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Compromised autophagy and mitophagy in brain ageing and Alzheimer's diseases

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F22%3A10457971" target="_blank" >RIV/00216208:11130/22:10457971 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/22:10457971

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Tbym.0ZDCT" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Tbym.0ZDCT</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.nbas.2022.100056" target="_blank" >10.1016/j.nbas.2022.100056</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Compromised autophagy and mitophagy in brain ageing and Alzheimer's diseases

  • Original language description

    Alzheimer&apos;s disease (AD) is one of the most persistent and devastating neurodegenerative disorders of old age, and is characterized clinically by an insidious onset and a gradual, progressive deterioration of cognitive abilities, ranging from loss of memory to impairment of judgement and reasoning. Despite years of research, an effective cure is still not available. Autophagy is the cellular &apos;garbage&apos; clearance system which plays fundamental roles in neurogenesis, neuronal development and activity, and brain health, including memory and learning. A selective sub-type of autophagy is mitophagy which recognizes and degrades damaged or superfluous mitochondria to maintain a healthy and necessary cellular mitochondrial pool. However, emerging evidence from animal models and human samples suggests an age-dependent reduction of autophagy and mitophagy, which are also compromised in AD. Upregulation of autophagy/mitophagy slows down memory loss and ameliorates clinical features in animal models of AD. In this review, we give an overview of autophagy and mitophagy and their link to the progression of AD. We also summarize approaches to upregulate autophagy/mitophagy. We hypothesize that age-dependent compromised autophagy/mitophagy is a cause of brain ageing and a risk factor for AD, while restoration of autophagy/mitophagy to more youthful levels could return the brain to health.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30103 - Neurosciences (including psychophysiology)

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Aging Brain

  • ISSN

    2589-9589

  • e-ISSN

    2589-9589

  • Volume of the periodical

    2

  • Issue of the periodical within the volume

    2022

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    19

  • Pages from-to

    100056

  • UT code for WoS article

    001134924700025

  • EID of the result in the Scopus database