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Phenols and terpenoids: natural products as inhibitors of NLRP3 inflammasome in cardiovascular diseases

机译:酚类和萜类化合物:作为心血管疾病中NLRP3炎症小体抑制剂的天然产物

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摘要

Inflammatory infiltration has been implicated in the pathogenesis of cardiovascular diseases (CVDs). The NLRP3 inflammasome is involved in the development of several types of CVDs, including myocardial infarction, myocardial ischemia-reperfusion damage, heart failure, atrial fibrillation, and hypertension. Inhibiting the activity of NLRP3 inflammasome can inhibit the progress of CVDs. However, there is no NLRP3 inflammasome inhibitor in clinic, and it is very important to find a safe and effective NLRP3 inhibitor. Phenols and terpenoids are naturally natural products that have many anti-inflammatory effects in CVDs by modulating the NLRP3 inflammatory pathway. Thus, 20 natural products from phenols and terpenoids for the treatment of cardiovascular disease based on the inhibition of NLRP3 inflammasome were summarized and screened. Docking results showed salvianolic acid B and ellagic acid in phenols, and oridonin and triptolide in terpenoids had a better binding activity with NLRP3, which can provide theoretical support for finding novel NLRP3 inflammasome inhibitors or lead compounds in the future.
机译:炎症浸润与心血管疾病 (CVD) 的发病机制有关。NLRP3 炎症小体参与多种类型的 CVD 的发展,包括心肌梗死、心肌缺血再灌注损伤、心力衰竭、心房颤动和高血压。抑制NLRP3炎症小体的活性可以抑制CVD的进展。然而,目前临床上还没有NLRP3炎症小体抑制剂,找到一种安全有效的NLRP3抑制剂非常重要。酚类和萜类化合物是天然产物,通过调节NLRP3炎症通路对心血管疾病具有许多抗炎作用。因此,总结筛选了20种基于抑制NLRP3炎症小体的酚类和萜类化合物治疗心血管疾病的天然产物。对接结果显示,酚类化合物中的丹酚酸B和鞣花酸,萜类化合物中的冬凌草甲素和雷公藤甲素与NLRP3具有较好的结合活性,可为今后寻找新型NLRP3炎症小体抑制剂或先导化合物提供理论支持。

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