We examined epithelial modulation of tracheal smooth muscle (TSM) responsiveness in vitro from guinea pigs receiving active immune sensitization in vivo. Initially, guinea pigs were either ovalbumin sensitized (by aerosol) or sham sensitized with normal saline; TSM responsiveness was assessed isometrically as active tension (AT) after equilibration by electrical field stimulation in vitro. For epithelium-intact (Epi+) tissues, sensitization caused an increase in baseline active spontaneous tone (1.89 +/- 0.20 g AT) vs, sham-sensitized tissues (1.18 +/- 0.20 g AT; P = 0.02). Spontaneous tone in sensitized TSM in which the epithelium was removed (Epi-) (1.01 +/- 0.14 g AT) was substantially less than from Epi+ tissues (P = 0.01) and did not differ from sham-sensitized epithelium-denuded tissues (0.82 +/- 0.24 gAT; P > 0.05). Indomethacin caused a reduction in spontaneous tone to comparable magnitude for all treatment paradigms. Immune sensitization caused physiological reduction in the ability to relax in response to isoproterenol; the concentration of isoproterenol eliciting 50% relaxation of spontaneous tone-was 7.10 +/- 0.13 (-log M) for TSM from sensitized guinea pigs compared with 8.20 +/- 0.27 (-log M) for sham-sensitized tissues (P = 0.006). However, after precontraction with exogenous acetylcholine, relaxation caused by isoproterenol was not affected by either indomethacin or epithelial removal. Muscarinic responsiveness to acetylcholine was augmented by immune sensitization; however, the increase in response to acetylcholine was attenuated by epithelium removal or cyclooxygenase blockade. Our data demonstrate substantial differences in the contractile and relaxant properties of spontaneous tone in vitro that are 1) epithelium dependent and 2) not replicated by contraction with exogenous agonist in the presence of indomethacin. Our data suggest that this augmentation of contraction and reduced ability of beta-adrenergic relaxation of spontaneous tone result from secretion of an epithelial-derived contractile factor that is likely a cyclooxygenase derivative.
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MCMASTER UNIV,FAC HLTH SCI,DEPT NEUROSCI,1200 MAIN ST W,HAMILTON L8N 3Z5,ONTARIO,CANADAMCMASTER UNIV,FAC HLTH SCI,DEPT NEUROSCI,1200 MAIN ST W,HAMILTON L8N 3Z5,ONTARIO,CANADA
MANSOUR, S
DANIEL, EE
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MCMASTER UNIV,FAC HLTH SCI,DEPT NEUROSCI,1200 MAIN ST W,HAMILTON L8N 3Z5,ONTARIO,CANADAMCMASTER UNIV,FAC HLTH SCI,DEPT NEUROSCI,1200 MAIN ST W,HAMILTON L8N 3Z5,ONTARIO,CANADA