bims-smemid Biomed News
on Stress metabolism in mitochondrial dysfunction
Issue of 2024–10–27
one paper selected by
Deepti Mudartha, The International Institute of Molecular Mechanisms and Machines



  1. Alzheimers Dement. 2024 Oct 22.
    Alzheimer's Disease Metabolomics Consortium (ADMC)
       BACKGROUND: Metabolic dysregulation is a hallmark of neurodegenerative diseases, including Alzheimer's disease (AD) and progressive supranuclear palsy (PSP). Although metabolic dysregulation is a common link between these two tauopathies, a comprehensive brain metabolic comparison of the diseases has not yet been performed.
    METHODS: We analyzed 342 postmortem brain samples from the Mayo Clinic Brain Bank and examined 658 metabolites in the cerebellar cortex and the temporal cortex between the two tauopathies.
    RESULTS: Our findings indicate that both diseases display oxidative stress associated with lipid metabolism, mitochondrial dysfunction linked to lysine metabolism, and an indication of tau-induced polyamine stress response. However, specific to AD, we detected glutathione-related neuroinflammation, deregulations of enzymes tied to purines, and cognitive deficits associated with vitamin B.
    DISCUSSION: Our findings underscore vast alterations in the brain's metabolome, illuminating shared neurodegenerative pathways and disease-specific traits in AD and PSP.
    HIGHLIGHTS: First high-throughput metabolic comparison of Alzheimer's diesease (AD) versus progressive supranuclear palsy (PSP) in brain tissue. Cerebellar cortex (CER) shows substantial AD-related metabolic changes, despite limited proteinopathy. AD impacts both CER and temporal cortex (TCX); PSP's changes are primarily in CER. AD and PSP share metabolic alterations despite major pathological differences.
    Keywords:  Alzheimer's disease; brain; cognitive deficit; metabolism; mitochondrial dysfunction; neuroinflammation; oxidative stress; progressive supranuclear palsy; tau‐mediated stress
    DOI:  https://doi.org/10.1002/alz.14249