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Anti-inflammatory mechanisms and research progress of colchicine in atherosclerotic therapy

机译:动脉粥样硬化疗法中血清序列的抗炎机制及研究进展

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Inflammatory responses play a vital role in the onset and development of atherosclerosis, and throughout the entire process of the chronic disease. The inflammatory responses in atherosclerosis are mainly mediated by the NLRP3 inflammasome and its downstream inflammatory factors. As a powerful anti-inflammatory medicine, colchicine has a history of more than 200?years in clinical application and is the first-choice treatment for immune diseases such as gout and familial Mediterranean fever. In atherosclerosis, colchicine can inhibit the assembly and activation of NLRP3 inflammasome via various mechanisms to effectively reduce the expression of inflammatory factors, thereby reducing the inflammation. Recent clinical trials show that a low dose of colchicine (0.5?mg per day) has a certain protective effect in stable angina patients or those with acute myocardial infarction after PCI. This article summarizes and discusses the mechanisms of colchicine in the treatment of atherosclerosis and the latest research progress.
机译:炎症反应在动脉粥样硬化的发作和发育中发挥着至关重要的作用,以及整个慢性疾病的整个过程。动脉粥样硬化中的炎症反应主要由NLRP3炎症和下游炎症因素介导。作为一种强大的抗炎医学,血清曲霉在临床应用中具有200多年的历史,是痛风和家族性地中海的免疫疾病的首选治疗。在动脉粥样硬化中,通过各种机制可以抑制组装和活化NLRP3炎性的炎性炎症,从而减少炎症因子的表达,从而减少炎症。最近的临床试验表明,低剂量的血清序列(每天0.5μmg)在稳定的心绞痛患者或PCI之后具有急性心肌梗塞的血管内患者具有一定的保护作用。本文总结并讨论了血清曲霉在治疗动脉粥样硬化和最新研究进展中的机制。

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