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3′-异戊酰基-4′-千里光酰基贝壳杉烯酮对 PMA 刺激的 A549 人肺上皮细胞炎症反应的影响。

Effects of 3'-isovaleryl-4'-senecioylkhellactone from Thunberg on PMA-Stimulated Inflammatory Response in A549 Human Lung Epithelial Cells.

机构信息

Natural Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju 28116, Republic of Korea.

College of Pharmacy, Chungbuk National University, Cheongju 28160, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2022 Jan 28;32(1):81-90. doi: 10.4014/jmb.2107.07001.

Abstract

Thunberg (PJT) has been used in traditional medicine to treat colds, coughs, fevers, and other inflammatory diseases. The goal of this study was to investigate whether 3'-isovaleryl-4'-senecioylkhellactone (IVSK) from PJT has anti-inflammatory effects on lung epithelial cells. The anti-inflammatory effects of IVSK were evaluated using phorbol 12-myristate 13-acetate (PMA)-stimulated A549 cells and regular human lung epithelial cells as a reference. IVSK reduced the secretion of the inflammatory mediators interleukin (IL)-8 and monocyte chemoattractant protein-1 (MCP-1), and the mRNA expression of IL-6, IL-8, MCP-1, and IL-1β. Additionally, it inhibited the phosphorylation of IκB kinase (IKK), p65, Iκ-Bα, and mitogen-activated protein kinases (MAPKs) p38, JNK, and ERK in A549 cells stimulated with PMA. Moreover, the binding affinity of activator protein-1 (AP-1) and nuclear factor-κB (NF-κB) was significantly reduced in the luciferase assay, while nuclear translocation was markedly inhibited by IVSK in the immunocytochemistry. These findings indicate that IVSK can protect against inflammation through the AP-1 and NF-κB pathway and could possibly be used as a lead compound for the treatment of inflammatory lung diseases.

摘要

Thunberg(远志)在传统医学中用于治疗感冒、咳嗽、发烧和其他炎症性疾病。本研究旨在探讨 3'-异戊酰基-4'-千里光酰基贝壳杉烯酮(IVSK)是否对肺上皮细胞具有抗炎作用。使用佛波醇 12-肉豆蔻酸 13-醋酸酯(PMA)刺激的 A549 细胞和正常的人肺上皮细胞作为参照,评估了 IVSK 的抗炎作用。IVSK 降低了炎症介质白细胞介素(IL)-8 和单核细胞趋化蛋白-1(MCP-1)的分泌,以及 IL-6、IL-8、MCP-1 和 IL-1β的 mRNA 表达。此外,它还抑制了 PMA 刺激的 A549 细胞中 IκB 激酶(IKK)、p65、Iκ-Bα 和丝裂原活化蛋白激酶(MAPKs)p38、JNK 和 ERK 的磷酸化。此外,在荧光素酶测定中,AP-1 和核因子-κB(NF-κB)的结合亲和力明显降低,而 IVSK 在免疫细胞化学中明显抑制了核易位。这些发现表明,IVSK 可以通过 AP-1 和 NF-κB 途径保护免受炎症,并且可能可用作治疗炎症性肺病的先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55e/9628833/edebd00ef999/jmb-32-1-81-f1.jpg

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