Bioassay-guided isolation of human carboxylesterase 2 inhibitory and antioxidant constituents from Laportea bulbifera: Inhibition interactions and molecular mechanism

• Published in: Arabian journal of chemistry 2022-04, Vol.15 (4), p.103723, Article 103723
• Main Authors: Wang, Miao-Miao, Li, Ya-Nan, Ming, Wei-Kang, Wu, Pan-Feng, Yi, Ping, Gong, Zi-Peng, Hao, Xiao-Jiang, Yuan, Chun-Mao
• Format: Article
• Language: English
• Subjects: Bioassay-guided isolation; COX-2 selective inhibitors; Enzyme kinetics; Laportea bulbifera (Sieb. et. Zucc.) Wedd; Molecular simulation; Structure-activity relationships
• ISSN: 1878-5352; 1878-5379
• DOI: 10.1016/j.arabjc.2022.103723

Laportea bulbifera (Sieb. et. Zucc.) Wedd has long been utilized in Traditional Chinese Medicines (TCM) for the treatment of rheumatoid arthritis. However, the study of systematic anti-inflammatory chemical constituents in L. bulbifera has never been reported. Thus, bioassay-guided isolation for its roots part led to 46 compounds, including 38 phenolic derivatives. Their structures were determined on the basis of 1H and 13C NMR and MS spectra. All compounds were isolated from L. bulbifera for the first time except for 13 compounds. Most of the compounds showed good COX-2 inhibitory activity (IC50: 0.13–3.94 μM) and DPPH radical-scavenging activity (IC50: 1.57–9.55 μM). Four compounds (4, 17, 35, and 43) with different skeletons showed preferential COX-2 over COX-1 inhibition with selective indices ranging from 12 to 171. High content active compounds are important for elucidating the basis of the active substance of TCM. Compound 4 (COX-2, IC50 0.24 μM), a high content compound, represented one of the best selective COX-2 inhibitors. Another high content active compound (35) with a different skeleton might have different mechanism. Further study for the inhibition kinetics against COX-2 indicated compounds 4 and 35 were noncompetitive and competitive COX-2 inhibitors, respectively. Moreover, molecular docking and molecular dynamics simulation data further indicated that compound 4 could bind in the cavity of COX-2 and interacted with key residues VAL-538, PHE-142, and GLY-225 of COX-2 through hydrogen bonds. The results indicated that L. bulbifera roots could be applied as antioxidant and anti-inflammatory agents due to their potent selective COX-2 inhibitory and antioxidant activity of phenolic compounds.