Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1993;52(26):2123-30.
doi: 10.1016/0024-3205(93)90727-k.

Beta-adrenoceptors and the epithelial layer in airways

Affiliations
Review

Beta-adrenoceptors and the epithelial layer in airways

K J Morrison et al. Life Sci. 1993.

Abstract

As an inflammatory disorder of the respiratory system, asthma is characterized by bronchial hyper-responsiveness that appears to involve alterations of the bronchial epithelium. The existence of epithelial beta-receptors is of particular importance to respiratory function, and epithelial dysfunction in asthma may impair beta-adrenoceptor function and lead to bronchial hyper-responsiveness. After reviewing the structure and function of the respiratory epithelium and the role of epithelial beta-adrenoceptors, an in vitro model allowing the detailed study of the regulation of airway smooth muscle by epithelial cells is described. Studies with this model have demonstrated that epithelial beta-adrenoceptors participate in modulating the tone of bronchial smooth muscle cells. Activation of these beta-adrenoceptors leads to bronchial myorelaxation, probably mediated by one or more inhibitory substances generated within the epithelium. In addition, beta-adrenoceptor activity may affect smooth muscle tone indirectly by regulating mucociliary clearance and the paracellular exchange of inflammatory mediators. Since some respiratory diseases seem to be associated with beta-adrenoceptor dysfunction, therapy with beta-agonists may be beneficial by acting on beta-adrenoceptors located both on smooth muscle cells and on epithelial cells.

PubMed Disclaimer

MeSH terms

Substances