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  • Detection of zearalenone and its metabolites in naturally contaminated porcine follicular fluid by using liquid chromatography-tandem mass spectrometry.

Detection of zearalenone and its metabolites in naturally contaminated porcine follicular fluid by using liquid chromatography-tandem mass spectrometry.

The Journal of reproduction and development (2010-12-09)
Rentsenkhand Sambuu, Mitsuhiro Takagi, Satoshi Shiga, Seiichi Uno, Emiko Kokushi, Zhao Namula, Takeshige Otoi, Akio Miyamoto, Eisaburo Deguchi, Johanna Fink-Gremmels
ABSTRACT

Zearalenone (ZEN) and its metabolites are important nonsteroidal estrogenic mycotoxins that cause reproductive disorders in domestic animals, especially pigs. We aimed to simultaneously detect ZEN and its metabolites á-zearalenol (α-ZOL) and β-zearalenol (β-ZOL) in porcine follicular fluid (FF) by liquid chromatography-tandem mass spectrometry. ZEN and α-ZOL, but not β-ZOL, were detected in all pooled FF samples collected from coexisting follicles (diameter ≥ 6 mm) within 10 ovaries. Furthermore, ZEN and α-ZOL were detected in samples pretreated with β-glucuronidase/arylsulfatase, but not in those left untreated, suggesting that the FF samples contained glucuronide-conjugated forms of the mycotoxins that may be less harmful to porcine oocytes due to glucuronidation affecting the receptor binding. Nonetheless, the effects of the glucuronide-conjugated forms should be studied, both in vitro and in vivo.

MATERIALS
Product Number
Brand
Product Description

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Sulfatase from Aerobacter aerogenes, Type VI, buffered aqueous glycerol solution, 2-5 units/mg protein (biuret), 10-20 units/mL
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Sulfatase from Helix pomatia, Type H-1, sulfatase ≥10,000 units/g solid
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Sulfatase from Patella vulgata (keyhole limpet), Type IV, essentially salt-free, lyophilized powder, ≥10 units/mg solid
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Sulfatase from Helix pomatia, Type H-2, aqueous solution, ≥2,000 units/mL
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Sulfatase from abalone entrails, Type VIII, lyophilized powder, 20-40 units/mg solid