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Research Article Free access | 10.1172/JCI116644

Modulation of cholinergic neural bronchoconstriction by endogenous nitric oxide and vasoactive intestinal peptide in human airways in vitro.

J K Ward, M G Belvisi, A J Fox, M Miura, S Tadjkarimi, M H Yacoub, and P J Barnes

Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London, United Kingdom.

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Published August 1, 1993 - More info

Published in Volume 92, Issue 2 on August 1, 1993
J Clin Invest. 1993;92(2):736–742. https://doi.org/10.1172/JCI116644.
© 1993 The American Society for Clinical Investigation
Published August 1, 1993 - Version history
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Abstract

Human airway smooth muscle possesses an inhibitory nonadrenergic noncholinergic neural bronchodilator response mediated by nitric oxide (NO). In guinea pig trachea both endogenous NO and vasoactive intestinal peptide (VIP) modulate cholinergic neural contractile responses. To identify whether endogenous NO or VIP can modulate cholinergic contractile responses in human airways in vitro, we studied the effects of specific NO synthase inhibitors and the peptidase alpha-chymotrypsin on contractile responses evoked by electrical field stimulation (EFS) at three airway levels. Endogenous NO, but not VIP, was shown to inhibit cholinergic contractile responses at all airway levels but this inhibition was predominantly in trachea and main bronchus and less marked in segmental and subsegmental bronchi. To elucidate the mechanism of this modulation we then studied the effects of endogenous NO on acetylcholine (ACh) release evoked by EFS from tracheal smooth muscle strips. We confirmed that release was neural in origin, frequency dependent, and that endogenous NO did not affect ACh release. These findings show that endogenous NO, but not VIP, evoked by EFS can inhibit cholinergic neural responses via functional antagonism of ACh at the airway smooth muscle and that the contribution of this modulation is less marked in lower airways.

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