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半胱氨酰白三烯在心血管疾病发病机制和进展中的作用。

Role of the Cysteinyl Leukotrienes in the Pathogenesis and Progression of Cardiovascular Diseases.

机构信息

Centro Cardiologico Monzino IRCCS, Via Carlo Parea 4, 20138 Milan, Italy.

Department of Pharmacological and Biomolecular Sciences, University of Milan, Via Giuseppe Balzaretti 9, 20133 Milan, Italy.

出版信息

Mediators Inflamm. 2017;2017:2432958. doi: 10.1155/2017/2432958. Epub 2017 Aug 28.


DOI:10.1155/2017/2432958
PMID:28932020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5592403/
Abstract

Cysteinyl leukotrienes (CysLTs) are potent lipid inflammatory mediators synthesized from arachidonic acid, through the 5-lipoxygenase (5-LO) pathway. Owing to their properties, CysLTs play a crucial role in the pathogenesis of inflammation; therefore, CysLT modifiers as synthesis inhibitors or receptor antagonists, central in asthma management, may become a potential target for the treatment of other inflammatory diseases such as the cardiovascular disorders. 5-LO pathway activation and increased expression of its mediators and receptors are found in cardiovascular diseases. Moreover, the cardioprotective effects observed by using CysLT modifiers are promising and contribute to elucidate the link between CysLTs and cardiovascular disease. The aim of this review is to summarize the state of present research about the role of the CysLTs in the pathogenesis and progression of atherosclerosis and myocardial infarction.

摘要

半胱氨酰白三烯(CysLTs)是通过 5-脂氧合酶(5-LO)途径从花生四烯酸合成的强效脂类炎症介质。由于其特性,CysLTs 在炎症发病机制中起着至关重要的作用;因此,CysLT 修饰剂作为合成抑制剂或受体拮抗剂,是哮喘管理的核心,可能成为治疗其他炎症性疾病(如心血管疾病)的潜在靶点。5-LO 途径的激活以及其介质和受体的表达增加,在心血管疾病中被发现。此外,使用 CysLT 修饰剂观察到的心脏保护作用是有希望的,并有助于阐明 CysLTs 与心血管疾病之间的联系。本综述的目的是总结目前关于 CysLTs 在动脉粥样硬化和心肌梗死发病机制和进展中的作用的研究现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb1/5592403/3709bba918a6/MI2017-2432958.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb1/5592403/cf1a7b58fcc2/MI2017-2432958.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb1/5592403/3709bba918a6/MI2017-2432958.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb1/5592403/cf1a7b58fcc2/MI2017-2432958.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deb1/5592403/3709bba918a6/MI2017-2432958.002.jpg

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[4]
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[5]
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[6]
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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]
Interactions between 5-Lipoxygenase Polymorphisms and Adipose Tissue Contents of Arachidonic and Eicosapentaenoic Acids Do Not Affect Risk of Myocardial Infarction in Middle-Aged Men and Women in a Danish Case-Cohort Study.

J Nutr. 2017-7

[2]
The leukotriene receptor antagonist montelukast and its possible role in the cardiovascular field.

Eur J Clin Pharmacol. 2017-7

[3]
Common Polymorphisms in the 5-Lipoxygenase Pathway and Risk of Incident Myocardial Infarction: A Danish Case-Cohort Study.

PLoS One. 2016-11-28

[4]
Multidrug resistance protein 1 (MRP1, ABCC1), a "multitasking" ATP-binding cassette (ABC) transporter.

J Biol Chem. 2014-10-3

[5]
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J Cell Mol Med. 2014-9

[6]
Protective effect of montelukast, a cysteinyl leukotriene receptor-1 antagonist, against intestinal ischemia-reperfusion injury in the rat.

Acta Chir Belg. 2013

[7]
Multiple-site activation of the cysteinyl leukotriene receptor 2 is required for exacerbation of ischemia/reperfusion injury.

Arterioscler Thromb Vasc Biol. 2013-11-27

[8]
Cysteinyl leukotrienes regulate endothelial cell inflammatory and proliferative signals through CysLT₂ and CysLT₁ receptors.

Sci Rep. 2013-11-20

[9]
Is GPR17 a P2Y/leukotriene receptor? examination of uracil nucleotides, nucleotide sugars, and cysteinyl leukotrienes as agonists of GPR17.

J Pharmacol Exp Ther. 2013-8-1

[10]
Identification of GPR99 protein as a potential third cysteinyl leukotriene receptor with a preference for leukotriene E4 ligand.

J Biol Chem. 2013-3-15

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