Literature DB >> 3769409

The responsiveness of airway smooth muscle in vitro from dogs with airway hyper-responsiveness in vivo.

E H Walters, P M O'Byrne, P D Graf, L M Fabbri, J A Nadel.   

Abstract

To determine whether smooth muscle from airways made hyper-responsive by ozone exposure is hyper-responsive in vitro, tracheal smooth muscle strips taken from five dogs with airway hyper-responsiveness induced by ozone exposure were compared with strips from five control animals. On 1 day, airway responsiveness was assessed with dose-response curves of acetylcholine aerosol versus pulmonary resistance. On a second day, five dogs were exposed to ozone (3.0 p.p.m. for 2 h) and five were exposed to filtered air. Then airway responsiveness to acetylcholine was reassessed. All dogs were then killed, the trachea was rapidly removed and strips of smooth muscle were prepared from the central one-third of the trachea. The responsiveness of each strip to electrical field stimulation (contractions inhibitable by atropine and tetrodotoxin) and exogenous acetylcholine was assessed after 2 and 6 h of incubation and washing. Ozone caused a marked increase in responsiveness in vivo to acetylcholine with a fall in mean provocation concentration from 0.15 g % to 0.026 g % (P less than 0.001) while sham exposure had no effect. The responsiveness of muscle strips to electrical field stimulation in ozone-exposed dogs after 2 h of incubation and washing was increased when compared with 6 h of incubation and washing and with the control dogs (P less than 0.05 for EF50, the frequency of stimulation giving 50% maximum contraction). However, responsiveness to exogenous acetylcholine was similar in all strips from both ozone-exposed and control dogs.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3769409     DOI: 10.1042/cs0710605

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  2 in total

1.  Pretreatment with antibody to eosinophil major basic protein prevents hyperresponsiveness by protecting neuronal M2 muscarinic receptors in antigen-challenged guinea pigs.

Authors:  C M Evans; A D Fryer; D B Jacoby; G J Gleich; R W Costello
Journal:  J Clin Invest       Date:  1997-11-01       Impact factor: 14.808

Review 2.  Pulmonary neuronal M2 muscarinic receptor function in asthma and animal models of hyperreactivity.

Authors:  R W Costello; D B Jacoby; A D Fryer
Journal:  Thorax       Date:  1998-07       Impact factor: 9.139

  2 in total

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