Toxicological Assessment of [beta]-(1a6)-Glucan (Lasiodiplodan) in Mice during a 28-Day Feeding Study by Gavage

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...

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Published inMolecules (Basel, Switzerland) Vol. 17; no. 12; p. 14298
Main Authors Túrmina, Janaína A, Carraro, Emerson, da, Mario A Alves, Dekker, Robert F H, Barbosa, Aneli M, Santos, Fabio Seidel dos, Silva, Luiz A, Malfatti, Carlos R M
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 01.12.2012
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Summary: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 collected for histopathological analysis. Statistical analysis was performed through one-way analysis of variance and only p < 0.05 F-values were presented. Significant reduction in blood glucose in the male group (35%; p < 0.01), transaminases activity in both sexes (AST and ALT; ~35%; p < 0.05), and urea (20%; p < 0.01) in the female group was observed with the lasiodiplodan treatment. The results showed that sub-chronic treatments with lasiodiplodan did not generate hematological and histopathological alterations leading to signs of toxicity in healthy mice, independent of gender.
ISSN:1420-3049
DOI:10.3390/molecules171214298