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dc.contributor.authorFernánez, Ana
dc.contributor.authorPalenzuela Muñoz, Rocío 
dc.contributor.authorRuiz de Martín Esteban, Samuel 
dc.contributor.authorTorres Aleman, Ignacio
dc.date.accessioned2022-09-15T10:34:27Z
dc.date.available2022-09-15T10:34:27Z
dc.date.issued2022
dc.identifier.issn0027-8424spa
dc.identifier.urihttps://hdl.handle.net/10641/3104
dc.description.abstractCirculating insulin enters the brain through mechanisms incompletely characterized. We now report that mice lacking insulin receptors (IR) in astrocytes (GFAP-IR KO mice) show blunted brain responses to insulin, uncoupling of brain blood flow with glucose uptake with concomitant changes in brain vasculature and glucose transporter 1 levels. IR-deficient astrocytes show increased expression of HIF-1α/VEGF, promote growth of co-cultured endothelial cells, display increased reactive oxidant species (ROS) and disturbed mitochondrial activity. Treatment with the antioxidant N-acetylcysteine (NAC), ameliorated high ROS levels, normalized angiogenic signaling, and mitochondrial function including mitochondrial glucose and oxygen sensors. In vivo treatment with NAC also normalized brain perfusion. Thus, insulin receptors in astrocytes regulate neuro-vascular coupling.spa
dc.language.isoengspa
dc.publisherProceedings of the National Academy of Sciences (PNAS)spa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.titleInsulin regulates neurovascular coupling through astrocytes.spa
dc.typejournal articlespa
dc.type.hasVersionSMURspa
dc.rights.accessRightsopen accessspa
dc.description.extent4711 KBspa
dc.identifier.doi10.1073/pnas.2204527119spa
dc.relation.publisherversionhttps://www.pnas.org/doi/full/10.1073/pnas.2204527119spa


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