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Nasal mucosa inflammation induced by oxygen administration in humans
Author(s) -
CAPELLIER G.,
ZHANG Z.,
MAHEU M. F.,
POINTET H.,
RACADOT E.,
KANTELIP B.,
REGNARD J.,
BARALE F.
Publication year - 1997
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1111/j.1399-6576.1997.tb04828.x
Subject(s) - medicine , nostril , nasal lavage , mucous membrane of nose , mucociliary clearance , saline , anesthesia , inflammation , oxygen toxicity , nose , pathology , immunology , allergy , lung , surgery
Background: The effect of oxygen toxicity in human airways is still poorly documented. We prospectively evaluated the inflammatory reaction induced by nasal oxygen exposure in an experimental setting. Methods: Healthy subjects without nasal symptoms were exposed to high FIO2 during 5 h. Oxygen was delivered from a tank at a flow of 41/min to one nostril of each subject and both nostrils were studied. Mucociliary clearance was measured as saccharine nasal transit time (SNTT). Nasal lavage was performed with 5 ml normal saline and the fluid recovered was processed for cytology and measurements of cytokines concentrations: TNFα, IL‐6, IL‐8 and soluble ICAM‐1. Under local anaesthesia, biopsies were performed for immunochemistry and electron microscopy. Results: After oxygen exposure mucociliary clearance decreased and SNTT increased from 16 [9–21] to 20.5 [14–32] min (median and extremes; P < 0.1). In the lavage fluid, concentration of IL‐6 was higher in the oxygen‐exposed nostril (40.5 [11–128] pg/ml) than in the non‐exposed one (7 [0–34] pg/ml; P < 0.05). There was also a trend for a higher IL‐8 in the exposed than in the non‐exposed nostril, (respectively 501 [214–587] pg/ml and 214 [122–616] pg/ml, P < 0.08), and for a higher number of polymorphonuclear cells in exposed nostril. In the mucosal biopsies substance P was not found, but ICAM‐1 expression was higher in the mucosa and submucosa of the exposed nostrils where mast cells were also more abundant and showed piecemeal degranulation. Conclusion: In summary, we found clinical, functional and biological evidence of ongoing nasal inflammation following high FIO 2 inhalation for 5 h. Since the histology and behaviour of nasal and bronchi mucosa are very similar, the same inflammatory events are likely to be occurring in the bronchi upon high concentrations of inhaled oxygen.