Tea tree oil reduces the swelling associated with the efferent phase of a contact hypersensitivity response

Date

2002

Authors

Brand, C.
Grimbaldeston, M.
Gamble, J.
Drew, J.
Finlay-Jones, J.
Hart, P.

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Inflammation Research, 2002; 51(5):236-244

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C. Brand, M. A. Grimbaldeston, J. R. Gamble, J. Drew, J. J. Finlay-Jones, P. H. Hart

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Abstract

<h4>Objective</h4>To examine the anti-inflammatory activities of tea tree oil (TTO) in vivo.<h4>Methods</h4>Mice were sensitized to a chemical hapten, trinitrochlorobenzene, on their ventral skin and 7 days later challenged (or re-exposed) on their dorsal skin with the same hapten.<h4>Results</h4>TTO applied 30 min before or up to 7 h after to the same dorsal site as hapten challenge caused a significant reduction in skin swelling after 24 h. TTO reduced oedema but not the influx of inflammatory cells. This finding was supported by the inability of TTO to suppress TNFalpha-induced E-selectin expression by human umbilical vein endothelial cells. TTO did not suppress irritant- or ultraviolet B-induced oedema.<h4>Conclusion</h4>Topical TTO, specifically the TTO components, terpinen-4-ol and alpha-terpineol can regulate the oedema associated with the efferent phase of a contact hypersensitivity response.

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