Origin of nitrite and nitrate in nasal and exhaled breath condensate and relation to nitric oxide formation

• Published in: Thorax Vol. 60; no. 3; pp. 219 - 225
• Main Authors: Marteus, H, Törnberg, D C, Weitzberg, E, Schedin, U, Alving, K
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Thoracic Society 01.03.2005; BMJ; BMJ Publishing Group LTD; BMJ Group
• Subjects: Adult; Aged; Anti-Infective Agents, Local - pharmacology; Asthma; Biological and medical sciences; Breath Tests; Chlorhexidine - pharmacology; Cystic fibrosis; deionised water; dH2O; EBC; exhaled breath condensate; Exhaled Markers; exhaled nitric oxide; Female; FENO; fraction of expired nitric oxide; Humans; Inflammation; Male; Medical sciences; Medicin och hälsovetenskap; Middle Aged; Mouthwashes - pharmacology; nitrate; Nitrates; Nitrates - administration & dosage; Nitrates - analysis; Nitrates - metabolism; Nitric oxide; Nitric Oxide - metabolism; nitrite; Nitrites - analysis; Nitrites - metabolism; Nose; Nose - chemistry; Ostomy; PCD; Plasma; Pneumology; Poliomyelitis; primary ciliary dyskinesia; Saliva - chemistry; Streptococcus infections; Tracheostomy; Tracheotomy; United States > US; Sweden; Germany; Origin; Expired air; Respiratory disease; Nitric oxide; Nose; Nitrites; Cardiovascular disease; Nitrates; Respiration; Formation
• ISSN: 0040-6376; 1468-3296
• DOI: 10.1136/thx.2004.030635

Background: Raised concentrations of nitrate and nitrite have been found in exhaled breath condensate (EBC) in airway disease, and it has been postulated that this reflects increased nitric oxide (NO) metabolism. However, the chemical and anatomical origin of nitrate and nitrite in the airways has not yet been sufficiently studied. Methods: The fraction of exhaled NO at an exhalation flow rate of 50 ml/s (FENO) and nitrite and nitrate in EBC, nasal condensate, and saliva were measured in 17 tracheostomised and 15 non-tracheostomised subjects, all of whom were non-smokers without respiratory disease. Tracheal and oral samples were taken from the tracheostomised subjects and nasal (during velum closure) and oral samples from the non-tracheostomised subjects. Measurements were performed before and after sodium nitrate ingestion (10 mg/kg) and use of antibacterial mouthwash (chlorhexidine 0.2%). Results: In tracheostomised subjects oral FENO increased by 90% (p<0.01) while tracheal FENO was not affected 60 minutes after nitrate ingestion. Oral EBC nitrite levels were increased 23-fold at 60 minutes (p<0.001) whereas the nitrite levels in tracheal EBC showed only a minor increase (fourfold, p<0.05). Nitrate was increased the same amount in oral and tracheal EBC at 60 minutes (2.5-fold, p<0.05). In non-tracheostomised subjects oral FENO and EBC nitrite increased after nitrate ingestion and after chlorhexidine mouthwash they approached baseline levels again (p<0.001). Nasal NO, nitrate, and nitrite were not affected by nitrate intake or mouthwash. At baseline, mouthwash with deionised water did not affect nitrite in oral EBC or saliva, whereas significant reductions were seen after antibacterial mouthwash (p<0.05 and p<0.001, respectively). Conclusions: Besides the salivary glands, plasma nitrate is taken up by the lower airways but not the nasal airways. Nitrate levels in EBC are thus influenced by dietary intake. Nitrate is reduced to nitrite by bacterial activity which takes place primarily in the oropharyngeal tract of healthy subjects. Only oropharyngeal nitrite seems to contribute to exhaled NO in non-inflamed airways, and there is also a substantial contribution of nitrite from the oropharyngeal tract during standard collection of EBC.