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比较脑代谢组学揭示阿尔茨海默病和进行性核上性麻痹中共同和独特的代谢改变。

Comparative brain metabolomics reveals shared and distinct metabolic alterations in Alzheimer's disease and progressive supranuclear palsy.

作者信息

Batra Richa, Krumsiek Jan, Wang Xue, Allen Mariet, Blach Colette, Kastenmüller Gabi, Arnold Matthias, Ertekin-Taner Nilüfer, Kaddurah-Daouk Rima F

机构信息

Department of Physiology and Biophysics, Institute for Computational Biomedicine, Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.

Department of Quantitative Health Sciences, Mayo Clinic Florida, Jacksonville, FL, USA.

出版信息

medRxiv. 2023 Jul 27:2023.07.25.23293055. doi: 10.1101/2023.07.25.23293055.

DOI:10.1101/2023.07.25.23293055
PMID:37546878
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10402214/
Abstract

Metabolic dysregulation is a hallmark of neurodegenerative diseases, including Alzheimer's disease (AD) and progressive supranuclear palsy (PSP). While metabolic dysregulation is a common link between these two tauopathies, a comprehensive brain metabolic comparison of the diseases has not yet been performed. 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. 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. Taken together, our findings underscore vast alterations in the brain's metabolome, illuminating shared neurodegenerative pathways and disease-specific traits in AD and PSP.

摘要

代谢失调是神经退行性疾病的一个标志,包括阿尔茨海默病(AD)和进行性核上性麻痹(PSP)。虽然代谢失调是这两种tau蛋白病之间的一个共同联系,但尚未对这两种疾病进行全面的脑代谢比较。我们分析了梅奥诊所脑库的342份尸检脑样本,并检测了这两种tau蛋白病患者小脑皮质和颞叶皮质中的658种代谢物。我们的研究结果表明,这两种疾病都表现出与脂质代谢相关的氧化应激、与赖氨酸代谢相关的线粒体功能障碍,以及tau蛋白诱导的多胺应激反应迹象。然而,AD特有的表现是,我们检测到与谷胱甘肽相关的神经炎症、与嘌呤相关的酶失调,以及与维生素B相关的认知缺陷。综上所述,我们的研究结果强调了大脑代谢组的巨大变化,揭示了AD和PSP中共同的神经退行性通路和疾病特异性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/7a8809d8cc30/nihpp-2023.07.25.23293055v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/80f3575440d5/nihpp-2023.07.25.23293055v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/82666cb82c0d/nihpp-2023.07.25.23293055v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/5bcba188710f/nihpp-2023.07.25.23293055v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/7a8809d8cc30/nihpp-2023.07.25.23293055v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/80f3575440d5/nihpp-2023.07.25.23293055v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/82666cb82c0d/nihpp-2023.07.25.23293055v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/5bcba188710f/nihpp-2023.07.25.23293055v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/10402214/7a8809d8cc30/nihpp-2023.07.25.23293055v1-f0004.jpg

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