神经退行性疾病中的髓鞘脂质变化:髓鞘脂质变化在神经退行性疾病中的作用:景观和致病影响。

IF 5.9 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Antioxidants & redox signaling Pub Date : 2024-11-22 DOI:10.1089/ars.2024.0676
Ziying Xu, Sijia He, Mst Marium Begum, Xianlin Han
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引用次数: 0

摘要

意义重大:脂质在大脑干物质中所占比例最高(超过 50%),对大脑的完整性、能量平衡和信号调节至关重要。新的证据表明,在正常衰老过程中以及在不同形式的神经退行性疾病中,都会出现脂质谱改变和脂质代谢异常。此外,越来越多的全基因组关联研究已经验证了脂质相关通路上涉及疾病发展的新靶点。髓鞘是轴突周围的保护鞘,对神经信号的有效传递至关重要。髓鞘是富含脂质的主要部位,人们越来越认识到,髓鞘受损在各种神经退行性疾病中发挥着重要而复杂的作用,而不仅仅是神经元缺失的继发效应。最新进展:随着脂质组学领域的进展,髓鞘脂质的改变及其在导致或反映阿尔茨海默病、帕金森病、亨廷顿病、肌萎缩侧索硬化症、多发性硬化症等疾病进展方面的作用最近引起了人们的极大关注。关键问题:本综述总结了五种最常见的神经退行性疾病中髓鞘脂质改变的最新发现,并讨论了它们在疾病发病机制中的意义。未来方向:通过强调神经退行性疾病中的髓鞘脂质异常,本综述旨在鼓励进一步开展以脂质为重点的研究,并在该领域开发以脂质为导向的新治疗方法。抗氧化。Redox Signal.00, 000-000.
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Myelin Lipid Alterations in Neurodegenerative Diseases: Landscape and Pathogenic Implications.

Significance: Lipids, which constitute the highest portion (over 50%) of brain dry mass, are crucial for brain integrity, energy homeostasis, and signaling regulation. Emerging evidence revealed that lipid profile alterations and abnormal lipid metabolism occur during normal aging and in different forms of neurodegenerative diseases. Moreover, increasing genome-wide association studies have validated new targets on lipid-associated pathways involved in disease development. Myelin, the protective sheath surrounding axons, is crucial for efficient neural signaling transduction. As the primary site enriched with lipids, impairments of myelin are increasingly recognized as playing significant and complex roles in various neurodegenerative diseases, beyond simply being secondary effects of neuronal loss. Recent Advances: With advances in the lipidomics field, myelin lipid alterations and their roles in contributing to or reflecting the progression of diseases, including Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, and others, have recently caught great attention. Critical Issues: This review summarizes recent findings of myelin lipid alterations in the five most common neurodegenerative diseases and discusses their implications in disease pathogenesis. Future Directions: By highlighting myelin lipid abnormalities in neurodegenerative diseases, this review aims to encourage further research focused on lipids and the development of new lipid-oriented therapeutic approaches in this area. Antioxid. Redox Signal. 00, 000-000.

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来源期刊
Antioxidants & redox signaling
Antioxidants & redox signaling 生物-内分泌学与代谢
CiteScore
14.10
自引率
1.50%
发文量
170
审稿时长
3-6 weeks
期刊介绍: Antioxidants & Redox Signaling (ARS) is the leading peer-reviewed journal dedicated to understanding the vital impact of oxygen and oxidation-reduction (redox) processes on human health and disease. The Journal explores key issues in genetic, pharmaceutical, and nutritional redox-based therapeutics. Cutting-edge research focuses on structural biology, stem cells, regenerative medicine, epigenetics, imaging, clinical outcomes, and preventive and therapeutic nutrition, among other areas. ARS has expanded to create two unique foci within one journal: ARS Discoveries and ARS Therapeutics. ARS Discoveries (24 issues) publishes the highest-caliber breakthroughs in basic and applied research. ARS Therapeutics (12 issues) is the first publication of its kind that will help enhance the entire field of redox biology by showcasing the potential of redox sciences to change health outcomes. ARS coverage includes: -ROS/RNS as messengers -Gaseous signal transducers -Hypoxia and tissue oxygenation -microRNA -Prokaryotic systems -Lessons from plant biology
期刊最新文献
Development of Calcium-Dependent Phospholipase A2 Inhibitors to Target Cellular Senescence and Oxidative Stress in Neurodegenerative Diseases. Myelin Lipid Alterations in Neurodegenerative Diseases: Landscape and Pathogenic Implications. Adeno-Associated Virus-Mediated Dickkopf-1 Gene Transduction Reduces Silica-Induced Oxidative Stress and Silicosis in Mouse Lung. Nrf2-Dependent Adaptation to Oxidative Stress Protects Against Progression of Diabetic Nephropathy. Suppression of CDK1/Drp1-Mediated Mitochondrial Fission Attenuates Dexamethasone-Induced Extracellular Matrix Deposition in the Trabecular Meshwork.
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