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特异性促解决脂质介质:动脉粥样硬化的潜在治疗靶点。

Specialized Proresolving Lipid Mediators: A Potential Therapeutic Target for Atherosclerosis.

机构信息

Endocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.

Escuela de Nutrición y Dietética, Facultad de Medicina, Universidad Andres Bello, Concepción 4260000, Chile.

出版信息

Int J Mol Sci. 2022 Mar 15;23(6):3133. doi: 10.3390/ijms23063133.


DOI:10.3390/ijms23063133
PMID:35328553
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8955102/
Abstract

Cardiovascular disease (CVD) is a global public health issue due to its high morbidity, mortality, and economic impact. The implementation of innovative therapeutic alternatives for CVD is urgently required. Specialized proresolving lipid mediators (SPMs) are bioactive compounds derived from ω-3 and ω-6 fatty acids, integrated into four families: Lipoxins, Resolvins, Protectins, and Maresins. SPMs have generated interest in recent years due to their ability to promote the resolution of inflammation associated with the pathogeneses of numerous illnesses, particularly CVD. Several preclinical studies in animal models have evidenced their ability to decrease the progression of atherosclerosis, intimal hyperplasia, and reperfusion injury via diverse mechanisms. Large-scale clinical trials are required to determine the effects of SPMs in humans. This review integrates the currently available knowledge of the therapeutic impact of SPMs in CVD from preclinical and clinical studies, along with the implicated molecular pathways. In vitro results have been promising, and as such, SPMs could soon represent a new therapeutic alternative for CVD.

摘要

心血管疾病 (CVD) 是一个全球性的公共卫生问题,因为它具有高发病率、高死亡率和经济影响。迫切需要实施心血管疾病的创新治疗方法。特异性促解决脂质介质 (SPM) 是源自 ω-3 和 ω-6 脂肪酸的生物活性化合物,整合到四个家族中:脂氧素、消退素、保护素和maresin。由于 SPM 具有促进与多种疾病(特别是 CVD)发病机制相关的炎症消退的能力,因此近年来引起了人们的兴趣。动物模型中的几项临床前研究已经证明,它们能够通过多种机制减少动脉粥样硬化、内膜增生和再灌注损伤的进展。需要进行大规模临床试验来确定 SPM 在人类中的作用。这篇综述综合了目前从临床前和临床研究中获得的 SPM 在 CVD 中的治疗作用的知识,以及所涉及的分子途径。体外结果很有希望,因此 SPM 可能很快成为 CVD 的一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/c93bc36033bd/ijms-23-03133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/0d5ef083fb83/ijms-23-03133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/4a2bb217c883/ijms-23-03133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/c93bc36033bd/ijms-23-03133-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/0d5ef083fb83/ijms-23-03133-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/4a2bb217c883/ijms-23-03133-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0e/8955102/c93bc36033bd/ijms-23-03133-g003.jpg

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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Inflammation Resolution: Implications for Atherosclerosis.

Circ Res. 2022-1-7

[2]
Specialized Pro-Resolving Lipid Mediators: The Future of Chronic Pain Therapy?

Int J Mol Sci. 2021-9-26

[3]
Pro-resolving lipid mediators: regulators of inflammation, metabolism and kidney function.

Nat Rev Nephrol. 2021-11

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Int J Mol Sci. 2021-4-8

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Lipoxin A4 protects against paraquat‑induced acute lung injury by inhibiting the TLR4/MyD88‑mediated activation of the NF‑κB and PI3K/AKT pathways.

Int J Mol Med. 2021-5

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Mol Med Rep. 2021-5

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Regression of human coronary artery plaque is associated with a high ratio of (18-hydroxy-eicosapentaenoic acid + resolvin E1) to leukotriene B.

FASEB J. 2021-4

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