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dc.contributor.author | Ordóñez-Gutiérrez, Lara | - |
dc.contributor.author | Antón Pérez, Marta | - |
dc.contributor.author | Wandosell, Francisco | - |
dc.date.accessioned | 2016-11-15T12:41:55Z | - |
dc.date.available | 2016-11-15T12:41:55Z | - |
dc.date.issued | 2015 | - |
dc.identifier | doi: 10.1016/j.nano.2014.09.015 | - |
dc.identifier | issn: 1549-9642 | - |
dc.identifier.citation | Nanomedicine: Nanotechnology, Biology, and Medicine 11: 421- 430 (2015) | - |
dc.identifier.uri | http://hdl.handle.net/10261/140238 | - |
dc.description.abstract | © 2015 Elsevier Inc. The accumulation of extracellular amyloid-beta (Aβ) peptide and intracellular neurofibrillary tangles in the brain are two major neuropathological hallmarks of Alzheimer's disease (AD). It is thought that an equilibrium exists between Aβ in the brain and in the peripheral blood and thus, it was hypothesized that shifting this equilibrium towards the blood by enhancing peripheral clearance might reduce Aβ levels in the brain: the 'sink effect'. We tested this hypothesis by intraperitoneally injecting APP/PS1 transgenic mice with small unilamellar vesicles containing either phosphatidic acid or cardiolipin over 3. weeks. This treatment reduced significantly the amount of Aβ in the plasma and the brain levels of Aβ were lighter affected. Nevertheless, this dosing regimen did modulate tau phosphorylation and glycogen synthase kinase 3 activities in the brain, suggesting that the targeting of circulating Aβ may be therapeutically relevant in AD. | - |
dc.description.sponsorship | CIBERNED (an initiative of ISCIII) and the Plan Nacional DGCYT (SAF2009-12249-C02-01) and by an Institutional grant from the 'Fundación Areces' | - |
dc.publisher | Elsevier | - |
dc.rights | openAccess | - |
dc.subject | Alzheimer treatment | - |
dc.subject | Nanoparticles | - |
dc.subject | APP/PS1 | - |
dc.subject | Amyloid-β | - |
dc.title | Repeated intraperitoneal injections of liposomes containing phosphatidic acid and cardiolipin reduce amyloid-β levels in APP/PS1 transgenic mice | - |
dc.type | artículo | - |
dc.identifier.doi | 10.1016/j.nano.2014.09.015 | - |
dc.date.updated | 2016-11-15T12:41:55Z | - |
dc.description.version | Peer Reviewed | - |
dc.language.rfc3066 | eng | - |
dc.contributor.funder | Instituto de Salud Carlos III | - |
dc.contributor.funder | Fundación Ramón Areces | - |
dc.identifier.funder | http://dx.doi.org/10.13039/501100004587 | es_ES |
dc.identifier.funder | http://dx.doi.org/10.13039/100008054 | es_ES |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | es_ES |
item.openairetype | artículo | - |
item.grantfulltext | open | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | With Fulltext | - |
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Fichero | Descripción | Tamaño | Formato | |
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Wandosell F Repeated intraperitoneal.pdf | 912,83 kB | Adobe PDF | Visualizar/Abrir |
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