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Airway mucus membrane: effects of beta-adrenergic and anticholinergic stimulation.

Abstract
Mucus hypersecretion and non-continuous clearance of tracheobronchial mucus contribute to airflow obstruction in several pulmonary disease entities. Bronchospasm, which is frequently associated with bronchial asthma, can present simultaneously with mucus transport abnormalities. Therapy designed to dilate airways may produce secondary effects, which are deleterious to effective transport of lung mucus. Sympathomimetic agents, such as beta-adrenergic agonists, reduce the tone of bronchial smooth muscle and enhance the flow of mucus within lung airways. Parasympatholytic agents also improve airflow in the lungs, but their effects at the mucus membrane of the airways may not be beneficial. Atropine, an anticholinergic agent, apparently has dose-dependent effects on human mucociliary function and, administered orally, can reduce large airway mucus transport. However, newer anticholinergic agents, such as ipratropium bromide, are effective bronchodilators and do not exhibit unfavorable effects on lung mucus transport in either subjects with normal mucus secretion or those with hypersecretory disease entities, such as bronchitis. In mildly symptomatic asthmatic patients, aerosolized ipratropium decreased airway obstruction without consistent positive or negative influence on lung mucociliary function.
AuthorsW M Foster, E H Bergofsky
JournalThe American journal of medicine (Am J Med) Vol. 81 Issue 5A Pg. 28-35 (Nov 14 1986) ISSN: 0002-9343 [Print] United States
PMID2878612 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S., Review)
Chemical References
  • Adrenergic beta-Agonists
  • Aerosols
  • Bronchodilator Agents
  • Parasympatholytics
Topics
  • Adrenergic beta-Agonists (pharmacology)
  • Aerosols
  • Asthma (drug therapy, metabolism)
  • Biological Transport (drug effects)
  • Bronchodilator Agents (pharmacology)
  • Epithelium (drug effects, metabolism)
  • Humans
  • Lung (drug effects, metabolism)
  • Mucous Membrane (drug effects, metabolism)
  • Mucus (drug effects, metabolism)
  • Parasympatholytics (pharmacology)
  • Smoking
  • Stimulation, Chemical

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