Lipid Oxidation at the Crossroads: Oxidative Stress and Neurodegeneration Explored in Caenorhabditis elegans.

IF 6.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Antioxidants Pub Date : 2025-01-10 DOI:10.3390/antiox14010078
Julia Tortajada-Pérez, Andrea Del Valle Carranza, Cristina Trujillo-Del Río, Mar Collado-Pérez, José María Millán, Gema García-García, Rafael Pascual Vázquez-Manrique
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Abstract

Lipid metabolism plays a critical role in maintaining cellular integrity, especially within the nervous system, where lipids support neuronal structure, function, and synaptic plasticity. However, this essential metabolic pathway is highly susceptible to oxidative stress, which can lead to lipid peroxidation, a damaging process induced by reactive oxygen species. Lipid peroxidation generates by-products that disrupt many cellular functions, with a strong impact on proteostasis. In this review, we explore the role of lipid oxidation in protein folding and its associated pathological implications, with a particular focus on findings in neurodegeneration from Caenorhabditis elegans studies, an animal model that remains underutilized. Additionally, we highlight the effectiveness of different methodologies applied in this nematode to deepen our understanding of this intricate process. In the nervous system of any animal, including mammals and invertebrates, lipid oxidation can disturb the delicate balance of cellular homeostasis, leading to oxidative stress, the build-up of toxic by-products, and protein misfolding, key factors in neurodegenerative diseases. This disruption contributes to the pathogenesis of neurodegenerative disorders such as Alzheimer's, Parkinson's, or Huntington's disease. The findings from Caenorhabditis elegans studies offer valuable insights into these complex processes and highlight potential avenues for developing targeted therapies to mitigate neurodegenerative disease progression.

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脂质氧化在十字路口:氧化应激和神经退行性变在秀丽隐杆线虫探索。
脂质代谢在维持细胞完整性方面起着至关重要的作用,特别是在神经系统中,脂质支持神经元结构、功能和突触可塑性。然而,这一重要的代谢途径极易受到氧化应激的影响,氧化应激可导致脂质过氧化,这是一种由活性氧诱导的损伤过程。脂质过氧化产生的副产物会破坏许多细胞功能,对蛋白质停滞有强烈的影响。在这篇综述中,我们探讨了脂质氧化在蛋白质折叠中的作用及其相关的病理意义,特别关注秀丽隐杆线虫研究中神经退行性变的发现,这是一种尚未充分利用的动物模型。此外,我们强调在这种线虫中应用不同方法的有效性,以加深我们对这一复杂过程的理解。在包括哺乳动物和无脊椎动物在内的任何动物的神经系统中,脂质氧化都会破坏细胞内稳态的微妙平衡,导致氧化应激、有毒副产物的积累和蛋白质错误折叠,这些都是神经退行性疾病的关键因素。这种破坏有助于神经退行性疾病的发病机制,如阿尔茨海默病、帕金森病或亨廷顿病。秀丽隐杆线虫的研究结果为这些复杂的过程提供了有价值的见解,并强调了开发靶向治疗以减轻神经退行性疾病进展的潜在途径。
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来源期刊
Antioxidants
Antioxidants Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
10.60
自引率
11.40%
发文量
2123
审稿时长
16.3 days
期刊介绍: Antioxidants (ISSN 2076-3921), provides an advanced forum for studies related to the science and technology of antioxidants. It publishes research papers, reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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