4.6 Article

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

Journal

INFECTION AND DRUG RESISTANCE
Volume 11, Issue -, Pages 1945-1957

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S176390

Keywords

fusidic acid; derivative; antimicrobial; anti-inflammatory

Funding

  1. National Natural Science Foundation of China [81803390]
  2. Joint Research Project of Liverpool-Guangdong Drug Discovery Initiative [607140051]
  3. Foundation of High-level Personnel Research Activation [2017RC04]
  4. Youth Innovation Talents Program of Guangdong Province [2017KQNCX200]
  5. Foundation of Department of Education of Guangdong Province [2017KQNCX200, 2016KCXTD005, 2017KSYS010]
  6. Youth Foundation of Wuyi University [2017td01]
  7. Doctor Research Activation Funding of Wuyi University [5011701521]
  8. MRC [MC_PC_17167] Funding Source: UKRI

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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. 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-beta, TNF-alpha, and COX-2. WU-FA-01 significantly suppressed the expression levels of p65, I kappa B-alpha, and p-I kappa B-alpha in the TPA-induced mouse ear model. 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.

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