Suppr超能文献

海绵 Aaptos suberitoides 中新型萘啶的抗炎作用通过调节 MAPK 和 Nrf2 信号通路在 LPS 刺激的 RAW 264.7 巨噬细胞中的作用。

Anti-Inflammatory Effects of New Naphthyridine from Sponge Aaptos suberitoides in LPS-Stimulated RAW 264.7 Macrophages via Regulation of MAPK and Nrf2 Signaling Pathways.

机构信息

Department of Oncology, Binzhou Medical University Hospital, Binzhou, 256603, China.

Medical Research Center, Binzhou Medical University Hospital, Binzhou, 256603, China.

出版信息

Chem Biodivers. 2023 Jun;20(6):e202300410. doi: 10.1002/cbdv.202300410. Epub 2023 May 12.

Abstract

Two new naphthyridine compounds, 4-methoxycarbonyl-5-oxo-1,6-naphthyridine (1) and 5-methoxycarbonyl-4-oxo-1,6-naphthyridine (2) were obtained from the MeOH extracts of sponge Aaptos suberitoides. Their structures were determined by spectroscopic methods, including HR-ESI-MS, 1D-NMR ( H-NMR, C-NMR), 2D-NMR (COSY, HSQC, HMBC). The structure of compound 1 was further confirmed via single crystal X-ray diffraction analysis. Compound 1 was found to reduce NO production in LPS-induced RAW 264.7 macrophages with IC value of 0.15 mM. In addition, it decreased the mRNA expression levels of pro-inflammatory mediators, such as the tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β), inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX2) in LPS-induced macrophages. It also decreased the protein expression of iNOS and COX-2 in LPS-induced macrophages. Mechanistic studies further revealed that compound 1 inhibited the mitogen-activated protein kinase (MAPK), and activated the nuclear factor erythroid 2-related factor 2/heme oxygenase-1 (Nrf2/HO-1) signaling pathways in LPS-induced RAW 264.7 macrophages.

摘要

从海绵 Aaptos suberitoides 的 MeOH 提取物中获得了两种新的萘啶酮化合物,4-甲氧基羰基-5-氧代-1,6-萘啶(1)和 5-甲氧基羰基-4-氧代-1,6-萘啶(2)。通过包括高分辨电喷雾电离质谱(HR-ESI-MS)、一维 NMR(H-NMR、C-NMR)、二维 NMR(COSY、HSQC、HMBC)在内的光谱方法确定了它们的结构。通过单晶 X 射线衍射分析进一步确定了化合物 1 的结构。化合物 1 被发现可降低 LPS 诱导的 RAW 264.7 巨噬细胞中 NO 的产生,IC 值为 0.15mM。此外,它降低了 LPS 诱导的巨噬细胞中促炎介质如肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)、诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX2)的 mRNA 表达水平。它还降低了 LPS 诱导的巨噬细胞中 iNOS 和 COX-2 的蛋白表达。机制研究进一步表明,化合物 1 抑制丝裂原活化蛋白激酶(MAPK),并激活 LPS 诱导的 RAW 264.7 巨噬细胞中的核因子红细胞 2 相关因子 2/血红素加氧酶-1(Nrf2/HO-1)信号通路。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验