Institute of Mongolian Medicinal Chemistry, School of Chemistry & Chemical Engineering, Inner Mongolia University, Hohhot, Inner Mongolia 010020, PR China.
International Hospital of Mongolian Medicine, Hohhot, Inner Mongolia 010021, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Nov 15;1211:123458. doi: 10.1016/j.jchromb.2022.123458. Epub 2022 Sep 21.
Ethnomedicine Eerdun Wurile (EW) can significantly promote poststroke neuro-recovery through modulation of microglia polarization. Fraction 4-6 (F4-6) isolated from EW via serial fractionation inhibits the expression of pro-inflammatory genes in LPS stimulated microglia. However, the key active molecules of F4-6 have not been identified. Herein, we identified alantolactone (Ala) and dehydrodiisoeugenol (Deh) as the active anti-inflammatory components of F4-6 by UPLC-qTof MS analysis. We confirmed that, F4-6, Ala, Deh and mixture of Ala and Deh (Mix) downregulate the expression of several pro-inflammatory genes including Ccl2, Cox2 and Il6 in LPS-treated microglia in a similar pattern. At the same time upregulate the expression of anti-inflammatory genes including Hmox1, Tgfβ, Igf1 and Creb1. Moreover, the conditioned culture media obtained from F4-6 treated microglia significantly enhanced proliferation of N2a cells, and promoted neurite outgrowth possibly through upregulation of Nefh and Dlg4. Mechanistically, F4-6 strongly downregulated the expression of NF-κB p65, while also inhibiting the nuclear translocation of p65, leading to the suppression of transcription of pro-inflammatory genes initiated by NF-κB. Collectively, our data identified and quantified the key chemicals of EW and provide insights into the optimization of the herbal composition for neuroprotection.
民族药物额尔敦-乌日勒(EW)可通过调节小胶质细胞极化显著促进中风后神经恢复。通过连续分级分离从 EW 中分离得到的 4-6 馏分(F4-6)可抑制 LPS 刺激的小胶质细胞中促炎基因的表达。然而,F4-6 的关键活性分子尚未确定。在此,我们通过 UPLC-qTof MS 分析鉴定出土木香内酯(Ala)和脱氢二异丁香酚(Deh)为 F4-6 的活性抗炎成分。我们证实 F4-6、Ala、Deh 和 Ala 和 Deh 的混合物(Mix)以相似的方式下调 LPS 处理的小胶质细胞中几种促炎基因(包括 Ccl2、Cox2 和 Il6)的表达。同时上调抗炎基因的表达,包括 Hmox1、Tgfβ、Igf1 和 Creb1。此外,F4-6 处理的小胶质细胞获得的条件培养基可显著增强 N2a 细胞的增殖,并通过上调 Nefh 和 Dlg4 促进神经突生长。从机制上讲,F4-6 强烈地下调 NF-κB p65 的表达,同时抑制 p65 的核易位,从而抑制 NF-κB 启动的促炎基因的转录。总之,我们的数据鉴定和量化了 EW 的关键化学物质,并为神经保护的草药成分优化提供了思路。