The biological evaluation of fusidic acid and its hydrogenation derivative as antimicrobial and anti-inflammatory agents

夫西地酸及其氢化衍生物作为抗菌消炎剂的生物学评价

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作者:Pan-Pan Wu, Hao He, W David Hong, Tong-Rong Wu, Gui-Ying Huang, Ying-Ying Zhong, Bo-Rong Tu, Min Gao, Jun Zhou, Su-Qing Zhao, Dong-Li Li, Xue-Tao Xu, Zhao-Jun Sheng, Stephen A Ward, Paul M O'Neill, Kun Zhang

Background

Fusidic acid (FA) (WU-FA-00) is the only commercially available antimicrobial from the fusidane family that has a narrow spectrum of activity against Gram-positive bacteria.

Conclusion

Overall, our results showed that WU-FA-00 and WU-FA-01 not only had effective antimicrobial activities in vitro, especially to the Gram-positive bacteria, but also possessed strong anti-inflammatory effects in vivo. These results provide a scientific basis for developing FA derivatives as antimicrobial and anti-inflammatory agents.

Methods

Herein, the hydrogenation derivative (WU-FA-01) of FA was prepared and both compounds were examined against a panel of six bacterial strains. In addition, their anti-inflammatory properties were evaluated using a 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mouse ear edema model.

Results

The results of the antimicrobial assay revealed that both WU-FA-00 and WU-FA-01 displayed a high level of antimicrobial activity against Gram-positive strains. Moreover, killing kinetic studies were performed and the results were in accordance with the minimum inhibitory concentration and minimum bactericidal concentration results. We also demonstrated that the topical application of WU-FA-00 and WU-FA-01 effectively decreased TPA-induced ear edema in a dose-dependent manner. This inhibitory effect was associated with the inhibition of TPA-induced upregulation of proinflammatory cytokines IL-1β, TNF-α, and COX-2. WU-FA-01 significantly suppressed the expression levels of p65, IκB-α, and p-IκB-α in the TPA-induced mouse ear model.

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