• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

酰基辅酶 A β-氧化在脑代谢和神经退行性疾病中的作用。

The Role of Acyl-CoA β-Oxidation in Brain Metabolism and Neurodegenerative Diseases.

机构信息

Department of Biochemistry, Faculty of Medicine, Medical University of Gdansk, 80-211 Gdansk, Poland.

Institute of Nursing and Medical Rescue, State University of Applied Sciences in Koszalin, 75-582 Koszalin, Poland.

出版信息

Int J Mol Sci. 2023 Sep 12;24(18):13977. doi: 10.3390/ijms241813977.

DOI:10.3390/ijms241813977
PMID:37762279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10531288/
Abstract

This review highlights the complex role of fatty acid β-oxidation in brain metabolism. It demonstrates the fundamental importance of fatty acid degradation as a fuel in energy balance and as an essential component in lipid homeostasis, brain aging, and neurodegenerative disorders.

摘要

本篇综述强调了脂肪酸β-氧化在大脑代谢中的复杂作用。它展示了脂肪酸降解作为能量平衡中的燃料,以及作为脂质动态平衡、大脑衰老和神经退行性疾病的重要组成部分的基本重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/0cd87701adef/ijms-24-13977-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/a39887b4635d/ijms-24-13977-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/c986df527ecf/ijms-24-13977-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/ee9568835507/ijms-24-13977-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/7ad3a6f097b3/ijms-24-13977-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/0cd87701adef/ijms-24-13977-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/a39887b4635d/ijms-24-13977-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/c986df527ecf/ijms-24-13977-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/ee9568835507/ijms-24-13977-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/7ad3a6f097b3/ijms-24-13977-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/10531288/0cd87701adef/ijms-24-13977-g005.jpg

相似文献

1
The Role of Acyl-CoA β-Oxidation in Brain Metabolism and Neurodegenerative Diseases.酰基辅酶 A β-氧化在脑代谢和神经退行性疾病中的作用。
Int J Mol Sci. 2023 Sep 12;24(18):13977. doi: 10.3390/ijms241813977.
2
Regulation of peroxisomal lipid metabolism: the role of acyl-CoA and coenzyme A metabolizing enzymes.过氧化物酶体脂质代谢的调节:酰基辅酶 A 和辅酶 A 代谢酶的作用。
Biochimie. 2014 Mar;98:45-55. doi: 10.1016/j.biochi.2013.12.018. Epub 2014 Jan 2.
3
The peroxisomal Acyl-CoA thioesterase Pte1p from Saccharomyces cerevisiae is required for efficient degradation of short straight chain and branched chain fatty acids.来自酿酒酵母的过氧化物酶体酰基辅酶A硫酯酶Pte1p是短直链和支链脂肪酸有效降解所必需的。
J Biol Chem. 2006 Apr 28;281(17):11729-35. doi: 10.1074/jbc.M511762200. Epub 2006 Feb 20.
4
Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids.视网膜营养不良蛋白酰基辅酶A结合结构域包含蛋白5(ACBD5)的缺乏会损害极长链脂肪酸的过氧化物酶体β氧化。
J Biol Chem. 2017 Jan 13;292(2):691-705. doi: 10.1074/jbc.M116.760090. Epub 2016 Nov 29.
5
Disorders of mitochondrial fatty acyl-CoA beta-oxidation.线粒体脂肪酰辅酶Aβ氧化紊乱
J Inherit Metab Dis. 1999 Jun;22(4):442-87. doi: 10.1023/a:1005504223140.
6
Peroxisomal lipid degradation via beta- and alpha-oxidation in mammals.哺乳动物中通过β-氧化和α-氧化进行的过氧化物酶体脂质降解
Cell Biochem Biophys. 2000;32 Spring:73-87. doi: 10.1385/cbb:32:1-3:73.
7
Fatty Acid Oxidation Mediated by Acyl-CoA Synthetase Long Chain 3 Is Required for Mutant KRAS Lung Tumorigenesis.突变型KRAS肺癌发生需要由酰基辅酶A合成酶长链3介导的脂肪酸氧化。
Cell Rep. 2016 Aug 9;16(6):1614-1628. doi: 10.1016/j.celrep.2016.07.009. Epub 2016 Jul 28.
8
The Physiological and Pathological Role of Acyl-CoA Oxidation.酰基辅酶 A 氧化的生理和病理作用。
Int J Mol Sci. 2023 Oct 3;24(19):14857. doi: 10.3390/ijms241914857.
9
Long-chain acyl-CoA profiles in cultured fibroblasts from patients with defects in fatty acid oxidation.脂肪酸氧化缺陷患者培养成纤维细胞中的长链酰基辅酶A谱。
Biochem Mol Med. 1995 Jun;55(1):15-21. doi: 10.1006/bmme.1995.1026.
10
Preservation of Acyl Coenzyme A Attenuates Pathological and Metabolic Cardiac Remodeling Through Selective Lipid Trafficking.酰基辅酶 A 的保存通过选择性脂质转运减轻病理性和代谢性心脏重构。
Circulation. 2019 Jun 11;139(24):2765-2777. doi: 10.1161/CIRCULATIONAHA.119.039610. Epub 2019 Mar 26.

引用本文的文献

1
Dissecting metabolic regulation of behaviors and physiology during aging in Drosophila.剖析果蝇衰老过程中行为和生理的代谢调节。
Biogerontology. 2025 Aug 19;26(5):165. doi: 10.1007/s10522-025-10306-y.
2
The neurological pathology of peroxisomal ACBD5 deficiency - lessons from patients and mouse models.过氧化物酶体ACBD5缺乏症的神经病理学——来自患者和小鼠模型的经验教训
Front Mol Neurosci. 2025 Jul 2;18:1602343. doi: 10.3389/fnmol.2025.1602343. eCollection 2025.
3
Differential DNA methylation in blood in nuclear genes that encode mitochondrial proteins in mild cognitive impairment and Alzheimer's disease.

本文引用的文献

1
Alterations of Oligodendrocyte and Myelin Energy Metabolism in Multiple Sclerosis.多发性硬化症中少突胶质细胞和髓鞘能量代谢的改变。
Int J Mol Sci. 2023 Aug 18;24(16):12912. doi: 10.3390/ijms241612912.
2
Oligodendrocyte-derived transcellular signaling regulates axonal energy metabolism.少突胶质细胞衍生的细胞间信号调节轴突能量代谢。
Curr Opin Neurobiol. 2023 Jun;80:102722. doi: 10.1016/j.conb.2023.102722. Epub 2023 Apr 5.
3
Loss of fatty acid degradation by astrocytic mitochondria triggers neuroinflammation and neurodegeneration.
轻度认知障碍和阿尔茨海默病中编码线粒体蛋白的核基因在血液中的DNA甲基化差异。
bioRxiv. 2025 Jun 20:2025.06.16.659556. doi: 10.1101/2025.06.16.659556.
4
Impact of a Formulation Containing Chaga Extract, Coenzyme Q10, and Alpha-Lipoic Acid on Mitochondrial Dysfunction and Oxidative Stress: NMR Metabolomic Insights into Cellular Energy.含有桦褐孔菌提取物、辅酶Q10和α-硫辛酸的制剂对线粒体功能障碍和氧化应激的影响:基于核磁共振代谢组学对细胞能量的洞察
Antioxidants (Basel). 2025 Jun 18;14(6):753. doi: 10.3390/antiox14060753.
5
Mitochondria: the hidden engines of traumatic brain injury-driven neurodegeneration.线粒体:创伤性脑损伤所致神经退行性变的隐匿引擎
Front Cell Neurosci. 2025 May 9;19:1570596. doi: 10.3389/fncel.2025.1570596. eCollection 2025.
6
Dissecting Metabolic Control of Behaviors and Physiology During Aging in Drosophila.剖析果蝇衰老过程中行为和生理的代谢调控
Res Sq. 2025 May 9:rs.3.rs-6550812. doi: 10.21203/rs.3.rs-6550812/v1.
7
Region-specific neuroprotective effects of meldonium pretreatment in two models of sepsis-associated encephalopathy.米屈肼预处理在两种脓毒症相关性脑病模型中的区域特异性神经保护作用。
Front Pharmacol. 2025 Apr 30;16:1588831. doi: 10.3389/fphar.2025.1588831. eCollection 2025.
8
Energy Metabolism and Brain Aging: Strategies to Delay Neuronal Degeneration.能量代谢与脑衰老:延缓神经元变性的策略
Cell Mol Neurobiol. 2025 Apr 21;45(1):38. doi: 10.1007/s10571-025-01555-z.
9
The integrated analysis of transcriptomics and metabolomics reveals the effects of tea polyphenols on lipid metabolism in lion-head geese.转录组学和代谢组学的综合分析揭示了茶多酚对狮头鹅脂质代谢的影响。
Poult Sci. 2025 Mar 1;104(6):104958. doi: 10.1016/j.psj.2025.104958.
10
Lipid metabolism, remodelling and intercellular transfer in the CNS.中枢神经系统中的脂质代谢、重塑及细胞间转运
Nat Rev Neurosci. 2025 Apr;26(4):214-231. doi: 10.1038/s41583-025-00908-3. Epub 2025 Feb 19.
星形胶质细胞线粒体中脂肪酸降解的丧失引发神经炎症和神经退行性变。
Nat Metab. 2023 Mar;5(3):445-465. doi: 10.1038/s42255-023-00756-4. Epub 2023 Mar 23.
4
Astrocytic OxPhos: more than just energy production.星形胶质细胞的氧化磷酸化:不止于能量产生。
Nat Metab. 2023 Mar;5(3):362-363. doi: 10.1038/s42255-023-00755-5.
5
Fatty acids derived from the probiotic Lacticaseibacillus rhamnosus HA-114 suppress age-dependent neurodegeneration.来源于益生菌鼠李糖乳杆菌 HA-114 的脂肪酸可抑制与年龄相关的神经退行性病变。
Commun Biol. 2022 Dec 7;5(1):1340. doi: 10.1038/s42003-022-04295-8.
6
Mitochondrial dysfunction in microglia: a novel perspective for pathogenesis of Alzheimer's disease.小胶质细胞中线粒体功能障碍:阿尔茨海默病发病机制的新视角。
J Neuroinflammation. 2022 Oct 6;19(1):248. doi: 10.1186/s12974-022-02613-9.
7
Brain Energy Metabolism: Astrocytes in Neurodegenerative Diseases.脑能量代谢:神经退行性疾病中的星形胶质细胞。
CNS Neurosci Ther. 2023 Jan;29(1):24-36. doi: 10.1111/cns.13982. Epub 2022 Oct 3.
8
Mitochondrial dysfunction is a key pathological driver of early stage Parkinson's.线粒体功能障碍是帕金森病早期的关键病理驱动因素。
Acta Neuropathol Commun. 2022 Sep 8;10(1):134. doi: 10.1186/s40478-022-01424-6.
9
Lipid metabolism and storage in neuroglia: role in brain development and neurodegenerative diseases.神经胶质细胞中的脂质代谢与储存:在脑发育和神经退行性疾病中的作用
Cell Biosci. 2022 Jul 12;12(1):106. doi: 10.1186/s13578-022-00828-0.
10
The Reversible Carnitine Palmitoyltransferase 1 Inhibitor (Teglicar) Ameliorates the Neurodegenerative Phenotype in a Drosophila Huntington's Disease Model by Acting on the Expression of Carnitine-Related Genes.肉碱棕榈酰转移酶 1 抑制剂(替格列净)通过作用于肉碱相关基因的表达改善果蝇亨廷顿病模型的神经退行性表型。
Molecules. 2022 May 13;27(10):3125. doi: 10.3390/molecules27103125.