Department of Oncology, Binzhou Medical University Hospital, Binzhou, 256603, China.
Medical Research Center, Binzhou Medical University Hospital, Binzhou, 256603, China.
Chem Biodivers. 2023 Jun;20(6):e202300410. doi: 10.1002/cbdv.202300410. Epub 2023 May 12.
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.
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。