cystic fibrosis airway
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2021 ◽  
Vol 20 ◽  
pp. S267-S268
Author(s):  
M. Easter ◽  
M. Hirsch ◽  
E. Harris ◽  
E. Helton ◽  
G. Bollar ◽  
...  

2021 ◽  
Vol 20 ◽  
pp. S242-S243
Author(s):  
J. O’Connor ◽  
M. Kruk ◽  
A. Mickelson ◽  
B. Wagner ◽  
J. Harris ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Nam Soo Joo ◽  
Hyung-Ju Cho ◽  
Meagan Shinbashi ◽  
Jae Young Choi ◽  
Carlos E. Milla ◽  
...  

AbstractMucus clearance, a primary innate defense mechanism of airways, is defective in patients with cystic fibrosis (CF) and CF animals. In previous work, the combination of a low dose of the cholinergic agonist, carbachol with forskolin or a β adrenergic agonist, isoproterenol synergistically increased mucociliary clearance velocity (MCCV) in ferret tracheas. Importantly, the present study shows that synergistic MCCV can also be produced in CF ferrets, with increases ~ 55% of WT. Synergistic MCCV was also produced in pigs. The combined agonists increased MCCV by increasing surface fluid via multiple mechanisms: increased fluid secretion from submucosal glands, increased anion secretion across surface epithelia and decreased Na+ absorption. To avoid bronchoconstriction, the cAMP agonist was applied 30 min before carbachol. This approach to increasing mucus clearance warrants testing for safety and efficacy in humans as a potential therapeutic for muco-obstructive diseases.


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