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Stem Cell Reports ; 4(4): 605-20, 2015 Apr 14.
Artículo en Inglés | MEDLINE | ID: mdl-25801507

RESUMEN

Human embryonic stem cell (hESC)-derived pancreatic progenitor cells effectively reverse hyperglycemia in rodent models of type 1 diabetes, but their capacity to treat type 2 diabetes has not been reported. An immunodeficient model of type 2 diabetes was generated by high-fat diet (HFD) feeding in SCID-beige mice. Exposure to HFDs did not impact the maturation of macroencapsulated pancreatic progenitor cells into glucose-responsive insulin-secreting cells following transplantation, and the cell therapy improved glucose tolerance in HFD-fed transplant recipients after 24 weeks. However, since diet-induced hyperglycemia and obesity were not fully ameliorated by transplantation alone, a second cohort of HFD-fed mice was treated with pancreatic progenitor cells combined with one of three antidiabetic drugs. All combination therapies rapidly improved body weight and co-treatment with either sitagliptin or metformin improved hyperglycemia after only 12 weeks. Therefore, a stem cell-based therapy may be effective for treating type 2 diabetes, particularly in combination with antidiabetic drugs.


Asunto(s)
Diferenciación Celular , Diabetes Mellitus Tipo 2/etiología , Dieta/efectos adversos , Células Madre Embrionarias Humanas/citología , Hipoglucemiantes/farmacología , Obesidad/etiología , Páncreas/citología , Trasplante de Células Madre , Células Madre/citología , Animales , Tratamiento Basado en Trasplante de Células y Tejidos , Diabetes Mellitus Tipo 2/metabolismo , Diabetes Mellitus Tipo 2/terapia , Dieta Alta en Grasa/efectos adversos , Modelos Animales de Enfermedad , Perfilación de la Expresión Génica , Glucosa/metabolismo , Humanos , Hiperglucemia , Resistencia a la Insulina , Células Secretoras de Insulina/citología , Células Secretoras de Insulina/metabolismo , Islotes Pancreáticos/citología , Hígado/anatomía & histología , Hígado/metabolismo , Ratones , Ratones SCID , Obesidad/metabolismo , Obesidad/terapia , Tamaño de los Órganos , Fenotipo
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