Helicobacter-induced Gastritis in Mice Not Expressing Metallothionein-I and II

ABSTRACT Background.  Helicobacter pylori a primary cause of gastritis and peptic ulcer disease, is associated with increased production of reactive oxygen species within the gastric mucosa. Metallothionein (MT), a low‐molecular‐weight, cysteine‐rich, metal‐binding ligand, has been shown to sequeste...

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Veröffentlicht in:Helicobacter (Cambridge, Mass.) Mass.), 2003-10, Vol.8 (5), p.533-541
Hauptverfasser: Tran, Cuong D., Huynh, Hien, Van Den Berg, Maartje, Van Der Pas, Mechtelt, Campbell, M. A. Fiona, Philcox, Jeffrey C., Coyle, Peter, Rofe, Allau M., Butler, Ross N.
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Sprache:eng
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Zusammenfassung:ABSTRACT Background.  Helicobacter pylori a primary cause of gastritis and peptic ulcer disease, is associated with increased production of reactive oxygen species within the gastric mucosa. Metallothionein (MT), a low‐molecular‐weight, cysteine‐rich, metal‐binding ligand, has been shown to sequester reactive oxygen species and reduce tissue damage. This study investigates the role of MT in H. pylori‐induced gastritis in mice. Materials and Methods.  Control (MT+/+) and MT‐null (MT–/–) mice were inoculated with either 1 × 108H. pylori or H. felis, and were infected for 4, 8 and 16 weeks or 8 weeks, respectively. H. pylori load was determined by culture. Myloperoxidase activity and MT levels were also determined. Results.  The stomachs of H. felis‐infected mice were more severely inflamed than those of H. pylori‐infected mice. H. felis‐induced gastritis was more severe (p = .003) in MT–/– than in MT+/+ mice. MT–/– mice also had higher (60%; p 
ISSN:1083-4389
1523-5378
DOI:10.1046/j.1523-5378.2003.00174.x