JAC Advance Access published online on June 9, 2004
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh287
© 2004 by The British Society for Antimicrobial Chemotherapy
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1 Institute of Medical Microbiology and Virology, University Hospital Schleswig-Holstein, Campus Kiel, Brunswiker Str. 4, 24105 Kiel, Germany
* To whom correspondence should be addressed. E-mail: r.krausse{at}medmicrobio.uni-kiel.de.
Objectives: To investigate the in vitro activity of Extractum liquiritiae (EL), glycyrrhizic acid (GL), glycyrrhetinic acid (GA) and a novel lipophilic derivative of glycyrrhetinic acid monoglucuronide (GAMG), acetylated GAMG (aGAMG), against 29 Helicobacter pylori strains. Methods: The MIC of each compound was determined by the agar dilution method, and the killing kinetics were monitored in brain heart infusion broth ( Results: GA was the most potent compound (MIC50 /90, 50/100 mg/L), inhibiting 79.3% of the strains at MIC Conclusions: The potent in vitro activity of GA against H. pylori provides a further explanation for its beneficial effect on peptic ulcers. Its effectiveness against clarithromycin-resistant strains provides hope that it can form the basis for an alternative therapeutic agent against H. pylori.
Revised April 7, 2004
Accepted April 10, 2004
Brief report
In vitro anti-Helicobacter pylori activity of Extractum liquiritiae, glycyrrhizin and its metabolites
2 Raphael-Pharmacy, Westerhorn, Germany
3 Institute of Pharmacy, Department of Pharmaceutical Biology, University of Kiel, Germany
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Abstract
106-107 cfu/mL) at 0, 4, 24, 48, 72 and 96 h.
50 mg/L. Clarithromycin-resistant strains were susceptible at 12.5 and 25 mg/L, and metronidazole-resistant strains at 25-50 and at 200 mg/L. The MIC distribution (mg/L) of aGAMG was
6.25 (29.2%), 50 (4.2%), 100-200 (12.5%) and
400 (54.1%). EL and GL were less active (MICs >400 mg/L). GA exhibited rapid, concentration and strain-dependent bactericidal activity.![]()
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