Impaired cardiac and peripheral hemodynamic responses to inhaled β₂-agonist in cystic fibrosis

Impaired cardiac and peripheral hemodynamic responses to inhaled β₂-agonist in cystic fibrosis

BACKGROUND: Pulmonary system dysfunction is a hallmark of cystic fibrosis (CF) disease. In addition to impaired cystic fibrosis transmembrane conductance regulator protein, dysfunctional β2-adrenergic receptors (β2AR) contribute to low airway function in CF. Recent observations suggest CF may also b...

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Bibliographic Details
Main Authors: Van Iterson, E. H., Karpen, S. R., Baker, S. E., Wheatley, C. M., Morgan, W. J., Snyder, E. M.
Other Authors: School of Kinesiology, University of Minnesota
Language:en
Published: BioMed Central 2015
Online Access:http://hdl.handle.net/10150/610329
http://arizona.openrepository.com/arizona/handle/10150/610329

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