These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Epithelial modulation of antigen-induced tracheal smooth muscle contractions in actively sensitized guinea-pigs.
    Author: Egilmez Y, Ilhan M.
    Journal: Arch Int Pharmacodyn Ther; 1992; 320():81-92. PubMed ID: 1300944.
    Abstract:
    Coaxial bioassay system (guinea-pig trachea and rat anococcygeus muscle as donor and bioassay organs, respectively) and tracheal open ring preparations from ovalbumin-sensitized guinea-pigs were used to investigate the role of the epithelium in response to the antigen challenge. Ovalbumin induced concentration-dependent relaxations in the phenylephrine precontracted rat anococcygeus muscle suspended in the lumen of sensitized guinea-pig tracheal tube preparations in the presence of either indomethacin or mepacrine. Removal of the epithelium abolished ovalbumin-induced relaxation responses. In tracheal open ring preparations, epithelium removal shifted the ovalbumin concentration-response curve to the left in both the control and mepacrine-treated experiments. Indomethacin significantly potentiated the ovalbumin-induced contractions in epithelium-intact preparations, while in epithelium-denuded ones no significant change was observed. In the presence of indomethacin, the maximum contractile responses were significantly higher in epithelium-intact preparations than in epithelium-denuded ones. These results provide direct evidence for the release of epithelium-derived relaxant factor(s), which is (are) neither a cyclooxygenase nor a lipoxygenase product, in response to the antigen challenge. In addition, the observation of the increased maximum contraction to antigen in epithelium-intact preparations in the presence of indomethacin, suggests the involvement of contractile influences derived from the epithelium in antigen-induced responses of airways.
    [Abstract] [Full Text] [Related] [New Search]