Wu Yu-Jing, Li Sin-Min, Chen Chun-Lin, Chen Zih-Rong, Chen Jih-Jung
Institute of Pharmacology, College of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
Department of Pharmacy, School of Pharmaceutical Sciences, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
Bioorg Chem. 2025 Jul 1;161:108516. doi: 10.1016/j.bioorg.2025.108516. Epub 2025 May 3.
Pogostemon cablin is a well-known Lamiaceae plant and widely utilized in Traditional Chinese Medicine (TCM) for its neuroprotective, anti-inflammatory, and anxiolytic properties. In this study, 16 known compounds (1-15 and 17) and one semi-synthesized new compound, 5-hydroxy-3-isoprenyloxy-7,3',4'-trimethoxyflavone (16), including flavonoids, pyranones, sesquiterpenes, and benzenoids, were obtained and characterized from aerial parts of P. cablin and investigated for their anti-inflammatory properties through the MAPK and NF-κB signaling pathways in LPS-induced RAW264.7 macrophages. Among the isolated compounds, rhamnazin (4), pachypodol (5), and (E)-2-methyl-6-(p-tolyl)hept-3-en-2-ol (15) exhibited potent anti-inflammatory activities in LPS-induced RAW264.7 macrophages. Rhamnazin (4) significantly modulated IκBα levels and reduced the expressions of phosphorylation of JNK and p38, indicating its effects on suppressing NF-κB activation and mitigating inflammation via MAPK signaling. Pachypodol (5) selectively inhibited iNOS and p-JNK expressions, showing specificity in its anti-inflammatory activity. (E)-2-Methyl-6-(p-tolyl)hept-3-en-2-ol (15) downregulated iNOS, p-Erk, and p-JNK expressions, demonstrating a broader inhibitory profile on pro-inflammatory mediators. Further molecular docking results demonstrated bioactive compounds 4, 5, and 15 possessed strong binding affinities with key residues, particularly Hem901, Pro344, and Glu371, consistent with their NO inhibition effects. In addition, in silico prediction of physicochemical properties confirmed favorable oral bioavailability and drug-likeness, supporting their potential as lead compounds for anti-inflammatory drug development. These findings provide comprehensive molecular insight into the anti-inflammatory effects and reveal the therapeutic potential of P. cablin constituents as natural plant-derived NF-κB and MAPK-targeting anti-inflammatory agents, offering promising candidates for managing inflammatory diseases.
广藿香是一种著名的唇形科植物,因其具有神经保护、抗炎和抗焦虑特性而在传统中药中被广泛应用。在本研究中,从广藿香地上部分获得并鉴定了16种已知化合物(1 - 15和17)以及一种半合成的新化合物5 - 羟基 - 3 - 异戊烯氧基 - 7,3',4'-三甲氧基黄酮(16),这些化合物包括黄酮类、吡喃酮类、倍半萜类和苯类化合物,并通过脂多糖诱导的RAW264.7巨噬细胞中的MAPK和NF - κB信号通路研究了它们的抗炎特性。在分离出的化合物中,鼠李秦素(4)、广藿香醇(5)和(E)-2 - 甲基 - 6 -(对甲苯基)庚 - 3 - 烯 - 2 - 醇(15)在脂多糖诱导的RAW264.7巨噬细胞中表现出强大的抗炎活性。鼠李秦素(4)显著调节IκBα水平,并降低JNK和p38磷酸化的表达,表明其通过MAPK信号通路抑制NF - κB激活和减轻炎症的作用。广藿香醇(5)选择性抑制iNOS和p - JNK的表达,显示出其抗炎活性的特异性。(E)-2 - 甲基 - 6 -(对甲苯基)庚 - 3 - 烯 - 2 - 醇(15)下调iNOS、p - Erk和p - JNK的表达,对促炎介质表现出更广泛的抑制作用。进一步的分子对接结果表明,生物活性化合物4、5和15与关键残基,特别是Hem901、Pro344和Glu371具有很强的结合亲和力,这与其对NO的抑制作用一致。此外,理化性质的计算机模拟预测证实了其良好的口服生物利用度和类药性,支持它们作为抗炎药物开发先导化合物的潜力。这些发现为抗炎作用提供了全面的分子见解,并揭示了广藿香成分作为天然植物来源的靶向NF - κB和MAPK的抗炎剂的治疗潜力,为管理炎症性疾病提供了有前景的候选药物。