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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Exposure Biomarkers and Histopathological Analysis in Pig Liver after Exposure to Mycotoxins under Field Conditions: Special Report on Fumonisin B1

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Συγγραφέας
Papatsiros V.G., Stylianaki I., Tsekouras N., Papakonstantinou G., Gómez-Nicolau N.S., Letsios M., Papaioannou N.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1089/fpd.2020.2867
Λέξη-κλειδί
aflatoxin B1
aflatoxin M1
alpha zearalanone
alpha zearalenone
beta zearalanone
beta zearalenone
biological marker
deepoxideoxynivalenol
fumonisin B1
mycotoxin
ochratoxin
unclassified drug
vomitoxin
zearalanone
zearalenone
biological marker
fumonisin
fumonisin B1
mycosis
mycotoxin
animal experiment
animal model
animal tissue
Article
cell vacuole
controlled study
disease severity
histopathology
Kupffer cell
limit of detection
limit of quantitation
liquid chromatography-mass spectrometry
liver
liver cell
liver histology
liver necrosis
megalocytosis
nonhuman
pig
priority journal
slaughterhouse
adverse event
animal
environmental exposure
isolation and purification
liquid chromatography
mass spectrometry
microbiology
pig
swine disease
veterinary medicine
Abattoirs
Animals
Biomarkers
Chromatography, Liquid
Environmental Exposure
Fumonisins
Liver
Mass Spectrometry
Mycoses
Mycotoxins
Swine
Swine Diseases
Mary Ann Liebert Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
Liver samples from finisher pigs were collected at the slaughterhouses for the analysis of zearalenone (ZEA), alfa-/beta-zearalenone (α-ZE, β-ZE), zearalanone (ZA), alfa-/beta-ZA (α-ZA, β-ZA), aflatoxin B1 (AFB1) and aflatoxin M1, fumonisin B1 (FB1), ochratoxin A (OTA) and ochratoxin B, deoxynivalenol and deepoxi-deoxynivalenol (DOM-1). For the analysis liquid chromatography-triple quadrupole coupled with mass spectrometry was applied. Liver samples with detected FB1 were further histopathologically evaluated after hematoxylin and eosin staining. Various levels of liver mycotoxins were detected in all farms. Pig livers with 2.91-8.30 μg/kg of FB1 were detected in three farms, estimate of 850-2400 μg/kg of FB1 intake, whereas 0.54 μg/kg of OTA was detected in one farm, estimate of 75 μg/kg of OTA intake. Moreover, pig livers with 0.30 μg/kg of ZEA, 1.87 μg/kg of α-ZE, and 0.63 μg/kg of β-ZE were detected in one farm, estimate with of 300 μg/kg of ZEA intake. The histopathological analysis revealed that the lesions' grading and necrosis grading were analogously increased when FB1 concentration increased from 2.91 to 4.36-8.30 μg/kg. The severity of megalocytosis was analogously increased with FB1 detection levels and particularly in levels of 4.36-8.3 μg/kg. However, the increased FB1 detection levels did not show analogous behavior with the severity of hepatic cell vacuolization. Results showed that FB1 remained the most critical risk factor in the Greek pig industry, whereas ZEA and AFB1 were also prevalent. The OTA contamination in pig farms raised a high risk for animal and human health. © 2021 Mary Ann Liebert, Inc., publishers.
URI
http://hdl.handle.net/11615/77881
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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