; F N ANDREWS; K G GILLETTE
Journal:  Nature       Date:  1962-12-29       Impact factor: 49.962

2.  Identification of an aliphatic epoxide and the corresponding dihydrodiol as novel congeners of zearalenone in cultures of Fusarium graminearum.

Authors:  Erika Pfeiffer; Andreas A Hildebrand; Christina Becker; Christian Schnattinger; Sandra Baumann; Andreas Rapp; Helmut Goesmann; Christoph Syldatk; Manfred Metzler
Journal:  J Agric Food Chem       Date:  2010-10-26       Impact factor: 5.279

Review 3.  Review on the toxicity, occurrence, metabolism, detoxification, regulations and intake of zearalenone: an oestrogenic mycotoxin.

Authors:  Abdellah Zinedine; Jose Miguel Soriano; Juan Carlos Moltó; Jordi Mañes
Journal:  Food Chem Toxicol       Date:  2006-08-30       Impact factor: 6.023

Review 4.  Risk assessment of the mycotoxin zearalenone.

Authors:  T Kuiper-Goodman; P M Scott; H Watanabe
Journal:  Regul Toxicol Pharmacol       Date:  1987-09       Impact factor: 3.271

5.  Aromatic hydroxylation and catechol formation: a novel metabolic pathway of the growth promotor zeranol.

Authors:  Andreas Hildebrand; Erika Pfeiffer; Manfred Metzler
Journal:  Toxicol Lett       Date:  2009-11-18       Impact factor: 4.372

6.  Zearanol metabolism by subcellular fractions from lamb liver.

Authors:  G Pompa; C Montesissa; F M Di Lauro; L Fadini; C Capua
Journal:  J Vet Pharmacol Ther       Date:  1988-06       Impact factor: 1.786

7.  Aromatic hydroxylation is a major metabolic pathway of the mycotoxin zearalenone in vitro.

Authors:  Erika Pfeiffer; Andreas Hildebrand; Georg Damm; Andreas Rapp; Benedikt Cramer; Hans-Ulrich Humpf; Manfred Metzler
Journal:  Mol Nutr Food Res       Date:  2009-09       Impact factor: 5.914

8.  The metabolism of zearalenone in subcellular fractions from rabbit and hen hepatocytes and its estrogenic activity in rabbits.

Authors:  G Pompa; C Montesissa; F M Di Lauro; L Fadini
Journal:  Toxicology       Date:  1986-12-01       Impact factor: 4.221

  8 in total
  11 in total

1.  Estrogenic in vitro evaluation of zearalenone and its phase I and II metabolites in combination with soy isoflavones.

Authors:  Dino Grgic; Andrea Betschler; Rebeka Früholz; Barbara Novak; Elisabeth Varga; Doris Marko
Journal:  Arch Toxicol       Date:  2022-08-20       Impact factor: 6.168

2.  A QuEChERS-Based Liquid Chromatography-Tandem Mass Spectrometry Method for the Simultaneous Determination of Nine Zearalenone-Like Mycotoxins in Pigs.

Authors:  Zheng Yan; Lan Wang; Jun Wang; Yanglan Tan; Dianzhen Yu; Xiaojiao Chang; Yingying Fan; Duoyong Zhao; Cheng Wang; Marthe De Boevre; Sarah De Saeger; Changpo Sun; Aibo Wu
Journal:  Toxins (Basel)       Date:  2018-03-20       Impact factor: 4.546

3.  Hydroxylation of the mycotoxin zearalenone at aliphatic positions: novel mammalian metabolites.

Authors:  Andreas A Hildebrand; Erika Pfeiffer; Andreas Rapp; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2011-09-08       Impact factor: 3.833

4.  Genotoxicity and inactivation of catechol metabolites of the mycotoxin zearalenone.

Authors:  Stefanie C Fleck; Andreas A Hildebrand; Elisabeth Müller; Erika Pfeiffer; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2012-09-27       Impact factor: 3.833

5.  Catechol metabolites of the mycotoxin zearalenone are poor substrates but potent inhibitors of catechol-O-methyltransferase.

Authors:  Erika Pfeiffer; Daniel Wefers; Andreas A Hildebrand; Stefanie C Fleck; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2013-04-05       Impact factor: 3.833

6.  1H NMR and MVA metabolomic profiles of urines from piglets fed with boluses contaminated with a mixture of five mycotoxins.

Authors:  Sandra A De Pascali; Lucia Gambacorta; Isabelle P Oswald; Laura Del Coco; Michele Solfrizzo; Francesco Paolo Fanizzi
Journal:  Biochem Biophys Rep       Date:  2017-05-25

7.  Synthesis of Mono- and Di-Glucosides of Zearalenone and α-/β-Zearalenol by Recombinant Barley Glucosyltransferase HvUGT14077.

Authors:  Herbert Michlmayr; Elisabeth Varga; Francesca Lupi; Alexandra Malachová; Christian Hametner; Franz Berthiller; Gerhard Adam
Journal:  Toxins (Basel)       Date:  2017-02-09       Impact factor: 4.546

Review 8.  Mycotoxins during the Processes of Nixtamalization and Tortilla Production.

Authors:  Sara Schaarschmidt; Carsten Fauhl-Hassek
Journal:  Toxins (Basel)       Date:  2019-04-16       Impact factor: 4.546

9.  Controlled Production of Zearalenone-Glucopyranoside Standards with Cunninghamella Strains Using Sulphate-Depleted Media.

Authors:  Jeroen Peters; Edward Ash; Arjen Gerssen; Ruud Van Dam; Maurice C R Franssen; Michel W F Nielen
Journal:  Toxins (Basel)       Date:  2021-05-21       Impact factor: 4.546

10.  Colour-encoded paramagnetic microbead-based direct inhibition triplex flow cytometric immunoassay for ochratoxin A, fumonisins and zearalenone in cereals and cereal-based feed.

Authors:  Jeroen Peters; Darren Thomas; Ed Boers; Theo de Rijk; Franz Berthiller; Willem Haasnoot; Michel W F Nielen
Journal:  Anal Bioanal Chem       Date:  2013-06-13       Impact factor: 4.142

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