Porcine Hepatic Response to Fumonisin B1 in a Short Exposure Period: Fatty Acid Profile and Clinical Investigations
Autor: | R. Glávits, Omeralfaroug Ali, Hedvig Fébel, Judit Szabó-Fodor, Krisztián Balogh, Melinda Kovács, Arianna Zantomasi, András Szabó, Miklós Mézes |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
medicine.medical_specialty
040301 veterinary sciences oxidation Health Toxicology and Mutagenesis Aspartate transaminase lcsh:Medicine Toxicology liver 0403 veterinary science lipids 03 medical and health sciences chemistry.chemical_compound Blood serum Internal medicine medicine phospholipids 030304 developmental biology chemistry.chemical_classification 0303 health sciences biology Triglyceride lcsh:R Fatty acid 04 agricultural and veterinary sciences clinical chemistry Endocrinology blood serum chemistry Alanine transaminase Docosahexaenoic acid biology.protein histopathology piglet Arachidonic acid fumonisin b1 Polyunsaturated fatty acid |
Zdroj: | Toxins, Vol 11, Iss 11, p 655 (2019) Toxins Volume 11 Issue 11 |
ISSN: | 2072-6651 |
Popis: | Scarce studies have investigated the impact of fumonisin B1 (FB1) on the hepatic tissue fatty acid (FA) profile, and no study is available on piglets. A 10-day in vivo experiment was performed on seven piglets/group: control and FB1-fed animals (diet was contaminated with fungal culture: 20 mg FB1/kg diet). Independent sample t-test was carried out at p < 0.05 as the significance level. Neither growth, nor feed efficiency, was affected. The hepatic phospholipid (PL) fatty acids (FAs) were more susceptible for FB1, while triglyceride (TG) was less responsive. The impact of FB1 on hepatic PL polyunsaturated fatty acids (PUFAs) was more pronounced than on saturated fatty acids. Among all PUFAs, predominant ones in response were docosapentaenoicacid (DPA) (&darr ), docosahexaenoic DHA (&darr ) and arachidonic acids (&uarr ). This led to a higher omega-6:omega-3 ratio, whereas a similar finding was noted in TGs. Neither total saturation (SFA) nor total monousaturation (MUFA) were affected by the FB1 administration. The liver showed an increase in malondialdehyde, as well as antioxidant capacity (reduced glutathione and glutathione peroxidase). The plasma enzymatic assessment revealed an increase in alkaline phosphatase (ALP), while alanine transaminase (ALT), aspartate transaminase (AST), lactate dehydrogenase (LDH), and gamma-glutamyltransferase (GGT) were not influenced. The microscopic sections provided evidence of vacuolar degeneration of the hepatocytes&rsquo cytoplasm, but it was not severe. Furthermore, the lung edema was developed, while the kidney was not affected. In conclusion, regarding FB1-mediated hepatotoxicity in piglets, the potential effect of slight hepatotoxicity did not compromise growth performance, at least at the dose and exposure period applied. |
Databáze: | OpenAIRE |
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