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Antimicrobial Agents and Chemotherapy, May 2001, p. 1522-1527, Vol. 45, No. 5
Department of Bacteriology, Hyogo College of
Medicine, Nishinomiya, Hyogo 663-8501,1 and
Department of Biological Engineering, Kyushu Institute of
Technology, Iizuka, Fukuoka 820-8502,2 Japan
Received 4 December 2000/Returned for modification 8 January
2001/Accepted 19 February 2001
Lansoprazole and its derivative AG-1789 dose-dependently inhibited
cellular respiration by an endogenous substrate and decreased the ATP
level in Helicobacter pylori cells. The inhibitory
action of lansoprazole and AG-1789 against respiration was specific to substrates such as pyruvate and
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.5.1522-1527.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Inhibitory Activities of Lansoprazole against
Respiration in Helicobacter pylori
-ketoglutarate and similar to the
inhibitory action of rotenone, which is an inhibitor for the mitochondrial respiratory chain. Growth inhibition by lansoprazole and
AG-1789 as well as by rotenone was augmented at high oxygen concentrations under atmospheric conditions. Since the 50% inhibitory concentrations of these compounds for the respiration were close to
their MICs for H. pylori growth, the growth inhibition
might be due to respiratory inhibition by these compounds.
*
Corresponding author. Mailing address: Department of
Bacteriology, Hyogo College of Medicine, 1-1 Mukogawa-cho,
Nishinomiya, Hyogo 663-8501, Japan. Phone: 0798 45 6548. Fax:
0798 40 9162. E-mail: kunagata{at}hyo-med.ac.jp.
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