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香豆素作为 Keap1/Nrf2/ARE 信号通路的调节剂。

Coumarins as Modulators of the Keap1/Nrf2/ARE Signaling Pathway.

机构信息

Department of Pharmacology & Toxicology, Faculty of Pharmacy, Al-Azhar University-Assiut Branch, Egypt.

Biochemistry Laboratory, Chemistry Department, Faculty of Science, Assiut University, Egypt.

出版信息

Oxid Med Cell Longev. 2020 Apr 22;2020:1675957. doi: 10.1155/2020/1675957. eCollection 2020.

Abstract

The Keap1/Nrf2/ARE system is a central defensive mechanism against oxidative stress which plays a key role in the pathogenesis and progression of many diseases. Nrf2 is a redox-sensitive transcription factor controlling a variety of downstream antioxidant and cytodefensive genes. Nrf2 has a powerful anti-inflammatory activity mediated via modulating NF-B. Therefore, pharmacological activation of Nrf2 is a promising therapeutic strategy for the treatment/prevention of several diseases that are underlined by both oxidative stress and inflammation. Coumarins are natural products with promising pharmacological activities, including antioxidant, anticancer, antimicrobial, and anti-inflammatory efficacies. Coumarins are found in many plants, fungi, and bacteria and have been widely used as complementary and alternative medicines. Some coumarins have shown an ability to activate Nrf2 signaling in different cells and animal models. The present review compiles the research findings of seventeen coumarin derivatives of plant origin (imperatorin, visnagin, urolithin B, urolithin A, scopoletin, esculin, esculetin, umbelliferone, fraxetin, fraxin, daphnetin, anomalin, wedelolactone, glycycoumarin, osthole, hydrangenol, and isoimperatorin) as antioxidant and anti-inflammatory agents, emphasizing the role of Nrf2 activation in their pharmacological activities. Additionally, molecular docking simulations were utilized to investigate the potential binding mode of these coumarins with Keap1 as a strategy to disrupt Keap1/Nrf2 protein-protein interaction and activate Nrf2 signaling.

摘要

Keap1/Nrf2/ARE 系统是一种针对氧化应激的核心防御机制,在许多疾病的发病机制和进展中起着关键作用。Nrf2 是一种氧化还原敏感的转录因子,可控制多种下游抗氧化和细胞防御基因。Nrf2 通过调节 NF-B 具有强大的抗炎活性。因此,Nrf2 的药理学激活是治疗/预防氧化应激和炎症均存在的多种疾病的有前途的治疗策略。香豆素是具有有前途的药理活性的天然产物,包括抗氧化、抗癌、抗菌和抗炎作用。香豆素存在于许多植物、真菌和细菌中,并已被广泛用作补充和替代药物。一些香豆素已显示出在不同细胞和动物模型中激活 Nrf2 信号的能力。本综述汇集了十七种植物来源的香豆素衍生物(白芷素、维斯纳苷、大黄素 B、大黄素 A、茴芹内酯、七叶苷、七叶苷酸、伞形酮、花椒素、花椒素、瑞香素、阿南霉素、wedelolactone、glycycoumarin、蛇床子素、hydrangenol 和异白芷素)作为抗氧化和抗炎剂的研究结果,强调了 Nrf2 激活在其药理活性中的作用。此外,还利用分子对接模拟研究了这些香豆素与 Keap1 的潜在结合模式,作为一种破坏 Keap1/Nrf2 蛋白-蛋白相互作用并激活 Nrf2 信号的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06b/7196981/d5bd504272c6/OMCL2020-1675957.001.jpg

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