Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
Department of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai, 200003, People's Republic of China.
Drug Des Devel Ther. 2021 Jul 20;15:3193-3206. doi: 10.2147/DDDT.S316701. eCollection 2021.
() is a cruciferous herb that is widely distributed in China, and its roots and leaves have been used in two renowned antipyretic detoxicate crude drugs in Chinese Pharmacopoeia, () and () . However, the pharmacodynamic material basis and underlying mechanisms of the herbal efficacy remained to be elucidated.
Ultra-performance liquid chromatography-quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was adopted for the chemical profiling of and . The active ingredients were screened out through the prediction of gastrointestinal absorption and druglikeness analysis using SwissADME. A herb-ingredient-target network was constructed through target prediction of the herbal active ingredients and anti-inflammation or anti-viral properties, followed by protein-protein interaction analysis. Then, the potential relevant signaling pathways were predicted by pathway enrichment. Finally, for verification, RAW 264.7 cell line was adopted to examine the anti-inflammatory and anti-viral activities of 6 representative ingredients in .
Seventy-three compounds have been identified from through UPLC-Q-TOF-MS. A total of 17 potential active ingredients were screened through pharmacokinetics and drug-likeness evaluation using SwissADME. It was shown that key targets might include TNF, AKT1, SRC, IL2, CASP9, and CASP3 in our herb-ingredient-target network, and isovitexin, a flavonoid, tended to participate in the inflammatory response, indoles were more likely to affect the cell proliferation processes, and lignans might have a broader affinity to key targets than the other active ingredients, such as regulating immune system (targeting IL-2) and PI3K-Akt signaling pathway. In vitro, indigo and secoisolariciresinol diglucoside markedly reduced TNF-α expression in Poly (I: C)-incubated cells. Isovitexin significantly inhibited TNF-α expression, and isatin treatment markedly reduced IL-1β expression in LPS-incubated cells.
As the pharmacodynamics material basis of , indoles, lignans, and flavonoids are believed to confer beneficial properties through various cellular aspects with multiple signaling pathways involved.
()是一种十字花科草本植物,在中国广泛分布,其根和叶已被用于中国药典中的两种著名的解热解毒生药()和()中。然而,草药功效的药效物质基础和作用机制仍有待阐明。
采用超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF-MS)对()和()进行化学成分分析。通过使用 SwissADME 预测胃肠道吸收和类药性,筛选出活性成分。通过预测草药活性成分的抗炎或抗病毒特性,构建草药-成分-靶标网络,然后进行蛋白质-蛋白质相互作用分析。然后,通过通路富集预测潜在的相关信号通路。最后,为了验证,采用 RAW 264.7 细胞系检测()中 6 种代表性成分的抗炎和抗病毒活性。
通过 UPLC-Q-TOF-MS 从()中鉴定出 73 种化合物。通过使用 SwissADME 进行药代动力学和类药性评价,筛选出 17 种潜在的活性成分。结果表明,我们的草药-成分-靶标网络中的关键靶标可能包括 TNF、AKT1、SRC、IL2、CASP9 和 CASP3,而类黄酮中的异荭草素倾向于参与炎症反应,吲哚类化合物更可能影响细胞增殖过程,木脂素类化合物比其他活性成分(如调节免疫系统(针对 IL-2)和 PI3K-Akt 信号通路)对关键靶标具有更广泛的亲和力。在体外,靛蓝和松脂素二葡萄糖苷显著降低 Poly(I:C)孵育细胞中 TNF-α的表达。异荭草素显著抑制 TNF-α的表达,而色氨酸处理可显著降低 LPS 孵育细胞中 IL-1β的表达。
作为()的药效物质基础,吲哚类、木脂素类和黄酮类化合物通过涉及多种信号通路的各种细胞方面发挥有益作用。