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动脉粥样硬化与炎症关系的研究进展。

Research Progress on the Relationship between Atherosclerosis and Inflammation.

机构信息

Laboratory Animal Center, Xuzhou Medical University, Xuzhou 221004, Jiangsu, China.

出版信息

Biomolecules. 2018 Aug 23;8(3):80. doi: 10.3390/biom8030080.

DOI:10.3390/biom8030080
PMID:30142970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6163673/
Abstract

Atherosclerosis is a chronic inflammatory disease; unstable atherosclerotic plaque rupture, vascular stenosis, or occlusion caused by platelet aggregation and thrombosis lead to acute cardiovascular disease. Atherosclerosis-related inflammation is mediated by proinflammatory cytokines, inflammatory signaling pathways, bioactive lipids, and adhesion molecules. This review discusses the effects of inflammation and the systemic inflammatory signaling pathway on atherosclerosis, the role of related signaling pathways in inflammation, the formation of atherosclerosis plaques, and the prospects of treating atherosclerosis by inhibiting inflammation.

摘要

动脉粥样硬化是一种慢性炎症性疾病;不稳定的动脉粥样硬化斑块破裂、血小板聚集和血栓形成导致血管狭窄或闭塞,进而引发急性心血管疾病。与动脉粥样硬化相关的炎症是由促炎细胞因子、炎症信号通路、生物活性脂质和黏附分子介导的。本文综述了炎症和系统性炎症信号通路对动脉粥样硬化的影响、相关信号通路在炎症、动脉粥样硬化斑块形成中的作用,以及通过抑制炎症治疗动脉粥样硬化的前景。

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本文引用的文献

1
Contribution of TLR4 signaling in intermittent hypoxia-mediated atherosclerosis progression.TLR4 信号通路在间歇性低氧介导的动脉粥样硬化进展中的作用。
J Transl Med. 2018 Apr 19;16(1):106. doi: 10.1186/s12967-018-1479-6.
2
C-Reactive Protein in Atherothrombosis and Angiogenesis.C 反应蛋白在动脉粥样血栓形成和血管生成中的作用。
Front Immunol. 2018 Mar 2;9:430. doi: 10.3389/fimmu.2018.00430. eCollection 2018.
3
Potential of anti-inflammatory agents for treatment of atherosclerosis.抗炎药物治疗动脉粥样硬化的潜力。
Exp Mol Pathol. 2018 Apr;104(2):114-124. doi: 10.1016/j.yexmp.2018.01.008. Epub 2018 Jan 31.
4
Inflammatory Biomarkers Interleukin-6 and C-Reactive Protein and Outcomes in Stable Coronary Heart Disease: Experiences From the STABILITY (Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy) Trial.在稳定性冠心病中炎症生物标志物白细胞介素-6 和 C 反应蛋白与结局:来自 STABILITY(通过起始达泊利德治疗稳定动脉粥样硬化斑块)试验的经验。
J Am Heart Assoc. 2017 Oct 24;6(10):e005077. doi: 10.1161/JAHA.116.005077.
5
A systematic comparison of clinically viable nanomedicines targeting HMG-CoA reductase in inflammatory atherosclerosis.系统比较靶向炎症性动脉粥样硬化中 HMG-CoA 还原酶的临床可行纳米药物。
J Control Release. 2017 Sep 28;262:47-57. doi: 10.1016/j.jconrel.2017.07.013. Epub 2017 Jul 9.
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Hs-CRP and all-cause, cardiovascular, and cancer mortality risk: A meta-analysis.超敏C反应蛋白与全因、心血管及癌症死亡风险:一项荟萃分析。
Atherosclerosis. 2017 Apr;259:75-82. doi: 10.1016/j.atherosclerosis.2017.02.003. Epub 2017 Feb 9.
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Cell Mol Life Sci. 2017 Jun;74(12):2263-2282. doi: 10.1007/s00018-017-2490-4. Epub 2017 Feb 28.
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Int Immunopharmacol. 2017 Jan;42:81-89. doi: 10.1016/j.intimp.2016.11.014. Epub 2016 Nov 27.
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Thromb Haemost. 2017 Jan 26;117(2):357-370. doi: 10.1160/TH16-07-0524. Epub 2016 Nov 3.
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The critical role of ABCG1 and PPARγ/LXRα signaling in TLR4 mediates inflammatory responses and lipid accumulation in vascular smooth muscle cells.ABCG1和PPARγ/LXRα信号通路在Toll样受体4(TLR4)介导的血管平滑肌细胞炎症反应和脂质积累中起关键作用。
Cell Tissue Res. 2017 Apr;368(1):145-157. doi: 10.1007/s00441-016-2518-3. Epub 2016 Nov 2.