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1.
Exp Toxicol Pathol ; 67(2): 89-98, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-25467749

RESUMO

Deoxynivalenol (DON), nivalenol (NIV) and zearalenone (ZEA) are mycotoxins commonly produced by Fusarium species. The purpose of the present study was to investigate the effects of DON alone and in combination with NIV and ZEA on several parameters including weight gain and histological aspects of pigs submitted to chronic intoxication. Twenty, 5-week-old piglets received for 28 days one of the following diets: a control diet, a diet mono- contaminated with DON (1.5mg/kg), a diet multi-contaminated with DON (2mg/kg)+NIV (1.3mg/kg)+ZEA (1.5mg/kg) or a diet contaminated with DON (3mg/kg)+NIV (1.3mg/kg)+ZEA (1.5mg/kg). Animals fed the multi-contaminated diets presented a significant decrease in weight gain over the total period. The chronic ingestion of the contaminated diets induced a significant increase on histological changes on the intestine, liver and lymphoid organs. In addition, a significant increase on lymphocyte apoptosis was observed in lymph nodes and spleen in the animals receiving the contaminated diets. These data provide a better understanding of the possible effects of Fusarium toxins, alone or in combinations on the morphology of the intestine and lymphoid organs, which would contribute to the risk assessment of these toxins.


Assuntos
Intestinos/efeitos dos fármacos , Fígado/efeitos dos fármacos , Tricotecenos/toxicidade , Zearalenona/toxicidade , Ração Animal , Animais , Proliferação de Células/efeitos dos fármacos , Interações Medicamentosas , Contaminação de Alimentos , Intestinos/patologia , Fígado/patologia , Masculino , Suínos/crescimento & desenvolvimento , Aumento de Peso/efeitos dos fármacos
2.
Br J Nutr ; 107(12): 1776-86, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21936967

RESUMO

Deoxynivalenol (DON) and fumonisins (FB) are mycotoxins produced by Fusarium species, which naturally co-occur in animal diets. The gastrointestinal tract represents the first barrier met by exogenous food/feed compounds. The purpose of the present study was to investigate the effects of DON and FB, alone and in combination, on some intestinal parameters, including morphology, histology, expression of cytokines and junction proteins. A total of twenty-four 5-week-old piglets were randomly assigned to four different groups, receiving separate diets for 5 weeks: a control diet; a diet contaminated with either DON (3 mg/kg) or FB (6 mg/kg); or both toxins. Chronic ingestion of these contaminated diets induced morphological and histological changes, as shown by the atrophy and fusion of villi, the decreased villi height and cell proliferation in the jejunum, and by the reduced number of goblet cells and lymphocytes. At the end of the experiment, the expression levels of several cytokines were measured by RT-PCR and some of them (TNF-α, IL-1ß, IFN-γ, IL-6 and IL-10) were significantly up-regulated in the ileum or the jejunum. In addition, the ingestion of contaminated diets reduced the expression of the adherent junction protein E-cadherin and the tight junction protein occludin in the intestine. When animals were fed with a co-contaminated diet (DON+FB), several types of interactions were observed depending on the parameters and segments assessed: synergistic (immune cells); additive (cytokines and junction protein expression); less than additive (histological lesions and cytokine expression); antagonistic (immune cells and cytokine expression). Taken together, the present data provide strong evidence that chronic ingestion of low doses of mycotoxins alters the intestine, and thus may predispose animals to infections by enteric pathogens.


Assuntos
Dieta , Contaminação de Alimentos , Fumonisinas/efeitos adversos , Fusarium/química , Mucosa Intestinal/efeitos dos fármacos , Intestino Delgado/efeitos dos fármacos , Tricotecenos/efeitos adversos , Animais , Caderinas/metabolismo , Citocinas/metabolismo , Células Caliciformes/efeitos dos fármacos , Infecções/etiologia , Mucosa Intestinal/imunologia , Mucosa Intestinal/patologia , Intestino Delgado/imunologia , Intestino Delgado/metabolismo , Intestino Delgado/patologia , Linfócitos/efeitos dos fármacos , Masculino , Proteínas de Membrana/metabolismo , Ocludina , Distribuição Aleatória , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Suínos , Regulação para Cima
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