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The effects of a kinin antagonist on changes in lung function and plasma extravasation into the airways following challenge of sensitized guinea-pigs

Authors

  • R. L. FEATHERSTONE,

    Corresponding author
    1. Immunopharmacology Group, Clinical Pharmacology, Southampton General Hospital, Southampton, UK
      *Dr R. L. Featherstone, Universität Konsianz, Fakultätfür Biologie, Biochem. Pharmakologie. Postfach 5560 M668, D-78434 Konstanz, Germany.
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  • J. E. PARRY,

    1. Immunopharmacology Group, Clinical Pharmacology, Southampton General Hospital, Southampton, UK
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  • M. K. CHURCH

    1. Immunopharmacology Group, Clinical Pharmacology, Southampton General Hospital, Southampton, UK
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*Dr R. L. Featherstone, Universität Konsianz, Fakultätfür Biologie, Biochem. Pharmakologie. Postfach 5560 M668, D-78434 Konstanz, Germany.

Summary

Background It has been suggested that kinins may play a role in allergic pathophysiology of the airways, contributing to bronchoeonstrietion and oedema formation. Raised levels of kinin generating enzymes and kinins are found in the airways during allergic responses.

Objective Using an in vivo animal model of allergen induced increase in airways resistance we investigated the effects of the brady kinin antagonist Hoe 140, in order to assess the possible contribution of kinins to this response.

Methods Guinea-pigs were sensitized and challenged with ovalbumin (OA) or saline via the endotracheal route and the resulting increase in airways resistance was measured by whole body plethysmography. At 240min after challenge, bronchoalveolar lavage fluid (BALF) was taken and albumin content and kallikrein-like activity defennined by rocket immunoelectrophoresis and use of artificial substrates respec tively. Pretreatment of animals with the bradykinin antagonist Hoe 140 at 6.7, 20 or 66.7nmol/kg or aprotinin (46 000 kallikrein inhibitor units/kg) was by i.p. injection 10 min before challenge.

Results Pre-treatment with Hoe 140 dose dependently attenuated the increase in airways resistance following allergen challenge. Kallikrein-like activity and albumin in BALF were unaltered. Aprotinin reduced the kallikrein-like activity in BALE but did not alter airways resistance.

Conclusion Kinins may contribute to a significant part of allergen-induced airways resistance increase in this model but not via an effect on plasma extravasation.

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