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缩醛磷脂类似物作为血小板活化因子拮抗剂:一类潜在的新型抗炎化合物。

Plasmalogenic Lipid Analogs as Platelet-Activating Factor Antagonists: A Potential Novel Class of Anti-inflammatory Compounds.

作者信息

Rong Pu, Wang Jie-Li, Angelova Angelina, Almsherqi Zakaria A, Deng Yuru

机构信息

Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, China.

CNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, Châtenay-Malabry, France.

出版信息

Front Cell Dev Biol. 2022 Apr 12;10:859421. doi: 10.3389/fcell.2022.859421. eCollection 2022.

Abstract

Plasmalogens and Platelet-Activating Factor (PAF) are both bioactive ether phospholipids. Whereas plasmalogens are recognized for their important antioxidant function and modulatory role in cell membrane structure and dynamics, PAF is a potent pro-inflammatory lipid mediator known to have messenger functions in cell signaling and inflammatory response. The relationship between these two types of lipids has been rarely studied in terms of their metabolic interconversion and reciprocal modulation of the pro-inflammation/anti-inflammation balance. The vinyl-ether bonded plasmalogen lipid can be the lipid sources for the precursor of the biosynthesis of ether-bonded PAF. In this opinion paper, we suggest a potential role of plasmalogenic analogs of PAF as modulators and PAF antagonists (anti-PAF). We discuss that the metabolic interconversion of these two lipid kinds may be explored towards the development of efficient preventive and relief strategies against PAF-mediated pro-inflammation. We propose that plasmalogen analogs, acting as anti-PAF, may be considered as a new class of bioactive anti-inflammatory drugs. Despite of the scarcity of available experimental data, the competition between PAF and its natural plasmalogenic analogs for binding to the PAF receptor (PAF-R) can be proposed as a mechanistic model and potential therapeutic perspective against multiple inflammatory diseases ( cardiovascular and neurodegenerative disorders, diabetes, cancers, and various manifestations in coronavirus infections such as COVID-19).

摘要

缩醛磷脂和血小板活化因子(PAF)都是具有生物活性的醚磷脂。缩醛磷脂因其重要的抗氧化功能以及在细胞膜结构和动力学中的调节作用而被认可,而PAF是一种强效的促炎脂质介质,已知在细胞信号传导和炎症反应中具有信使功能。关于这两种脂质在代谢相互转化以及对促炎/抗炎平衡的相互调节方面的关系,鲜有研究。乙烯基醚键合的缩醛磷脂脂质可以作为醚键合PAF生物合成前体的脂质来源。在这篇观点论文中,我们提出PAF的缩醛磷脂类似物作为调节剂和PAF拮抗剂(抗PAF)的潜在作用。我们讨论了可以探索这两种脂质的代谢相互转化,以开发针对PAF介导的促炎反应的有效预防和缓解策略。我们提出,作为抗PAF的缩醛磷脂类似物可被视为一类新型的生物活性抗炎药物。尽管现有实验数据匮乏,但可以提出PAF与其天然缩醛磷脂类似物在与PAF受体(PAF-R)结合方面的竞争,作为针对多种炎症性疾病(心血管和神经退行性疾病、糖尿病、癌症以及冠状病毒感染如COVID-19中的各种表现)的一种机制模型和潜在治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d64/9048793/11b0dea1da10/fcell-10-859421-g001.jpg

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