<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T01:11:31Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/25696" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/25696</identifier><datestamp>2026-02-03T12:01:45Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Late-life depression is able to accelerate learning and memory impairment in a mouse model of Alzheimer´s disease</dc:title>
   <dc:creator>Vegas-Gómez, Laura</dc:creator>
   <dc:creator>López-Castillo, Inés</dc:creator>
   <dc:creator>Fernández-Valenzuela, Juan José</dc:creator>
   <dc:creator>Gutiérrez-Pérez, Antonia</dc:creator>
   <dc:creator>Moreno-González, Inés</dc:creator>
   <dc:subject>Alzheimer, enfermedad de - Congresos</dc:subject>
   <dc:subject>Depresión mental - Congresos</dc:subject>
   <dcterms:abstract>Clinical studies suggest that depression could be considered an important risk factor for the future development of cognitive impairment and Alzheimer's disease (AD). In fact, there is a strong association between late-life depression and AD. The age of AD onset has been shown to be accelerated in patients with mild cognitive impairment (MCI) with a history of depression, and women appear to be particularly more vulnerable to this condition. In addition, individuals with MCI who present depressive&#xd;
symptoms have an elevated burden of amyloid-beta (Aβ), the main toxic protein associated with Alzheimer's pathology, and a higher risk of developing AD compared to non-depressed MCI patients. Although it has been described that some transgenic models of AD can develop signs similar to depression in advanced stages, the induction of Alzheimer's pathology due to a depressive process has not been studied under experimental conditions to emulate late-life depression as a risk factor for&#xd;
AD. The objective of this study is to determine, by inducing unpredictable mild chronic stress (CUMS) in tau transgenic P301S mice, whether depression is a cause, rather than a consequence, of AD development. The results of our study indicate that the induction of CUMS in transgenic animals induces phenotypic changes related to a depressive state. Behavioral and histological studies suggest that depression-like induction can worse AD pathology. The findings generated in this project could provide evidence of depression as a risk factor for AD.</dcterms:abstract>
   <dcterms:dateAccepted>2023-01-10T11:29:28Z</dcterms:dateAccepted>
   <dcterms:available>2023-01-10T11:29:28Z</dcterms:available>
   <dcterms:created>2023-01-10T11:29:28Z</dcterms:created>
   <dcterms:issued>2022</dcterms:issued>
   <dc:type>conference output</dc:type>
   <dc:identifier>https://hdl.handle.net/10630/25696</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Cold Spring Harbor Laboratory Scientific Meeting</dc:relation>
   <dc:relation>New York (virtual)</dc:relation>
   <dc:relation>30/11/2022-03/12/2022</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
   <dc:publisher>CSHL</dc:publisher>
</qdc:qualifieddc>
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