4.7 Article

Novel 18β-glycyrrhetinic acid derivatives as a Two-in-One agent with potent antimicrobial and anti-inflammatory activity

期刊

BIOORGANIC CHEMISTRY
卷 122, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2022.105714

关键词

18 beta-Glycyrrhetinic acid; Oleanane derivatives; Antimicrobial; Anti-inflammatory; Mechanism

资金

  1. National Natural Science Foundation of China [81901678, 81803390, 22077020, 22077111]
  2. Natural Science Foundation of Guangdong Province [2021A1515010221]
  3. Science Foundation for Young Teachers, Wuyi University [2019td04]
  4. Special Fund Project of Science and Technology Innovation Strategy of Guangdong Province 2018 and 2020 [(2018) 352, (2020) 182]
  5. Project of Jiangmen city social welfare innovation platform construction [2016350100170008351, 2018090103460022105]
  6. Foundation of Department of Education of Guangdong Province [2020KZDZX1202, 2018KTSCX236, 2017KSYS010]
  7. Jiangmen Program for Innovative Research Team [2018630100180019806]

向作者/读者索取更多资源

This study presents the design and synthesis of a series of new derivatives of 18 beta-glycyrrhetinic acid (GA), a natural compound with antimicrobial and anti-inflammatory properties. The derivatives functionalized with a di-substituted phenyl group at the 2-position of GA showed high antimicrobial activity against Gram-positive bacteria and potent anti-inflammatory effects. In vitro and in vivo experiments revealed that these derivatives exert their anti-inflammatory activities through the regulation of inflammatory signaling pathways and cytokine expression. Therefore, GA-O-02 and GA-O-06 have great application potential as potent antimicrobial and anti-inflammatory agents.
18 beta-glycyrrhetinic acid (GA) is a well-known natural compound of oleanane-type triterpene and is found possessing antimicrobial and anti-inflammatory properties. Nonetheless, its relatively low bioactivity restricts its potential in pharmaceutical applications. To maximize the potential use of this natural herbal compound as antimicrobial and anti-inflammatory agents, the rational modification of GA to enhance its pharmacological activity with low toxicity and to understand the mechanism of action is critically essential. We reported herein the design and synthesis of a series of new GA derivatives. The antimicrobial activities of these new compounds were evaluated by inhibition zone test and minimum inhibitory concentration (MIC) assay. In addition, the anti-inflammatory activity was evaluated by LPS induced BV2 cells inflammation model and 12-O-tetradecanoyl phorbol-13-acetate (TPA) induced ear inflammation mice model. It was found that the derivatives functionalized with a di-substituted phenyl group at the 2-position of GA generally displayed high antimicrobial activity against Gram-positive bacteria (MIC down to 2.5 mu M) and potent anti-inflammatory effects (inhibition of NO production up to 55%, comparable to dexamethasone). The in vitro and in vivo results also showed that GA-O-02 and GA-O-06 exert their anti-inflammatory activities through downregulation of NO, pro-inflammatory cytokines and chemokines (IL-1 beta, IL-6, IL-12, TNF-alpha, MCP-1 and MIP-1 alpha) and upregulation of anti-inflammatory cytokines (IL 10). The anti-inflammatory mechanism may involve the inhibition of NF-kappa B, MAPKs and PI3K/Akt related inflammatory signaling pathways and activation of Nrf2/HO-1 signaling pathway. The results demonstrated that GA-O-02 and GA-O-06 possess great application potential as potent antimicrobial and anti-inflammatory agents.

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