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Tolerability assessment of a lectin fraction from Tepary bean seeds (Phaseolus acutifolius) orally administered to rats

Our previous studies have shown that a lectin rich fraction (TBLF) extracted from Tepary bean seeds differentially inhibits cancer cells proliferation in vitro. Before testing the in vivo anticancer effect, the acute and subchronic toxicological assays in rats were conducted, where an oral dose of 5...

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Detalles Bibliográficos
Autores principales: Ferriz-Martínez, Roberto, García-García, Karina, Torres-Arteaga, Iovanna, Rodriguez-Mendez, Adriana Jheny, Guerrero-Carrillo, María de Jesús, Moreno-Celis, Ulisses, Ángeles-Zaragoza, Marco Vinicio, Blanco-Labra, Alejandro, Gallegos-Corona, Marco Alonso, Robles-Álvarez, Juan Pablo, Mendiola-Olaya, Elizabeth, Andrade-Montemayor, Héctor Mario, Garcia, Olga Patricia, Garcia-Gasca, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598141/
https://www.ncbi.nlm.nih.gov/pubmed/28962338
http://dx.doi.org/10.1016/j.toxrep.2014.10.015
Descripción
Sumario:Our previous studies have shown that a lectin rich fraction (TBLF) extracted from Tepary bean seeds differentially inhibits cancer cells proliferation in vitro. Before testing the in vivo anticancer effect, the acute and subchronic toxicological assays in rats were conducted, where an oral dose of 50 mg/body weight kg was determined as the NOAEL. This study evaluated the resistance to digestion and complete blood count (CBC) after 24 h of the orally administered 50 mg/kg TBLF. The digestion resistance test showed lectins activity retention after 72 h and the CBC study showed a high level of eosinophils, suggesting an allergic-like response. Tolerability was assayed after 6 weeks of treatment by dosing with an intragastric cannula every third day per week. It was observed a transient reduction in food intake and body weight in the first weeks, resulting in body weight gain reduction of 10% respect to the control group at the end of the study. Additionally, organs weight, histopathological analysis and blood markers for nutritional status and for liver, pancreas and renal function were not affected. Our results suggest that 50 mg/kg TBLF administered by oral route, exhibit no toxicity in rats and it was well tolerated. Further studies will focus on long-term studies.