Toxicological Assessment of β-(1à6)-Glucan (Lasiodiplodan) in Mice during a 28-Day Feeding Study by Gavage 英文参考文献.docVIP
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Toxicological Assessment of β-(1à6)-Glucan (Lasiodiplodan) in Mice during a 28-Day Feeding Study by Gavage 英文参考文献
Molecules 2012, 17, 14298-14309; doi:10.3390/molecules171214298
OPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Toxicological Assessment of β-(1?6)-Glucan (Lasiodiplodan) in
Mice during a 28-Day Feeding Study by Gavage
Janaína A. Túrmina 1, Emerson Carraro 1, Mário A. Alves da Cunha 2, Robert F. H. Dekker 3,
Aneli M. Barbosa 3, Fábio Seidel dos Santos 1, Luiz A. Silva 1 and Carlos R. M. Malfatti 1,*
1
Pharmaceutical Science and Biodiversity Postgraduate Programs, Midwest State University,
Campus CEDETEG, Guarapuava, PR, 85040-080, Brazil;
E-Mails: janainaangela@ (J.A.T.); emersoncarraro@.br (E.C.);
fabio_seidel@ (F.S.S.); luizbiologia@ (L.A.S.)
2
Department of Chemistry, Federal Technological University of Parana, Pato Branco, PR,
85503-390, Brazil, E-Mail: mcunha@.br
3
Biorefining Research Institute, Lakehead University, Thunder Bay, ON P7B 5E1, Canada;
E-Mails: rdekker@lakeheadu.ca (R.F.H.D.); anelibarbosa@ (A.M.B.)
* Author to whom correspondence should be addressed; E-Mail: crmalfatti@;
Tel.: +55-42-3621-1000; Fax: +55-42-3629-8165.
Received: 29 September 2012; in revised form: 19 November 2012 / Accepted: 20 November 2012 /
Published: 3 December 2012
Abstract: Studies evaluating the toxicity caused by fungal exopolysaccharides of the
β-(1?6)-D-glucan type are rare. In this study, the toxicological effects of sub-chronic
treatments with lasiodiplodan (β-(1?6)-D-glucan from Lasiodiplodia theobromae MMPI)
were evaluated in mice through the assessment of biochemical, hematological, and
histopathological alterations. Thirty-two mice (16 male, 16 female) were used in this study
divided in two groups; one group received lasiodiplodan (50 mg/kg body weight) daily for
28 days via gavage, and another (control group) received saline during the same period.
Blood samples were collected via cardiac puncture for hematological and biochemical
analyses. Liver, heart, kidney, and spleen were colle
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