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本文引用的文献

1
Brain Shape Changes Associated With Cerebral Atrophy in Healthy Aging and Alzheimer's Disease.健康衰老和阿尔茨海默病中与脑萎缩相关的脑形态变化
Front Mech Eng. 2021 Jul;7. doi: 10.3389/fmech.2021.705653. Epub 2021 Jul 19.
2
APOE ε2 resilience for Alzheimer's disease is mediated by plasma lipid species: Analysis of three independent cohort studies.载脂蛋白 E ε2 对阿尔茨海默病的抵抗作用是由血浆脂质种类介导的:三项独立队列研究的分析。
Alzheimers Dement. 2022 Nov;18(11):2151-2166. doi: 10.1002/alz.12538. Epub 2022 Jan 25.
3
Lipid Metabolism Influence on Neurodegenerative Disease Progression: Is the Vehicle as Important as the Cargo?脂质代谢对神经退行性疾病进展的影响:载体与所载物同样重要吗?
Front Mol Neurosci. 2021 Dec 20;14:788695. doi: 10.3389/fnmol.2021.788695. eCollection 2021.
4
Association of Lipidomics Signatures in Blood with Clinical Progression in Preclinical and Prodromal Alzheimer's Disease.血液脂质组学特征与临床前和前驱期阿尔茨海默病临床进展的关联。
J Alzheimers Dis. 2022;85(3):1115-1127. doi: 10.3233/JAD-201504.
5
The Crucial Roles of Phospholipids in Aging and Lifespan Regulation.磷脂在衰老和寿命调节中的关键作用。
Front Physiol. 2021 Nov 23;12:775648. doi: 10.3389/fphys.2021.775648. eCollection 2021.
6
Structural amyloid plaque polymorphism is associated with distinct lipid accumulations revealed by trapped ion mobility mass spectrometry imaging.结构淀粉样斑块多态性与被捕获离子淌度质谱成像显示的不同脂质蓄积相关。
J Neurochem. 2022 Feb;160(4):482-498. doi: 10.1111/jnc.15557. Epub 2021 Dec 26.
7
Modulation of Neurolipid Signaling and Specific Lipid Species in the Triple Transgenic Mouse Model of Alzheimer's Disease.阿尔茨海默病三转基因小鼠模型中神经脂质信号和特定脂质种类的调制。
Int J Mol Sci. 2021 Nov 12;22(22):12256. doi: 10.3390/ijms222212256.
8
Adult-onset CNS myelin sulfatide deficiency is sufficient to cause Alzheimer's disease-like neuroinflammation and cognitive impairment.成年期中枢神经系统硫酸脑苷脂缺乏足以导致阿尔茨海默病样神经炎症和认知障碍。
Mol Neurodegener. 2021 Sep 15;16(1):64. doi: 10.1186/s13024-021-00488-7.
9
Association of plasma and CSF cytochrome P450, soluble epoxide hydrolase, and ethanolamide metabolism with Alzheimer's disease.血浆和脑脊液细胞色素 P450、可溶性环氧化物水解酶和乙醇胺代谢与阿尔茨海默病的关系。
Alzheimers Res Ther. 2021 Sep 6;13(1):149. doi: 10.1186/s13195-021-00893-6.
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Extracellular protein components of amyloid plaques and their roles in Alzheimer's disease pathology.淀粉样斑块的细胞外蛋白成分及其在阿尔茨海默病病理中的作用。
Mol Neurodegener. 2021 Aug 28;16(1):59. doi: 10.1186/s13024-021-00465-0.

基于质谱法的脂质与阿尔茨海默病病理学关系的分析——综述

Mass Spectrometry-Based Analysis of Lipid Involvement in Alzheimer's Disease Pathology-A Review.

作者信息

Kelley Andrea R

机构信息

Department of Chemistry, United States Air Force Academy, Colorado Spring, CO 80840, USA.

出版信息

Metabolites. 2022 Jun 2;12(6):510. doi: 10.3390/metabo12060510.

DOI:10.3390/metabo12060510
PMID:35736443
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9228715/
Abstract

Irregularities in lipid metabolism have been linked to numerous neurodegenerative diseases. The roles of abnormal brain, plasma, and cerebrospinal fluid (CSF) lipid levels in Alzheimer's disease (AD) onset and progression specifically have been described to a great extent in the literature. Apparent hallmarks of AD include, but are not limited to, genetic predisposition involving the APOE Ɛ4 allele, oxidative stress, and inflammation. A common culprit tied to many of these hallmarks is disruption in brain lipid homeostasis. Therefore, it is important to understand the roles of lipids, under normal and abnormal conditions, in each process. Lipid influences in processes such as inflammation and blood-brain barrier (BBB) disturbance have been primarily studied via biochemical-based methods. There is a need, however, for studies focused on uncovering the relationship between lipid irregularities and AD by molecular-based quantitative analysis in transgenic animal models and human samples alike. In this review, mass spectrometry as it has been used as an analytical tool to address the convoluted relationships mentioned above is discussed. Additionally, molecular-based mass spectrometry strategies that should be used going forward to further relate structure and function relationships of lipid irregularities and hallmark AD pathology are outlined.

摘要

脂质代谢异常与多种神经退行性疾病有关。大脑、血浆和脑脊液(CSF)脂质水平异常在阿尔茨海默病(AD)发病和进展中的作用在文献中已有大量描述。AD的明显特征包括但不限于涉及APOE ε4等位基因的遗传易感性、氧化应激和炎症。与许多这些特征相关的一个常见罪魁祸首是脑脂质稳态的破坏。因此,了解脂质在正常和异常条件下在每个过程中的作用非常重要。脂质在炎症和血脑屏障(BBB)紊乱等过程中的影响主要通过基于生化的方法进行研究。然而,需要通过转基因动物模型和人类样本中的基于分子的定量分析来开展研究,以揭示脂质异常与AD之间的关系。在这篇综述中,将讨论质谱作为一种分析工具来解决上述复杂关系的应用。此外,还概述了未来应采用的基于分子的质谱策略,以进一步关联脂质异常与AD标志性病理的结构和功能关系。