Show simple item record

Authordc.contributor.authorHurley, Michael J. 
Authordc.contributor.authorDeacon, Robert M.J. 
Authordc.contributor.authorBeyer, Katrin 
Authordc.contributor.authorIoannou, Elena 
Authordc.contributor.authorIbáñez, Agustin 
Authordc.contributor.authorTeeling, Jessica L. 
Authordc.contributor.authorCogram, Patricia 
Admission datedc.date.accessioned2019-03-18T12:01:24Z
Available datedc.date.available2019-03-18T12:01:24Z
Publication datedc.date.issued2018
Cita de ítemdc.identifier.citationPharmacology and Therapeutics, Volumen 188,
Identifierdc.identifier.issn1879016X
Identifierdc.identifier.issn01637258
Identifierdc.identifier.other10.1016/j.pharmthera.2018.03.001
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/167391
Abstractdc.description.abstract© 2018 Elsevier Inc. Alzheimer's disease (AD) is a multifactorial progressive neurodegenerative disease. Despite decades of research, no disease modifying therapy is available and a change of research objectives and/or development of novel research tools may be required. Much AD research has been based on experimental models using animals with a short lifespan that have been extensively genetically manipulated and do not represent the full spectrum of late-onset AD, which make up the majority of cases. The aetiology of AD is heterogeneous and involves multiple factors associated with the late-onset of the disease like disturbances in brain insulin, oxidative stress, neuroinflammation, metabolic syndrome, retinal degeneration and sleep disturbances which are all progressive abnormalities that could account for many molecular, biochemical and histopathological lesions found in brain from patients dying from AD. This review is based on the long-lived rodent Octodon degus (degu) which is a
Lenguagedc.language.isoen
Publisherdc.publisherElsevier Inc.
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourcePharmacology and Therapeutics
Keywordsdc.subjectAlzheimer's disease
Keywordsdc.subjectDegu
Keywordsdc.subjectNeurodegeneration
Keywordsdc.subjectNeuroinflammation
Keywordsdc.subjectOctodon degus
Keywordsdc.subjectβ-Amyloid
Títulodc.titleThe long-lived Octodon degus as a rodent drug discovery model for Alzheimer's and other age-related diseases
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile