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脂肪酸:神经退行性疾病发病机制及治疗潜力的深入了解。

Fatty Acids: An Insight into the Pathogenesis of Neurodegenerative Diseases and Therapeutic Potential.

机构信息

Departamento de Nutrición y Bioquímica, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogota 110231, Colombia.

Division of Neuropharmacology and Neurologic Diseases, Yerkes National Primate Research Center, Atlanta, GA 30329, USA.

出版信息

Int J Mol Sci. 2022 Feb 25;23(5):2577. doi: 10.3390/ijms23052577.

DOI:10.3390/ijms23052577
PMID:35269720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8910658/
Abstract

One of the most common lipids in the human body is palmitic acid (PA), a saturated fatty acid with essential functions in brain cells. PA is used by cells as an energy source, besides being a precursor of signaling molecules and protein tilting across the membrane. Although PA plays physiological functions in the brain, its excessive accumulation leads to detrimental effects on brain cells, causing lipotoxicity. This mechanism involves the activation of toll-like receptors (TLR) and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathways, with the consequent release of pro-inflammatory cytokines, increased production of reactive oxygen species (ROS), endoplasmic reticulum (ER) stress, and autophagy impairment. Importantly, some of the cellular changes induced by PA lead to an augmented susceptibility to the development of Alzheimer's and Parkinson´s diseases. Considering the complexity of the response to PA and the intrinsic differences of the brain, in this review, we provide an overview of the molecular and cellular effects of PA on different brain cells and their possible relationships with neurodegenerative diseases (NDs). Furthermore, we propose the use of other fatty acids, such as oleic acid or linoleic acid, as potential therapeutic approaches against NDs, as these fatty acids can counteract PA's negative effects on cells.

摘要

人体内最常见的脂质之一是棕榈酸(PA),它是一种饱和脂肪酸,在脑细胞中具有重要的功能。PA 不仅是信号分子和跨膜蛋白倾斜的前体,还被细胞用作能量来源。尽管 PA 在大脑中发挥着生理功能,但它的过度积累会对脑细胞造成有害影响,导致脂肪毒性。这种机制涉及 toll 样受体 (TLR) 和核因子 kappa-轻链增强子的激活 B 细胞 (NF-κB) 途径,随之而来的是促炎细胞因子的释放、活性氧 (ROS) 的产生增加、内质网 (ER) 应激和自噬受损。重要的是,PA 诱导的一些细胞变化导致阿尔茨海默病和帕金森病发展的易感性增加。考虑到对 PA 的反应的复杂性和大脑的内在差异,在这篇综述中,我们概述了 PA 对不同脑细胞的分子和细胞效应及其与神经退行性疾病 (NDs) 的可能关系。此外,我们提出使用其他脂肪酸,如油酸或亚油酸,作为治疗 NDs 的潜在方法,因为这些脂肪酸可以抵消 PA 对细胞的负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/00ba47c40dcb/ijms-23-02577-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/c626c091351e/ijms-23-02577-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/e48955d45d18/ijms-23-02577-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/00ba47c40dcb/ijms-23-02577-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/c626c091351e/ijms-23-02577-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/e48955d45d18/ijms-23-02577-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0f/8910658/00ba47c40dcb/ijms-23-02577-g003.jpg

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