Peroxisome proliferator-activated receptor gamma is expressed in hippocampal neurons and its activation prevents beta-amyloid neurodegeneration: role of Wnt signaling
dc.contributor.author | Inestrosa, NC | |
dc.contributor.author | Godoy, JA | |
dc.contributor.author | Quintanilla, RA | |
dc.contributor.author | Koenig, CS | |
dc.contributor.author | Bronfman, M | |
dc.date.accessioned | 2024-01-10T12:07:28Z | |
dc.date.available | 2024-01-10T12:07:28Z | |
dc.date.issued | 2005 | |
dc.description.abstract | The molecular pathogenesis of Alzheimer's disease (AD) involves the participation of the amyloid-beta-peptide (Abeta), which plays a critical role in the neurodegeneration that triggers the disease. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors, which are members of the nuclear receptor family. We report here that (1) PPARgamma is present in rat hippocampal neurons in culture. (2) Activation of PPAR-gamma by troglitazone and rosiglitazone protects rat hippocampal neurons against Abeta-induced neurodegeneration, as shown by the 3-[4,5 -2yl]-2,5-diphenyltetrazolium bromide (MTT) reduction assay, immunofluorescence using an anti-heavy neurofilament antibody, and quantitative electron microscopy. (3) Hippocampal neurons treated with several PPAR-gamma agonists, including troglitazone, rosiglitazone, and ciglitazone, prevent the excitotoxic Abeta-induced rise in bulk-free Ca2+. (4) PPARgamma activation results in the modulation of Wnt signaling components, including the inhibition of glycogen synthase kinase-3beta (GSK-3beta) and an increase of the cytoplasmic and nuclear beta-catenin levels. We conclude that the activation of PPARgamma prevents Abeta-induced neurodegeneration by a mechanism that may involve a cross talk between neuronal PPAR-y and the Writ signaling pathway. More important, the fact that the activation of PPAR-y attenuated Abeta-dependent neurodegeneration opens the possibility to fight AD from a new therapeutic perspective. (C) 2004 Published by Elsevier Inc. | |
dc.fechaingreso.objetodigital | 16-04-2024 | |
dc.format.extent | 14 páginas | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1016/j.yexcr.2004.09.032 | |
dc.identifier.eissn | 1090-2422 | |
dc.identifier.issn | 0014-4827 | |
dc.identifier.pubmedid | MEDLINE:15707577 | |
dc.identifier.uri | https://doi.org/10.1016/j.yexcr.2004.09.032 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/76288 | |
dc.identifier.wosid | WOS:000227127900009 | |
dc.information.autoruc | Ciencias Biológicas;Bronfman M;S/I;98819 | |
dc.information.autoruc | Ciencias Biológicas;Inestrosa N;S/I;99331 | |
dc.information.autoruc | Ciencias Biológicas;Konig C;S/I;48645 | |
dc.issue.numero | 1 | |
dc.language.iso | en | |
dc.nota.acceso | Contenido parcial | |
dc.pagina.final | 104 | |
dc.pagina.inicio | 91 | |
dc.publisher | ELSEVIER INC | |
dc.revista | EXPERIMENTAL CELL RESEARCH | |
dc.rights | acceso restringido | |
dc.subject | Alzheimer's disease | |
dc.subject | A beta peptide | |
dc.subject | PPAR gamma | |
dc.subject | anti-diabetic drugs | |
dc.subject | cell survival | |
dc.subject | Wnt signaling | |
dc.subject | GLYCOGEN-SYNTHASE KINASE-3-BETA | |
dc.subject | ATP CHANNEL ACTIVITY | |
dc.subject | ALZHEIMERS-DISEASE | |
dc.subject | PPAR-GAMMA | |
dc.subject | INSULIN-RESISTANCE | |
dc.subject | DIABETES-MELLITUS | |
dc.subject | KINASE | |
dc.subject | TROGLITAZONE | |
dc.subject | INHIBITION | |
dc.subject | DIFFERENTIATION | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Peroxisome proliferator-activated receptor gamma is expressed in hippocampal neurons and its activation prevents beta-amyloid neurodegeneration: role of Wnt signaling | |
dc.type | artículo | |
dc.volumen | 304 | |
sipa.codpersvinculados | 98819 | |
sipa.codpersvinculados | 99331 | |
sipa.codpersvinculados | 48645 | |
sipa.index | WOS | |
sipa.index | Scopus | |
sipa.trazabilidad | Carga SIPA;09-01-2024 |
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