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In Vitro and in Vivo Antibacterial Activities of TAK-083, an Agent for Treatment of Helicobacter Pylori Infection

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Specialty Pharmacology
Date 2001 Aug 15
PMID 11502514
Citations 22
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Abstract

The antibacterial activity of TAK-083 was tested against 54 clinical isolates of Helicobacter pylori and was compared with those of amoxicillin, clarithromycin, and metronidazole. The growth-inhibitory activity of TAK-083 was more potent than that of amoxicillin, clarithromycin, or metronidazole (the MICs at which 90% of the strains are inhibited were 0.031, 0.125, 64, and 8 microg/ml, respectively). The antibacterial activity of TAK-083 was highly selective against H. pylori; there was a >30-fold difference between the concentration of TAK-083 required to inhibit the growth of H. pylori and that required to inhibit the growth of common aerobic and anaerobic bacteria. Exposure of H. pylori strains to TAK-083 at the MIC or at a greater concentration resulted in an extensive loss of viability. When four H. pylori strains were successively subcultured in the medium containing subinhibitory concentrations of TAK-083, no significant change in the MICs of this compound was observed. TAK-083 strongly inhibited the formation of tryptophanyl-tRNA in H. pylori while exhibiting little effect on the same system in eukaryotes. TAK-083 was efficacious in the treatment of gastric infection caused by H. pylori in Mongolian gerbils. The results presented here indicate that TAK-083 is a promising candidate for the treatment of H. pylori infection.

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References
1.
Nomura A, STEMMERMANN G, Chyou P, Perez-Perez G, Blaser M . Helicobacter pylori infection and the risk for duodenal and gastric ulceration. Ann Intern Med. 1994; 120(12):977-81. DOI: 10.7326/0003-4819-120-12-199406150-00001. View

2.
MARSH W, GARRETSON A, WESEL E . PA 155 A, B, and X antibiotics produced by a strain of Streptomyces albus. Antibiot Chemother (Northfield). 1960; 10:316-20. View

3.
Marshall B, Goodwin C, Warren J, Murray R, Blincow E, Blackbourn S . Prospective double-blind trial of duodenal ulcer relapse after eradication of Campylobacter pylori. Lancet. 1988; 2(8626-8627):1437-42. DOI: 10.1016/s0140-6736(88)90929-4. View

4.
Labenz J, Gyenes E, Ruhl G, Borsch G . Amoxicillin plus omeprazole versus triple therapy for eradication of Helicobacter pylori in duodenal ulcer disease: a prospective, randomized, and controlled study. Gut. 1993; 34(9):1167-70. PMC: 1375447. DOI: 10.1136/gut.34.9.1167. View

5.
Sipponen P, Hyvarinen H . Role of Helicobacter pylori in the pathogenesis of gastritis, peptic ulcer and gastric cancer. Scand J Gastroenterol Suppl. 1993; 196:3-6. DOI: 10.3109/00365529309098333. View