dc.creatorMizgier, María Luisa
dc.creatorCataldo, Luis R.
dc.creatorGutierrez, Juan
dc.creatorSantos, José Luis
dc.creatorCasas, Mariana
dc.creatorLlanos Vidal, Paola
dc.creatorContreras Ferrat, Ariel Eduardo
dc.creatorMoro, Cedric
dc.creatorBouzakri, Karim
dc.creatorGalgani Fuentes, José
dc.date.accessioned2019-03-18T11:56:16Z
dc.date.available2019-03-18T11:56:16Z
dc.date.created2019-03-18T11:56:16Z
dc.date.issued2017
dc.identifierJournal of Diabetes Research, Volumen 2017,
dc.identifier23146753
dc.identifier23146745
dc.identifier10.1155/2017/1328573
dc.identifierhttps://repositorio.uchile.cl/handle/2250/167049
dc.description.abstract© 2017 Maria L. Mizgier et al. Fasting to postprandial transition requires a tight adjustment of insulin secretion to its demand, so tissue (e.g., skeletal muscle) glucose supply is assured while hypo-/hyperglycemia are prevented. High muscle glucose disposal after meals is pivotal for adapting to increased glycemia and might drive insulin secretion through muscle-released factors (e.g., myokines). We hypothesized that insulin influences myokine secretion and then increases glucose-stimulated insulin secretion (GSIS). In conditioned media from human myotubes incubated with/without insulin (100 nmol/L) for 24 h, myokines were qualitatively and quantitatively characterized using an antibody-based array and ELISA-based technology, respectively. C57BL6/J mice islets and Wistar rat beta cells were incubated for 24 h with control and conditioned media from noninsulin- and insulin-treated myotubes prior to GSIS determination. Conditioned media from insulin-treated versus nontreated myotubes h
dc.languageen
dc.publisherHindawi Publishing Corporation
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceJournal of Diabetes Research
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectEndocrinology
dc.titleEffect of Human Myotubes-Derived Media on Glucose-Stimulated Insulin Secretion
dc.typeArtículos de revistas


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