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dc.creatorAraújo, Juliana Milani-
dc.creatorBraga, Fabio Ribeiro-
dc.creatorVilela, Vinícius Longo Ribeiro-
dc.creatorSoares, Filippe Elias de Freitas-
dc.creatorFerraz, Carolina Magri-
dc.creatorBindaco, Adriano Lima Stelzer-
dc.creatorAguiar, Deivisson Ferreira-
dc.creatorCorrêa, Deborah Aparecida Negrão-
dc.creatorRodrigues, Vanessa Fernandes-
dc.creatorAraújo, Jackson Victor de-
dc.date.accessioned2022-10-19T14:42:33Z-
dc.date.available2022-10-19T14:42:33Z-
dc.date.issued2022-07-31-
dc.identifier.citationARAÚJO, J. M. et al. Evaluation of the acute oral toxicity of the fungus Duddingtonia flagrans at the gut level. Biocontrol Science and Technology, [S.l.], v. 32, n. 11, p. 1275-1284, 2022. DOI: 10.1080/09583157.2022.2104809.pt_BR
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/09583157.2022.2104809pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/55296-
dc.description.abstractThe aim of the present study was to perform the histopathological and enzymatic evaluation of the intestines of Swiss mice infected with Strongyloides venezuelensis after oral administration of the fungus Duddingtonia flagrans (AC001). Twenty mice were used, all previously dewormed and kept in individual cages with granulated feed and drinking water provided ad libitum. After this period, the animals were randomly divided into four experimental groups: Group 1 (animals infected with 700 L3 of S. venezuelensis), Group 2 (animals infected with 700 L3 of S. venezuelensis + orally treated with 500 chlamydospores and 500 conidia of AC001), Group 3 (animals not infected with L3 from S. venezuelensis + orally treated with 500 chlamydospores and 500 conidia from AC001) and Group 4, control (uninfected and untreated animals with chlamydospores and AC001 conidia). After that, all animals were euthanized and necropsied. Intestinal tissue collections were intended for histopathology and enzymatic quantification of Eosinophilic Peroxidase (EPO) and Myeloperoxidase (MPO). At the end of the trial, the results showed that there was no change and/or destruction of the intestinal microvilli in the groups (G2 and G3) that received orally chlamydospores/conidia of AC001. Oral treatments with AC001 did not induce any significant increase in EPO and MPO levels in the experimental groups (G2 and G3), when compared to the control group G4 (p < 0.05). It was concluded that the fungus D. flagrans (AC001) did not cause changes in the intestinal microvilli, nor did it interfere in the levels of EOP and MPO.pt_BR
dc.languageen_USpt_BR
dc.publisherTaylor & Francispt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceBiocontrol Science and Technologypt_BR
dc.subjectNematophagous funguspt_BR
dc.subjectMicrovillipt_BR
dc.subjectIntestinal histopathologypt_BR
dc.subjectEPOpt_BR
dc.subjectMPOpt_BR
dc.subjectEosinophilic Peroxidase (EPO)pt_BR
dc.subjectMyeloperoxidase (MPO)pt_BR
dc.titleEvaluation of the acute oral toxicity of the fungus Duddingtonia flagrans at the gut levelpt_BR
dc.typeArtigopt_BR
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