Algal and Fungal Toxins 1971
DOI: 10.1016/b978-0-12-046507-1.50010-0
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F-2(Zearalenone) Estrogenic Mycotoxin from Fusarium

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Cited by 69 publications
(61 citation statements)
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“…Produced by P. oxalicum, it is part of the secalonic acid family and is teratogenic in mice (112). Zearalenone has been found in dust and aerosols and may cause infertility and fetal malformations in domestic animals through estrogenic effects discussed above (69,211,272). OA may cause fetal death, as well as uterohemorrhagic effects, in rats (211, 400).…”
Section: Pregnancymentioning
confidence: 99%
“…Produced by P. oxalicum, it is part of the secalonic acid family and is teratogenic in mice (112). Zearalenone has been found in dust and aerosols and may cause infertility and fetal malformations in domestic animals through estrogenic effects discussed above (69,211,272). OA may cause fetal death, as well as uterohemorrhagic effects, in rats (211, 400).…”
Section: Pregnancymentioning
confidence: 99%
“…Swine is the animal species most susceptible to the toxic effects of zearalenone and atrazine, in which these agents cause vulvovaginitis with persistent estrus, possible vaginal and rectal prolapse, and abortion in pregnant animals (Mirocha et al, 1971;Chang et al, 1979;Blaney et al, 1984). Atrazine, on the other hand, induces anestrus, as it was found to significantly increase the concentration of progesterone and decrease the concentration of 17β-estradiol in serum when given in feed in a dose of 2 mg/kg body weight (b.w.)…”
Section: Introductionmentioning
confidence: 99%
“…is quite common in this climate zone, ranging from 20% (Munk and Topolko, 1978;Mitak et al, 2001) to even 82% (Kralj et al, 1988), depending on weather conditions. Zearalenone induces characteristic changes, mainly in swine, which are known as the vulvovaginitis syndrome followed by a continuous estrus (Mirocha et al, 1971;Chang et al, 1979;Blaney et al, 1984;Glavits and Vanyi, 1995), and reproduction impairments caused by lower concentrations of zearalenone (Kordic et al, 1992;Vanyi et al, 1994). The physiological activity of zearalenone and its derivatives can be explained by their competition with 17β-estradiol for the specific receptor binding site and interference with steroid enzymes (Kiang et al, 1978;Boyd and Witliff, 1978;Kiessling and Petterson, 1978;Thouvenot and Morfin, 1980;Olsen et al, 1981Olsen et al, , 1985.…”
mentioning
confidence: 99%