The effect of nitric oxide on the permeability of nasal epithelial cells from healthy and asthmatic donors

• Published in: Medical science monitor Vol. 9; no. 7; p. BR276
• Main Authors: Baker, Graham, Chetwin, Karen, Hayward, Kathryn, Bakirtzi, Kyriaki, Willman, Melissa
• Format: Journal Article
• Language: English
• Published: United States 01.07.2003
• Subjects: Adult; Amiloride - metabolism; Animals; Asthma - metabolism; Barium Compounds - metabolism; Calcium Channel Blockers - metabolism; Chlorides - metabolism; Diuretics - metabolism; Electrophysiology; Enzyme Inhibitors - metabolism; Epithelial Cells - cytology; Epithelial Cells - metabolism; Female; Humans; Male; Membrane Potentials; Middle Aged; Nasal Mucosa - cytology; Nitric Oxide - metabolism; Nitric Oxide Donors - metabolism; Nitroprusside - metabolism; ortho-Aminobenzoates - metabolism; Permeability
• ISSN: 1234-1010

To see if the higher levels of nitric oxide expired by asthmatics compared to healthy subjects might be of significance to airway function, the effect of nitric oxide and its second messenger, guanosine 3', 5'- cyclic monophosphate (cGMP), on the permeability of human nasal epithelial cells was studied. Cells from healthy and asthmatic donors, collected by swab biopsy, were plated on agar gel before being impaled with a microelectrode to measure their intracellular potential and membrane resistance. Exposure of cells to 300 mM sodium nitroprusside, a nitric oxide donor, caused a profound fall in both parameters in cells from non-asthmatics but no change in cells from asthmatic subjects. A similar response was seen when cells were exposed to 0.9 mM of the permeable form of cGMP, 8-Br-cGMP. Selective inhibition of ion transport pathways in healthy cells indicated that nitric oxide produced changes in permeability consistent with secretion of anions by the cells. Since anion secretion is associated with fluid secretion in the intact epithelium, we suggest that nitric oxide mediates a protective mechanism to remove foreign material from the airway surface. The defective response to nitric oxide seen in asthmatic cells may contribute to the disease by compromising the removal of allergens from the airway.