Number of the records: 1  

Age-related metabolic and neurodegenerative changes in SAMP8 mice

  1. 1.
    SYSNO ASEP0563881
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAge-related metabolic and neurodegenerative changes in SAMP8 mice
    Author(s) Pačesová, A. (CZ)
    Holubová, M. (CZ)
    Hrubá, L. (CZ)
    Strnadová, V. (CZ)
    Neprašová, B. (CZ)
    Pelantová, H. (CZ)
    Kuzma, M. (CZ)
    Železná, B. (CZ)
    Kuneš, Jaroslav (FGU-C) RID, ORCID
    Maletínská, L. (CZ)
    Source TitleAging. - : Impact Journals LLC - ISSN 1945-4589
    Roč. 14, č. 18 (2022), s. 7300-7327
    Number of pages28 s.
    Languageeng - English
    CountryUS - United States
    KeywordsAlzheimer’s disease ; senescence accelerated mouse prone 8 ; neuroinflammation ; tau pathology ; insulin resistance
    OECD categoryPhysiology (including cytology)
    R&D ProjectsGA20-00546S GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportFGU-C - RVO:67985823
    UT WOS000876483400008
    EID SCOPUS85139572689
    DOI10.18632/aging.204284
    AnnotationThe most important risk factor for the development of sporadic Alzheimer's disease (AD) is ageing. Senescence accelerated mouse prone 8 (SAMP8) is a model of sporadic AD, with senescence accelerated resistant mouse (SAMR1) as a control. In this study, we aimed to determine the onset of senescence-induced neurodegeneration and the related potential therapeutic window using behavioral experiments, immunohistochemistry and western blotting in SAMP8 and SAMR1 mice at 3, 6 and 9 months of age. The Y-maze revealed significantly impaired working spatial memory of SAMP8 mice from the 6th month. With ageing, increasing plasma concentrations of proinflammatory cytokines in SAMP8 mice were detected as well as significantly increased astrocytosis in the cortex and microgliosis in the brainstem. Moreover, from the 3rd month, SAMP8 mice displayed a decreased number of neurons and neurogenesis in the hippocampus. From the 6th month, increased pathological phosphorylation of tau protein at Thr231 and Ser214 was observed in the hippocampi of SAMP8 mice. In conclusion, changes specific for neurodegenerative processes were observed between the 3rd and 6th month of age in SAMP8 mice, thus, potential neuroprotective interventions could be applied between these ages.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2023
    Electronic addresshttps://doi.org/10.18632/aging.204284
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.