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从白及块茎中分离得到的新型菲并[9,10-bc]二苯并[a,g]菲/联苯三甲醚二聚体通过抑制 NF-κB 信号通路来减轻神经炎症。

Novel phenanthrene/bibenzyl trimers from the tubers of Bletilla striata attenuate neuroinflammation via inhibition of NF-κB signaling pathway.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

出版信息

Chin J Nat Med. 2024 May;22(5):441-454. doi: 10.1016/S1875-5364(24)60641-2.

Abstract

Five novel (9,10-dihydro) phenanthrene and bibenzyl trimers, as well as two previously identified biphenanthrenes and bibenzyls, were isolated from the tubers of Bletilla striata. Their structures were elucidated through comprehensive analyses of NMR and HRESIMS spectroscopic data. The absolute configurations of these compounds were determined by calculating rotational energy barriers and comparison of experimental and calculated ECD curves. Compounds 5b and 6 exhibited inhibitory effects on LPS-induced NO production in BV-2 cells, with IC values of 12.59 ± 0.40 and 15.59 ± 0.83 μmol·L, respectively. A mechanistic study suggested that these compounds may attenuate neuroinflammation by reducing the activation of the AKT/IκB/NF-κB signaling pathway. Additionally, compounds 3a, 6, and 7 demonstrated significant PTP1B inhibitory activities, with IC values of 1.52 ± 0.34, 1.39 ± 0.11, and 1.78 ± 0.01 μmol·L, respectively. Further investigation revealed that compound 3a might inhibit LPS-induced PTP1B overexpression and NF-κB activation, thereby mitigating the neuroinflammatory response in BV-2 cells.

摘要

从白及块茎中分离得到了 5 个新的(9,10-二氢)菲并苯和二苄基三聚体,以及 2 个先前鉴定的联菲并苯和二苄基。通过全面分析 NMR 和 HRESIMS 光谱数据,阐明了它们的结构。通过计算旋转能垒和比较实验和计算的 ECD 曲线,确定了这些化合物的绝对构型。化合物 5b 和 6 对 LPS 诱导的 BV-2 细胞中 NO 生成具有抑制作用,IC 值分别为 12.59±0.40 和 15.59±0.83μmol·L。机制研究表明,这些化合物可能通过降低 AKT/IκB/NF-κB 信号通路的激活来减轻神经炎症。此外,化合物 3a、6 和 7 对 PTP1B 表现出显著的抑制活性,IC 值分别为 1.52±0.34、1.39±0.11 和 1.78±0.01μmol·L。进一步的研究表明,化合物 3a 可能通过抑制 LPS 诱导的 PTP1B 过表达和 NF-κB 激活来减轻 BV-2 细胞中的神经炎症反应。

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