银杏黄酮苷元通过激活 Nrf2 通路抑制内皮细胞猝死改善动脉粥样硬化

IF 6.1 2区 医学 Q1 CHEMISTRY, MEDICINAL
Phytotherapy Research Pub Date : 2024-11-01 Epub Date: 2024-09-25 DOI:10.1002/ptr.8321
Xingyi Chen, Zhuan Yang, Meijuan Liao, Qing Zhao, Yuan Lu, Qin Li, Shijing Liu, Shiliang Li, Jiyu Chen, Yan He
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引用次数: 0

摘要

天然抗氧化剂已被证明能有效防治动脉粥样硬化。银杏黄酮苷元(GA)具有很强的抗氧化性,可防止内皮损伤。然而,GA 保护动脉粥样硬化的机制在很大程度上仍有待探索。本研究希望找到 GA 的抗动脉粥样硬化机制。本研究以高脂肪饮食喂养的载脂蛋白E-/-小鼠为动脉粥样硬化模型。根据以下指标评估GA对动脉粥样硬化小鼠的疗效:油红 O 染色、Masson 染色、脂质含量和细胞凋亡。透射电子显微镜、Western 印迹、免疫荧光染色和碘化丙啶染色用于分析 GA 对氧化-LDL 处理的人主动脉内皮细胞的影响。GA 通过促进 Nrf2 的核转位激活了 Nrf2,从而抑制了内皮细胞的脓毒症。GA 可防止内皮细胞脓毒症,抑制氧化应激,并可抑制以高脂肪饮食喂养的载脂蛋白E-/-小鼠动脉粥样硬化的发展。在细胞水平上,GA通过降低活性氧(ROS)水平和抑制NLRP3炎性体,抑制了ox-LDL诱导的HAECs热猝死。此外,靶向 Nrf2 的 siRNA 或 Nrf2 抑制剂 ML385 可逆转这些效应。GA能将Nrf2从Keap1的螯合中释放出来,增强Nrf2的核转位和下游抗氧化蛋白的转录,加强抗氧化防御系统,抑制氧化应激,从而防止内皮细胞脓毒症,减轻动脉粥样硬化的进展。这项研究表明,GA通过调节Keap1/Nrf2的相互作用减轻了内皮细胞的脓毒症,从而揭示了天然抗氧化剂对动脉粥样硬化具有保护作用的潜在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ginkgo Flavone Aglycone Ameliorates Atherosclerosis via Inhibiting Endothelial Pyroptosis by Activating the Nrf2 Pathway.

Natural antioxidants have been shown to be effective against atherosclerosis. Ginkgo flavone aglycone (GA) has strong antioxidant properties and can protect against endothelial damage. However, the mechanisms by which GA protects against atherosclerosis remain largely unexplored. This study hopes to find the anti-atherosclerotic mechanism of GA. ApoE-/- mice fed a high-fat diet were used for modeling atherosclerosis. The efficacy of GA on mice with atherosclerosis was evaluated based on the following indicators: Oil Red O staining, Masson staining, lipid content, and apoptosis. Transmission electron microscopy, Western blot, immunofluorescence staining, and propidium iodide staining were used to analyze the effects of GA on ox-LDL-treated human aortic endothelial cells. GA activated Nrf2 by promoting the nuclear translocation of Nrf2, thereby inhibiting endothelial pyroptosis. GA prevented endothelial pyroptosis suppressed oxidative stress, and inhibited the development of atherosclerosis in ApoE-/- mice fed high-fat diets. At the cellular level, GA suppressed ox-LDL-induced pyroptosis of HAECs by reducing reactive oxygen species (ROS) levels and inhibiting NLRP3 inflammasome. Furthermore, siRNA targeting Nrf2 or ML385, an Nrf2 inhibitor, reversed these effects. GA liberated Nrf2 from Keap1 sequestration, enhanced the nuclear translocation of Nrf2 and the transcription of downstream antioxidant proteins, reinforced the antioxidant defense system, and inhibited oxidative stress, thereby preventing endothelial cell pyroptosis, and attenuating the progression of atherosclerosis. This study indicated that GA mitigated endothelial pyroptosis by modulating Keap1/Nrf2 interactions, shedding light on the potential mechanisms underlying the protective effects of natural antioxidants against atherosclerosis.

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来源期刊
Phytotherapy Research
Phytotherapy Research 医学-药学
CiteScore
12.80
自引率
5.60%
发文量
325
审稿时长
2.6 months
期刊介绍: Phytotherapy Research is an internationally recognized pharmacological journal that serves as a trailblazing resource for biochemists, pharmacologists, and toxicologists. We strive to disseminate groundbreaking research on medicinal plants, pushing the boundaries of knowledge and understanding in this field. Our primary focus areas encompass pharmacology, toxicology, and the clinical applications of herbs and natural products in medicine. We actively encourage submissions on the effects of commonly consumed food ingredients and standardized plant extracts. We welcome a range of contributions including original research papers, review articles, and letters. By providing a platform for the latest developments and discoveries in phytotherapy, we aim to support the advancement of scientific knowledge and contribute to the improvement of modern medicine.
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