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2012 | 68 | 09 |

Tytuł artykułu

Znaczenie diagnostyczne wybranych wyników laboratoryjnych mikotoksykozy zearalenonowej zwierząt

Warianty tytułu

EN
Diagnostic significance of selected analytical indicators of zearalenone mycotoxicosis in animals

Języki publikacji

PL

Abstrakty

EN
Mycotoxicosis has long been studied in humans and animals. Zearalenone-induced mycotoxicosis poses a growing problem in companion animals and livestock. The objective of this study was to determine whether intoxication with low doses of zearalenone (ZEA) and its biotransformation in selected animal species affects hematological and serum biochemical indices, as well as endocrine, intracrine and immunohistochemical parameters. Materials and Methods. Experiment I was performed on 36 gilts with a body weight of ± 20 kg. Half of the animals (18 gilts) were administered ZEA at a daily dose of 40 ìg/kg BW, and the remaining gilts were the placebo group. The experiment lasted 42 days. The animals were slaughtered at the end of the experiment (day 42), and samples were collected for laboratory analyses. Experiment II was performed on 30 clinically healthy pre-pubertal beagle bitches aged 70 days, with the initial body weight of ± 8 kg. The dogs were randomly divided into two experimental groups (EI and EII) and a control group (C). The experimental groups were administered per os ZEA doses of 50 and 75 ìg/kg BW, respectively, for 42 days. The control group bitches were administered placebo. The animals were subjected to ovariohysterectomy at the end of the experiment. Results and Discussion. The type of cell death induced by ZEA was very difficult to define in both groups of animals. Cell apoptosis and/or necrosis is determined by the cell’s energy resources, which reflect the level of mitochondrial metabolic activity. ZEA-induced damage of the cell membrane probably reduced the mitochondrial membrane potential. The above led to a decrease in ATP levels, which play an important role in the cell death process. In the presence of a toxic substance, such as ZEA, cell apoptosis and/or necrosis can be induced by the same factor as part of the hormetic response. The death of the cells studied here was induced by excessive Ca²⁺ levels in the mitochondria, mitochondrial dysfunction and a decrease or loss of mitochondrial metabolic activity in oocytes, follicular cells and interstitial cells in the ovaries of experimental bitches and gilts. Low doses of ZEA reduced the number of ERβ receptors, the only receptors in the ovaries, which activated epigenetic modification mechanisms and inhibited ovarian development. The increase in E2 concentrations was proportional to the degree of intoxication, which resulted from specific enzymatic regulation in the presence of ZEA as a competitive substrate that modulates the activity of enzymes participating in estrogen biosynthesis at the pre-receptor level and very low concentrations of á-zearalenol due to slow biotransformation of ZEA. Hyperestrogenism was observed, and the hormetic threshold dose level was clearly exceeded in the experimental groups. No changes were found in the hematological and serum biochemical parameters of the gilts and bitches.

Wydawca

-

Rocznik

Tom

68

Numer

09

Opis fizyczny

s.566-570,bibliogr.

Twórcy

autor
  • Katedra Prewencji Weterynaryjnej i Higieny Pasz, Wydział Medycyny Weterynaryjnej, Uniwersytet Warmińsko-Mazurski w Olsztynie, ul.Oczapowskiego 13/29, 10-718 Olsztyn
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Bibliografia

  • 1.Dworakowska D.: Apoptotic index and selected cell cycle regulators in non-small cell lung cancer. Ann. Acad. Med. Gedanensis 2005, 35, 1-112.
  • 2.Gajęcka M., Jakimiuk E., Zielonka Ł., Obremski K., Gajęcki M.: The biotransformation of chosen mycotoxins. Pol. J. Vet. Sci. 2009, 12, 293-303.
  • 3.Gajęcka M., Obremski K., Jakimiuk E., Skorska-Wyszyńska E., Zielonka Ł., Gajęcki M.: Histopathological examination of ovaries in bitches after experimental zearalenone micotoxicosis. Pol. J. Vet. Sci. 2008, 11, 363-366.
  • 4.Gajęcka M., Woźny M., Brzuzan P., Zielonka Ł., Gajęcki M.: Expression of CYPscc and 3β-HSD mRNA in bitches ovary after long-term exposure to zearalenone. Bull. Vet. Inst. Pulawy 2011, 55, 777-780.
  • 5.Gajęcki M., Gajęcka M., Jakimiuk E., Zielonka Ł., Obremski K.: Zearalenone - undesirable substance, [w:] Mahendra Rai, Ajit Varma (Eds.): Mycotoxins in Food, Feed and Bioweapons. Springer-Verlag Berlin Heidelberg 2010, 131-144.
  • 6.Gunter T. E., Sheu S.-S.: Characteristics and possible functions of mitochondrial Ca²⁺ transport mechanisms. BBA-Bioenergetics 2009, 1787, 1291-1308.
  • 7.Hatoya S., Torii R., Kumagai D., Sugiura K., Kawate N., Tamada H., Sawada T., Inaba T.: Expression of estrogen receptor a and b genes in the mediobasal hypothalamus, pituitary and ovary during the canine estrous cycle. Neurosci. Lett. 2003, 347, 131-135.
  • 8.Kuciel-Lisieska G., Obremski K., Stelmachów J., Gajęcka M., Zielonka Ł., Jakimiuk E., Gajęcki M.: The presence of zearalenone in blood plasma in women with neoplastic lesions in a mammary gland. Bull. Vet. Inst. Pulawy 2008, 52, 671-674.
  • 9.Łabędzka K., Grzanka A., Izdebska M.: Mitochondria and cell heath. Postepy Hig. Med. Dosw. (online) 2006, 60, 439-446.
  • 10.Matwee C., Betts D. H., King W. A.: Apoptosis in the early bovine embryo. Zygote 2000, 8, 57-68.
  • 11.Moreira P. I., Custódio J. B. A., Nunes E., Oliveira P. J., Moreno A., Seica R., Oliveira C. R., Santos M. S.: Mitochondria from distinct tissues are differently affected by 17β-estradiol and tamoxifen. J. Steroid Biochem. 2011, 123, 8-16.
  • 12.Penning T. M.: Human hydroxysteroid dehydrogenases and pre-receptor regulation: Insights into inhibitor design and evaluation. J. Steroid Biochem. 2011, 125, 46-56.
  • 13.Plewka A.: The metabolism of xenobiotics in alimentary system with special regard to the role of large intestine. Proc. VII International Scientific Conference: Veterinary Feed Hygiene - The Effects of Mycotoxins on Gastrointestinal Function. 23-24 September 2011, Olsztyn, Poland, s. 60-69.
  • 14.Scotti L., Irusta G., Abramovich D., Tesone M., Parborell F.: Administration of a gonadotropin-releasing hormone agonist affects corpus luteum vascular stability and development and induces luteal apoptosis in a rat model of ovarian hyperstimulation syndrome. Mol. Cell. Endocrinol. 2011, 335, 116-125.
  • 15.Singh M. N., Stringfellow H. F., Paraskevaidis E., Martin-Hirsch P. L., Martin F. L.: Tamoxifen: important considerations of a multifunctional compound with organ-specific properties. Cancer Treat. Rev. 2007, 33, 91-100.
  • 16.Słomczyńska M.: The dynamic of the steroid hormone receptors distribution in the ovary. Post. Biol. Kom. 2002, 29, 27-46.
  • 17.Takemura H., Joong-Youn S., Kazutoshi S., Airo T., Bao T. Z., Kayoko S.: Characterization of the estrogenic activities of zearalenone and zeranol in vivo and in vitro. J. Steroid Biochem. 2007, 103, 170-177.
  • 18.Wąsowicz K., Chmielewska M., Łosiewicz K.: Estrogen receptors - morphology, physiology, pathology. Proc. VII International Scientific Conference: Veterinary Feed Hygiene - The Effects of Mycotoxins on Gastrointestinal Function. 23-24 September 2011, Olsztyn, Poland, s. 56-59.
  • 19.Zinedine A., Soriano J. M., Moltó J. C., Mañes J.: Review on the toxicity, occurrence, metabolism, detoxification, regulations and intake of zearalenone: An oestrogenic mycotoxin. Food Chem. Toxicol. 2007, 45, 1-18.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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