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    Por favor, use este identificador para citar o enlazar este ítem:http://uvadoc.uva.es/handle/10324/16738

    Título
    Protective effects of epoxypukalide on pancreatic b-cells and glucose metabolism in STZ-induced diabetic mice
    Autor
    López Acosta, José Francisco
    Villa Pérez, Pablo
    Fernández Díaz, Cristina MaríaAutoridad UVA Orcid
    Luis Román, Daniel Antonio deAutoridad UVA Orcid
    Díaz Marrero, Ana R.
    Cueto, Mercedes
    Perdomo Hernández, Germán
    Cózar Castellano, IreneAutoridad UVA Orcid
    Año del Documento
    2015
    Editorial
    Taylor & Francis
    Descripción
    Producción Científica
    Documento Fuente
    Islets,(2015);7(2):e1078053
    Résumé
    Diabetes is a consequence of a decrease on functional β-cell mass. We have recently demonstrated that epoxypukalide (Epoxy) is a natural compound with beneficial effects on primary cultures of rat islets. In this study, we extend our previous investigations to test the hypothesis that Epoxy protects β-cells and improves glucose metabolism in STZ-induced diabetic mice. We used 3-months old male mice that were treated with Epoxy at 200 μg/kg body weight. Glucose intolerance was induced by multiple intraperitoneal low-doses of streptozotocin (STZ) on 5 consecutive days. Glucose homeostasis was evaluated measuring plasma insulin levels and glucose tolerance. Histomorphometry was used to quantify the number of pancreatic β-cells per islet. β-cell proliferation was assessed by BrdU incorporation, and apoptosis by TUNEL staining. Epoxy treatment significantly improved glucose tolerance and plasma insulin levels. These metabolic changes were associated with increased β-cell numbers, as a result of a two-fold increase in β-cell proliferation and a 50% decrease in β-cell death. Our results demonstrate that Epoxy improves whole-body glucose homeostasis by preventing pancreatic β-cell death due to STZ-induced toxicity in STZ-treated mice
    Materias (normalizadas)
    Diabetes - Tratamiento
    ISSN
    1938-2014
    Revisión por pares
    SI
    DOI
    10.1080/19382014.2015.1078053
    Idioma
    eng
    URI
    http://uvadoc.uva.es/handle/10324/16738
    Derechos
    openAccess
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    • DEP06 - Artículos de revista [352]
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    Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepté là où spécifié autrement, la license de ce document est décrite en tant que Attribution-NonCommercial-NoDerivatives 4.0 International

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