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Effect of the Carbonic Anhydrase Inhibitor, Acetazolamide, on Helicobacter pylori Infection in vivo: A Pilot Study
Author(s) -
Shahidzadeh Rassa,
Opekun Antone,
Shiotani Akiko,
Graham David Y.
Publication year - 2005
Publication title -
helicobacter
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.206
H-Index - 79
eISSN - 1523-5378
pISSN - 1083-4389
DOI - 10.1111/j.1523-5378.2005.00306.x
Subject(s) - acetazolamide , carbonic anhydrase , helicobacter pylori , urea breath test , in vivo , carbonic anhydrase inhibitor , urea , stomach , medicine , gastroenterology , peptic , gastric acid , pharmacology , enzyme , chemistry , biochemistry , biology , helicobacter pylori infection , peptic ulcer , microbiology and biotechnology
Background. Carbonic anhydrase inhibitors have been successfully used to treat peptic ulcers. Although carbonic anhydrase restriction does not inhibit Helicobacter pylori in vitro, recent studies suggest that carbonic anhydrase inhibition reduces the ability of H. pylori to survive in an acid environment as present in the stomach. Methods. In a pilot study, we examined the effect of acetazolamide 500 mg as twice a day for 4 days in volunteers with active H. pylori infection. Effectiveness was judged by changes in the results of the urea breath test. Results. Eight H. pylori infected volunteers completed the test. No urea breath test reverted to negative and there was a trend for the urea breath test value to increase [e.g. delta over baseline (DOB) mean ± SE increased from 50.9 ± 13 at baseline to 64.9 ± 13 at day 5] during treatment with acetazolamide. Conclusion. The potential effect of carbonic anhydrase inhibitors on acid secretion may prevent effect on H. pylori in vivo and/or the sites of infection at the surface of the stomach may have a pH higher for any postulated acid‐dependent effect to have an effect clinically.