Mucus 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 av...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
Human and pig airway submucosal glands secrete mucus in response to substance P (SubP), but in pig t...
International audienceBackground: Bacterial colonization in cystic fibrosis (CF) lungs has been dire...
Mucociliary clearance (MCC) is a critical host innate defense mechanism in airways, and it is impair...
In many species submucosal glands are an important source of tracheal mucus, but the extent to which...
Lung disease in people with cystic fibrosis (CF) is initiated by defective host defense that predisp...
Cystic fibrosis (CF) is caused by dysfunction of the CF transmembrane conductance regulator (CFTR), ...
Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging a...
Mucociliary clearance is a critical defense mechanism for the lungs governed by regionally coordinat...
Cystic fibrosis (CF) is both the most common and most lethal genetic disease in the Caucasian popula...
The intrapulmonary airways conduct air to the alveoli and are defended from inhaled pathogens by a h...
Extracellular nucleotides are among the most potent mediators of mucociliary clearance (MCC) in huma...
Airway diseases, including cigarette smoke-induced chronic bronchitis, cystic fibrosis, and primary ...
Rationale: Cystic fibrosis (CF) airways disease produces a mucoobstructive lung phenotype characteri...
Cystic fibrosis (CF), a genetic disease caused by mutations in the CFTR gene, is a life-limiting dis...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
Human and pig airway submucosal glands secrete mucus in response to substance P (SubP), but in pig t...
International audienceBackground: Bacterial colonization in cystic fibrosis (CF) lungs has been dire...
Mucociliary clearance (MCC) is a critical host innate defense mechanism in airways, and it is impair...
In many species submucosal glands are an important source of tracheal mucus, but the extent to which...
Lung disease in people with cystic fibrosis (CF) is initiated by defective host defense that predisp...
Cystic fibrosis (CF) is caused by dysfunction of the CF transmembrane conductance regulator (CFTR), ...
Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging a...
Mucociliary clearance is a critical defense mechanism for the lungs governed by regionally coordinat...
Cystic fibrosis (CF) is both the most common and most lethal genetic disease in the Caucasian popula...
The intrapulmonary airways conduct air to the alveoli and are defended from inhaled pathogens by a h...
Extracellular nucleotides are among the most potent mediators of mucociliary clearance (MCC) in huma...
Airway diseases, including cigarette smoke-induced chronic bronchitis, cystic fibrosis, and primary ...
Rationale: Cystic fibrosis (CF) airways disease produces a mucoobstructive lung phenotype characteri...
Cystic fibrosis (CF), a genetic disease caused by mutations in the CFTR gene, is a life-limiting dis...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
Human and pig airway submucosal glands secrete mucus in response to substance P (SubP), but in pig t...
International audienceBackground: Bacterial colonization in cystic fibrosis (CF) lungs has been dire...