JAC Advance Access originally published online on January 6, 2003
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Journal of Antimicrobial Chemotherapy (2003) 51, 367-371
© 2003 The British Society for Antimicrobial Chemotherapy
Monotherapy with mastic does not eradicate Helicobacter pylori infection from mice
1 Institute of Infections and Immunity, Floor C, West Block, University Hospital, Queens Medical Centre, University of Nottingham; 2 Division of Microbiology and Infectious Diseases, University of Nottingham, Nottingham NG7 2UH, UK
Received 3 September 2002; returned 10 October 2002; revised 15 October 2002; accepted 23 October 2002
Objective: To determine the ability of mastic monotherapy to eradicate Helicobacter pylori infection from mice.
Materials and methods: The susceptibility of H. pylori SS1 to mastic was assessed by broth dilution determination of the MIC and MBC. Mice were inoculated intragastrically with either a suspension of H. pylori SS1 (n = 70) or brainheart infusion broth alone (n = 10). Mice were given antimicrobial chemotherapy 4 weeks after infection and were administered the mouse equivalent of either 2 g of mastic twice daily for 7 days or a triple therapy regimen containing the mouse equivalent of 400 mg of metronidazole, 250 mg of clarithromycin and 20 mg of omeprazole twice daily for 7 days. Mice were killed either immediately or 1 month after the completion of treatment, and their stomachs cultured for H. pylori.
Results: The mastic MIC and MBC of H. pylori SS1 were 7.80 and 31.25 mg/L, respectively. The triple therapy regimen eradicated infection from 19 of 20 SS1-infected mice. Mastic failed to eradicate infection from any of the 18 SS1-infected mice (P < 0.001) and there was no signifi- cant reduction in gastric bacterial load in mice treated with this regimen.
Conclusion: Despite reported beneficial effects in ulcer patients and the good in vitro activity of mastic against H. pylori, this compound is unable to eradicate H. pylori infection from mice.
Keywords: mastic, Helicobacter pylori, mouse model, eradication
* Corresponding author. Tel: +44-115-924-9924, ext. 42457; Fax: +44-115-970-9923; E-mail: Peter.Jenks{at}nottingham.ac.uk
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