Copyright
©The Author(s) 2015.
World J Crit Care Med. Aug 4, 2015; 4(3): 179-191
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.179
Published online Aug 4, 2015. doi: 10.5492/wjccm.v4.i3.179
Figure 2 Effects of hypertonic saline on the airway surface liquid in cystic fibrosis.
A: In healthy airway epithelia, CFTR plays a vital role in regulating hydration of the airway surface liquid (ASL) constructed of the periciliary layer (PCL) and the mucus layer; B: Due to defective CFTR in individuals with CF, Cl- secretion is impaired and Na+ absorption through ENaC is increased resulting in dehydration of the ASL and accumulation of thick mucus causing reduced PCL height; C: Treatment with hypertonic saline assists osmosis of water into the ASL and thus rehydrates the mucus and partially restores the PCL allowing for easier clearance of mucus. CFTR: Cystic fibrosis transmembrane conductance regulator.
- Citation: Reeves EP, McCarthy C, McElvaney OJ, Vijayan MSN, White MM, Dunlea DM, Pohl K, Lacey N, McElvaney NG. Inhaled hypertonic saline for cystic fibrosis: Reviewing the potential evidence for modulation of neutrophil signalling and function. World J Crit Care Med 2015; 4(3): 179-191
- URL: https://www.wjgnet.com/2220-3141/full/v4/i3/179.htm
- DOI: https://dx.doi.org/10.5492/wjccm.v4.i3.179