Abstract
Reactive oxygen species, including hydrogen peroxide (H2O2), are released from activated leucocytes and resident cells in the joint during inflammation. We hypothesize that H2O2 is an important mediator of inflammatory pain and, thus, the aim of our experiments was to investigate the effect of H2O2 on inflammation of the mouse hindpaw. We performed behavioural studies in CD1 mice to determine the effect of H2O2 on both thermal and mechanical hyperalgesia and oedema formation 20 minutes after intraplantar injection into the mouse hindpaw. The Hargreaves technique was used to test thermal hyperalgesia and a dynamic plantar aesthesiometer was used for mechanical hyperalgesia studies. Oedema was determined by measuring paw mass. Our experiments showed intraplantar injection of H2O2 (2200–8800 nmoles) causes significant thermal and mechanical hyperalgesia of the mouse hindpaw. H2O2 also causes significant oedema formation. Thus, we propose that H2O2 is a potential target for the treatment of inflammatory pain.
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Keeble, J.E., Bodkin, J.V., Russell, F.A. et al. A role for hydrogen peroxide in inflammatory hyperalgesia of the mouse hindpaw. Inflamm. Res. 56 (Suppl 3), S492–S494 (2007). https://doi.org/10.1007/BF03353887
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DOI: https://doi.org/10.1007/BF03353887