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  2. Discovery of cyclooxygenase-2 inhibitors from Kadsura coccinea by affinity ultrafiltration mass spectrometry and the anti-inflammatory activity

Discovery of cyclooxygenase-2 inhibitors from Kadsura coccinea by affinity ultrafiltration mass spectrometry and the anti-inflammatory activity

  • Fitoterapia. 2021 Jun;151:104872. doi: 10.1016/j.fitote.2021.104872.
Xiang-Yun Zhang 1 Zi-Jiao Wei 1 Wei-Li Qiao 1 Xiao-Min Sun 1 Zhi-Ling Jin 1 Wen Gong 1 Bei-Xi Jia 2
Affiliations

Affiliations

  • 1 Department of Pharmacognosy, School of Pharmaceutical Science, Zhengzhou University, No. 100 of Science Road, Zhengzhou 450001, PR China.
  • 2 Department of Pharmacognosy, School of Pharmaceutical Science, Zhengzhou University, No. 100 of Science Road, Zhengzhou 450001, PR China. Electronic address: jiabeixi@zzu.edu.cn.
Abstract

The medicinal plant Kadsura coccinea distributing in South China, was widely used for reducing inflammation and relieving pain. Previous study in our laboratory had proved the significant therapeutic effects of K. coccinea extract on Adjuvant arthritis rats. To explore the responsible components and possible mechanisms, an AUF-HPLC-Q-TOF/ MS method was employed for screening and characterizing COX-2 ligands from K. coccinea stems for the first time. Meanwhile, the molecular docking was performed to simulate the binding modes for ligands and COX-2, the cell-free Enzyme activity assay was applied to verify the direct COX-2 inhibition of potential inhibitors, and the cell-based study on COX-2 expression was to evaluate the anti-inflammatory effect of (+)-Anwulignan. As a result, the potential COX-2 Inhibitor (+)-Anwulignan significantly suppressing COX-2 expressions in LPS signaling pathways might be a good candidate for anti-inflammation and analgesia. In conclusion, AUF mass spectrometry combining the molecular docking and bioassays in vitro was an efficient approach for discovering Enzyme inhibitors from traditional herbs.

Keywords

Affinity ultrafiltration-LC/MS; Anti-inflammation; Bioassay in vitro; COX-2 inhibitor; Kadsura coccinea; Molecular docking.

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