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Published on: July 28, 2023
In-vitro activity of lansoprazole against Helicobacter pylori
N Figura1, J E Crabtree, M Dattilo
1Institute of Internal Medicine, University of Siena, Italy. figura@unisi.it
Abstract:
Lansoprazole is a gastric parietal cell proton pump inhibitor that is also active against Helicobacter pylori in vitro. We aimed to investigate further the mechanism of its antimicrobial effect. The antimicrobial activity of lansoprazole and of its sulfenamide, a rearrangement product occurring spontaneously in acid environments, was studied by determining the MICs and MBCs for 11 cytotoxic and eight non-cytotoxic H. pylori strains and by measuring the rapidity of bacterial killing. The MIC90 and MBC90 were 2.5 mg/L and 10 mg/L, respectively, both for lansoprazole and for its sulfenamide. Cytotoxic strains were as susceptible as non-cytotoxic strains. The sulfenamide exhibited faster bactericidal activity. Lansoprazole did not inhibit the toxin-induced vacuolization of HeLa cells by a cytotoxic strain, hence its anti-H. pylori activity does not depend on inhibition of a v-ATPase-mediated, toxin-induced activity. Sulfenamide formation is likely to occur in vivo in the gastric environment, thus enhancing the bactericidal activity of the drug. Lansoprazole is likely to be useful, in association with antibiotics, in the treatment of H. pylori infection regardless of the cytotoxicity of the infecting strain.
Insights
Lansoprazole effectively kills Helicobacter pylori, with its sulfenamide form showing faster action. This proton pump inhibitor is a promising addition to antibiotic treatments for H. pylori infections.
Area of Science:
- Microbiology
- Pharmacology
Background:
- Lansoprazole, a proton pump inhibitor, demonstrates in vitro activity against Helicobacter pylori.
- The precise mechanism of lansoprazole's antimicrobial effect requires further elucidation.
Purpose of the Study:
- To investigate the antimicrobial mechanism of lansoprazole against Helicobacter pylori.
- To compare the activity of lansoprazole and its sulfenamide derivative against H. pylori strains.
Main Methods:
- Determining Minimum Inhibitory Concentrations (MICs) and Minimum Bactericidal Concentrations (MBCs) for lansoprazole and its sulfenamide against 19 H. pylori strains.
- Assessing the rate of bacterial killing and evaluating the effect on toxin-induced vacuolization in HeLa cells.
Main Results:
- Lansoprazole and its sulfenamide exhibited similar MIC90 (2.5 mg/L) and MBC90 (10 mg/L) values against H. pylori.
- Cytotoxic and non-cytotoxic H. pylori strains showed comparable susceptibility.
- The sulfenamide derivative demonstrated more rapid bactericidal activity.
- Lansoprazole did not inhibit toxin-induced vacuolization, indicating its anti-H. pylori activity is independent of v-ATPase inhibition.
Conclusions:
- Sulfenamide formation in acidic gastric environments likely enhances lansoprazole's in vivo bactericidal activity.
- Lansoprazole, potentially in combination with antibiotics, is a viable treatment option for H. pylori infections, irrespective of bacterial cytotoxicity.
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