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asperflavin,一种由海洋来源真菌 Aspergillus terreus 产生的抗炎化合物。

Asperflavin, an Anti-Inflammatory Compound Produced by a Marine-Derived Fungus, Eurotium amstelodami.

机构信息

College of Chemical and Pharmaceutical Engineering, Jilin Institute of Chemical Technology, Jilin 132022, China.

Department of Marine Life Science, Jeju National University, Jeju 690-756, Korea.

出版信息

Molecules. 2017 Oct 29;22(11):1823. doi: 10.3390/molecules22111823.

Abstract

In the present study, 16 marine-derived fungi were isolated from four types of marine materials including float, algae, animals and drift woods along with the coast of Jeju Island, Korea and evaluated for anti-inflammatory effects in lipopolysaccharide (LPS)-stimulated RAW 24.7 cells. The broth and mycelium extracts from the 16 fungi were prepared and the broth extract (BE) of (015-2) inhibited nitric oxide (NO) production in LPS-stimulated RAW 264.7 cells without cytotoxicity. By further bioassay-guided isolation, three compounds including asperflavin, neoechinulin A and preechinulin were successfully isolated from the BE of . It was revealed that asperflavin showed no cytotoxicity up to 200 μM and significantly inhibited LPS-induced NO and PGE2 production in a dose-dependent manner. In the western blot results, asperflavin suppressed only inducible NOS (iNOS), but COX-2 were slightly down-regulated. Asperflavin was also observed to inhibit the production of pro-inflammatory cytokines including TNF-α, IL-1β, and IL-6. In conclusion, this study reports a potential use of asperflavin isolated from a marine fungus, as an anti-inflammatory agent via suppression of iNOS and pro-inflammatory cytokines as well as no cytotoxicity.

摘要

在本研究中,从韩国济州岛沿海的四种海洋材料(浮标、藻类、动物和漂流木)中分离出 16 株海洋来源真菌,并对其在脂多糖 (LPS) 刺激的 RAW 24.7 细胞中的抗炎作用进行评估。从 16 株真菌中制备了培养液和菌丝体提取物,并发现(015-2)的培养液提取物(BE)在无细胞毒性的情况下抑制 LPS 刺激的 RAW 264.7 细胞中的一氧化氮(NO)产生。通过进一步的生物活性导向分离,成功地从的 BE 中分离出三种化合物,包括asperflavin、neoechinulin A 和 preechinulin。结果表明,asperflavin 在高达 200 μM 的浓度下没有细胞毒性,并以剂量依赖的方式显著抑制 LPS 诱导的 NO 和 PGE2 产生。在 Western blot 结果中,asperflavin 仅抑制诱导型一氧化氮合酶 (iNOS),但 COX-2 略有下调。asperflavin 还观察到抑制包括 TNF-α、IL-1β 和 IL-6 在内的促炎细胞因子的产生。总之,本研究报道了一种从海洋真菌中分离出的 asperflavin 作为抗炎剂的潜在用途,通过抑制 iNOS 和促炎细胞因子以及无细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9642/6150366/b5416893e0e7/molecules-22-01823-g001.jpg

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