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从青霉 TJ507 中发现具有抗神经炎症活性的含有麦角甾醇的 23,24-二醇。

Discovery of 23,24-diols containing ergosterols with anti-neuroinflammatory activity from Penicillium citrinum TJ507.

机构信息

Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, People's Republic of China.

State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Life Sciences, Hubei University, 430062, People's Republic of China.

出版信息

Bioorg Chem. 2024 Sep;150:107575. doi: 10.1016/j.bioorg.2024.107575. Epub 2024 Jun 17.

Abstract

Citristerones A-E (1-5), five new 23,24-diols containing ergosterols, along with three known analogues, were isolated from the endophytic fungus Penicillium citrinum TJ507 obtained from Hypericum wilsonii N. Robson. Their structures and absolute configurations were determined by NMR, HRESIMS, Snatzke's method, X-ray diffraction analyses and ECD calculation. Subsequently, the anti-neuroinflammatory effects of these isolates were screened using lipopolysaccharide (LPS)-induced BV-2 microglial cells, and citristerone B (2) showed outstanding anti-neuroinflammatory activity, with IC value of 0.60 ± 0.04 μM. Moreover, immunofluorescence and western blot analysis suggested that citristerone B not only reduced the release of nitric oxide (NO) and proinflammatory cytokines in LPS-induced BV-2 microglial cells, but also significantly inhibited the expression of TNF-α, iNOS and NF-κB, along with the production of cellular ROS.

摘要

Citristerones A-E(1-5),五种新的 23,24-二醇,含有麦角甾醇,以及三种已知的类似物,从内生真菌青霉 TJ507 中分离出来,TJ507 从金丝桃属植物威尔逊获得。通过 NMR、HRESIMS、Snatzke 法、X 射线衍射分析和 ECD 计算确定了它们的结构和绝对构型。随后,用脂多糖(LPS)诱导的 BV-2 小胶质细胞筛选这些分离物的抗神经炎症活性,结果表明,Citristerone B(2)具有出色的抗神经炎症活性,IC 值为 0.60±0.04 μM。此外,免疫荧光和 Western blot 分析表明,Citristerone B 不仅降低了 LPS 诱导的 BV-2 小胶质细胞中一氧化氮(NO)和促炎细胞因子的释放,还显著抑制了 TNF-α、iNOS 和 NF-κB 的表达,以及细胞 ROS 的产生。

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