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(Chest. 2003;124:633-638.)
© 2003 American College of Chest Physicians

Nitric Oxide Metabolites Are Not Reduced in Exhaled Breath Condensate of Patients With Primary Ciliary Dyskinesia*

Zsuzsanna Csoma, MD; Andrew Bush, MD; Nicola M. Wilson, MD; Louise Donnelly, PhD; Beatrix Balint, MD; Peter J. Barnes, DM and Sergei A. Kharitonov, MD, PhD

* From the Departments of Thoracic Medicine (Drs. Csoma, Balint, Donnelly, Barnes, and Kharitonov) and Pediatric Respiratory Care (Drs. Bush and Wilson), Imperial College School of Medicine, National Heart and Lung Institute, London, UK.

Correspondence to: Peter J. Barnes, DM, Department of Thoracic Medicine, Imperial College School of Medicine, National Heart and Lung Institute, Dovehouse St, London, SW3 6LY, United Kingdom; e-mail: p.j.barnes{at}ic.ac.uk


   Abstract
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 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Study objectives: To investigate whether nitric oxide (NO) metabolites would be reduced in children affected by primary ciliary dyskinesia (PCD).

Design: Single-center observational study.

Patients: Fifteen children with PCD (seven boys; mean [± SEM] age, 10.3 ± 0.7 years; mean FEV1, 73 ± 2.1% predicted) were recruited along with 14 healthy age-matched subjects (seven boys; mean age, 11.5 ± 0.4 years; mean FEV1, 103 ± 5% predicted).

Interventions: We assessed the levels of nitrite (NO2-), NO2-/NO3- (NO2-/NO3-), and S-nitrosothiol in exhaled breath condensate, exhaled NO, and nasal NO from children with PCD compared to those in healthy children.

Measurements and results: The mean exhaled and nasal NO levels were markedly decreased in children with PCD compared to those without PCD (3.2 ± 0.2 vs 8.5 ± 0.9 parts per billion [ppb], respectively [p < 0.0001]; 59.6 ± 12.2 vs 505.5 ± 66.8 ppb, respectively [p < 0.001]). Despite the lower levels of exhaled NO in children with PCD, no differences were found in the mean levels of NO2- (2.9 ± 0.4 vs 3.5 ± 0.3 µM, respectively), NO2-/NO3- (35.2 ± 5.0 vs 34.3 ± 4.5 µM, respectively), or S-nitrosothiol (1.0 ± 0.2 vs 0.6 ± 0.1 µM, respectively) between children with PCD and healthy subjects.

Conclusion. These findings suggest that NO synthase activity may not be decreased as much as might be expected on the basis of low exhaled and nasal NO levels.

Key Words: breath condensate • exhaled nitric oxide • nitrite • nitrite/nitrate • primary ciliary dyskinesia • S-nitrosothiols


   Introduction
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 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Primary ciliary dyskinesia (PCD), including Kartagener syndrome, is a genetic disease that is characterized by defective motility of cilia, in which the levels of exhaled and nasal nitric oxide (NO) are very low compared to healthy subjects.1 2 3 Such low values of exhaled and nasal NO are not seen in patients with any other condition and are, therefore, of diagnostic value.4 5

The measurement of exhaled NO might be used as a screening procedure to detect PCD among patients with recurrent chest infections or male infertility due to immotile spermatozoa, and the diagnosis of PCD would then be confirmed by the saccharine test, nasal NO level, ciliary beat frequency (CBF), and electron microscopy.6 NO plays an important role in bactericidal activity in the lungs, sodium and chloride transport in the nasal epithelium, and CBF,7 so that a decrease in endogenous NO production might contribute to the characteristic recurrent chest infections in PCD patients. Low levels of exhaled and nasal NO in PCD patients are related to mucociliary dysfunction,1 8 and treatment with NO donor L-arginine increases nasal NO levels and also improves mucociliary transport in PCD patients.1 9 Considering the inflammatory nature of PCD, the markedly decreased exhaled and nasal NO levels are surprising, and the pathophysiologic basis of these observations are still not clear.

NO is a free radical that is rapidly oxidized, reduced, or complexed with other molecules depending on the microenvironment, leading to the formation of nitrite (NO2-), nitrate (NO3-), and powerful oxidant peroxynitrite (ONOO-).10 11 ONOO- formation may be decreased in patients with PCD due to the NO deficit. It may further impair host defense in patients with PCD, as ONOO- may also nitrate inflammatory proteins such as the chemokines and, therefore, reduce oxidative damage.12 In addition, ONOO- interacts directly with glutathione to form the nitrososthiol S-nitrosoglutathione, which may protect against further effects of ONOO-.13

NO metabolites, such as NO2-, NO3-, and S-nitrosothiol, previously have been detected in exhaled breath condensate.14 We speculated that the measurement of NO metabolites in exhaled breath condensate would provide further information about nitrogen-reactive species in the airways of patients with PCD. We hypothesized that, on the basis of the low levels of exhaled and nasal NO, exhaled NO metabolites would be low. The design of this study was to assess the levels of NO2-, NO3, and S-nitrosothiol in the exhaled breath condensate of children with PCD in comparison with healthy subjects.


   Materials and Methods
TOP
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Patients
Patients were recruited from the pediatric PCD Clinic at the Royal Brompton Hospital. PCD was diagnosed by nasal brushing with an estimation of CBF and the determination of ultrastructural defects using electron microscopy. We studied 15 patients with PCD (seven boys; mean [± SEM] age, 10.3 ± 0.7 years; age range, 7 to 14 years) who had a mean FEV1 of 73 ± 2.1% of predicted. Eight patients were receiving therapy with inhaled corticosteroids. The age-matched control group consisted of 14 healthy children (seven boys; mean age, 11.5 ± 0.4 years; mean FEV1, 103 ± 5.0% of predicted) without a history of chronic or recent acute respiratory disease, who were healthy siblings of children who were attending the asthma clinic at Royal Brompton Hospital or were the children of staff members. The characteristics of the subjects are shown in Table 1 . The protocol was approved by the Ethics Committee of the Royal Brompton and Harefield National Health Service Trust, and informed consent was obtained from all parents and children recruited into the study.


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  		Table 1.. Subject Characteristics*

 
Study Design
Subject details were obtained, and then baseline spirometry testing was performed, and exhaled NO and nasal NO levels were measured, followed by the collection of exhaled breath condensate.

Pulmonary Function
FVC percent predicted and FEV1 percent predicted were measured with a dry spirometer (Vitalograph; Buckingham, UK), and the best value of three maneuvers was expressed as a percentage of the predicted value.

Exhaled NO Measurement
NO was measured by chemiluminescence analyzer (model LR2000; Logan Research Ltd; Rochester, UK) according to American Thoracic Society guidelines15 and European Respiratory Society guidelines16 on NO measurements, as described previously.2 17

Exhaled Breath Condensate
Exhaled breath condensate was collected by using a condenser, which allowed the noninvasive collection of nongaseous components of the expiratory air (EcoScreen; Jaeger; Würzburg, Germany), as described previously.14 Subjects breathed through a mouthpiece and a two-way nonrebreathing valve, which also served as a saliva trap. They were asked to breathe at a normal frequency and at tidal volume, wearing a nose clip, for a period of 8 min. The condensate, at least 700 µL, was collected on ice at -20°C and was stored at -70°C immediately.

NO2-, NO2- and NO3-, and S-Nitrosothiol Measurements
The quantification of NO2- was assessed by a fluorometric assay based on the reaction of NO2- with 2,3-diaminonaphthalene to form the fluorescent product 1-(H)-naphthotriazole.23 Briefly, the 100-µL sample (exhaled breath condensate) was mixed with 10 µL 0.05 mg/mL 2,3-diaminonaphthalene reagent in 0.625 M HCl. The reaction was allowed to proceed at room temperature in the dark and was terminated with the addition of 10 µL 1.4 M NaOH. The intensity of the fluorescent signal produced by the product was measured by a fluorometer (Biolite F1; Labtech International Ltd; Uckfield, UK) immediately. The incubation of samples with NO3- reductase allowed the NO3- present in the sample to be measured by this assay after being converted to NO2-.14 S-nitrosothiols were measured following the release of NO2- from S-nitrosothiols by 2 mM Hg2Cl using the above-mentioned procedure.14 To calculate the level of S-nitrosothiols, NO2- levels were subtracted.

Statistical Analysis
Data were expressed as the mean ± SEM. A Mann-Whitney test was used to compare groups. The correlation between the fractional concentration of exhaled NO and NO2-, NO2-/NO3-, and S-nitrosothiol, as well as NO metabolites and lung function (ie, FEV1) was determined by nonparametric Spearman correlation analysis. Significance was defined as a value of p < 0.05.


   Results
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 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Lower and Upper Airway NO
The mean exhaled NO levels were significantly decreased in PCD patients compared to those in healthy subjects (3.2 ± 0.2 vs 8.4 ± 0.9 parts per billion [ppb], respectively; p < 0.0001) [Fig 1 ]. There was no significant difference between the steroid-naive and steroid-treated groups (3.4 ± 0.3 vs 3.0 ± 0.3 ppb, respectively). There was no correlation between exhaled NO and FEV1, NO2-, NO2-/NO3- and S-nitrosothiol levels in exhaled breath condensate. Upper airway NO levels also were found to be markedly reduced in children with PCD compared to healthy control subjects (59.6 ± 12.2 vs 505.5 ± 66.8 ppb, respectively; p < 0.001).



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  		Figure 1.. Top left, A: S-nitrosothiol levels in the exhaled breath condensate of healthy subjects and patients with PCD. Top right, B: NO2- levels in the exhaled breath condensate of healthy subjects and patients with PCD. Bottom left, C: NO2- and NO3- levels in the exhaled breath condensate of healthy subjects and patients with primary PCD. Bottom right, D: NO levels in the exhaled air of healthy subjects and patients with primary PCD.

 
NO2-, NO2-/NO3-, and S-Nitrosothiols in Breath Condensate
There was no significant difference in the levels of NO2- (2.9 ± 0.4 vs 3.5 ± 0.3 µM, respectively), NO2-/NO3- (35.2 ± 5.0 vs 34.3 ± 4.5 µM, respectively), and S-nitrosothiol (1.0 ± 0.2 vs 0.6 ±0.1 µM, respectively) in exhaled breath condensate between patients with PCD and healthy subjects. No differences were found in the levels of NO2-, NO2-/NO3-, and S-nitrosothiol (2.8 ± 0.7 vs 3.1 ±0.5 µM, respectively; 34.1 ± 6.6 vs 36.5 ± 8.1 µM, respectively; and 1.0 ± 0.3 vs 1.0 ± 0.2 µM, respectively) in exhaled breath condensate from steroid-naive and steroid-treated PCD patients and between patients who were or were not receiving long-term antibiotic treatment (3.2 ± 0.7 vs 2.6 ± 0.5 µM, respectively; 34.2 ± 7.9 vs 36.3 ± 6.3 µM, respectively; and 1.3 ± 0.3 vs 0.6 ± 0.2 µM, respectively). There was no correlation among NO2-, NO2-/NO3-, and S-nitrosothiol levels in exhaled breath condensate, and also no correlation was found among exhaled NO levels, FEV1 and NO2-, NO2-/NO3-, and S-nitrosothiol levels.


   Discussion
TOP
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
This study was designed to investigate whether the levels of NO metabolites, such as NO2-, NO2-/NO3-, and S-nitrosothiol, in exhaled breath condensate were reduced in PCD patients, as might be expected from the lower levels of exhaled and nasal NO that have been described previously.1 2 Surprisingly, no differences were found in the levels of exhaled NO2-, NO2-/NO3-, or exhaled S-nitrosothiol between patients with PCD and healthy subjects. There was a trend toward decreased exhaled NO2- levels in patients with PCD compared to healthy subjects. The levels of S-nitrosothiols were not decreased in PCD when compared to healthy subjects. Indeed, there was a tendency toward elevated levels.

The normal levels of NO metabolites cast doubt on the hypothesis that reduced exhaled and nasal NO levels are the results of reduced NO synthase (NOS) activity. Nevertheless, reduced NOS activity cannot be completely excluded. Normal NOS activity is comparable with a decreased level of exhaled NO if increased NO metabolism or reduced NO diffusion into the airway lumen occurs. Elevated levels of NO2- and NO3-,18 19 and nitrotyrosine20 have been found in the exhaled condensate and sputum21 of patients with cystic fibrosis (CF) during clinical stability and during exacerbations. In children with CF and normal lung function, however, the NO2-/NO3- concentrations in BAL fluid are normal and concentrations of S-nitrosothiol are reduced.22 In contrast, elevated levels of NO2- and S-nitrosothiol are found in the exhaled breath condensate of adult patients with more severe CF.23 Therefore, it may be speculated that production/metabolism changes may take place in PCD patients, so that the total NO production may seem to be similar to those of control subjects.

Myeloperoxidase, which is a heme enzyme of neutrophils that uses hydrogen peroxide to oxidize chloride to hypochlorous acid, is capable of catalyzing the nitration of tyrosine, providing an alternative to ONOO- in the formation of 3-nitrotyrosine.24 At sites of neutrophilic inflammation, the presence of myeloperoxidase will lead to protein nitration because the cosubstrate tyrosine will be available to facilitate the reaction.25 Patients with stable CF have significantly higher levels of nitrotyrosine in exhaled breath condensate than do healthy subjects.20 This suggests that the nitration of proteins by myeloperoxidase may be an additional source of nitrotyrosine in patients with CF who have very low NO production. In fact, the level of myeloperoxidase is elevated in the sputum of CF patients and correlates with concentrations of nitrotyrosine,21 implying that the absence of an increase in exhaled NO does not exclude the possibility of NO participating in airway inflammation, including CF.

Free radicals released from neutrophils may increase NO metabolism by the conversion of NO to NO metabolites, such as NO2-, NO3-, and S-nitrosothiol,26 and may lead to chronic, recurrent neutrophil inflammation, as seen in patients with CF and PCD. In fact, a positive correlation between the NO2- levels in exhaled breath condensate and the number of circulating plasma neutrophils in CF patients has been demonstrated.18

Some bacteria have been shown to produce NO from NO2-.27 NO may play an important role in nonspecific host defense against bacterial, viral, and fungal infections. One of the general mechanisms of antimicrobial defenses involves the S-nitrosylation of NO by cysteine proteases. Therefore, reduced endogenous NO production, resulting in low exhaled and nasal NO levels, may contribute to recurrent chest infections in patients with PCD, CF, and Wegener granulomatosis.28

Patients with PCD are frequently or continuously treated with antibiotics, which can influence nasal and lower airway bacterial composition, which may influence NO production and NO metabolite levels in airway fluids. For example, it has been shown that benzoquinoid ansamycins were able to reduce NO2- accumulation, inducible NOS (iNOS) messenger RNA levels, and the cytokine-dependent activation of the iNOS promoter.29 If this is the case, decreased exhaled NO levels would be associated with elevated levels of NO metabolites in airway fluids. However, our results do not support this hypothesis since no differences were found in the levels of exhaled NO metabolites between patients with PCD and healthy subjects. Furthermore, there were no differences either in the levels of exhaled NO or in the levels of NO metabolites in exhaled breath condensate between patients with PCD who were and were not receiving continuous antibiotic treatment.

Airway hygiene depends largely on mucociliary clearance and the movement of viscoelastic mucus along the airway by the beating of the ciliary appendages of airway epithelial cells.30 The failure to keep the airways sterile by mucociliary clearance, resulting in chronic damage to the airway wall and up-regulation of mucus production, may be due to several of the following factors: (1) very low NO levels in PCD patients because of a deficiency of iNOS; (2) microbial toxin-induced dysfunction of the energy pathways required for ciliary beating (ie, secondary ciliary dyskinesia); and (3) abnormalities in the viscosity of mucus, including reduced salt content/osmolality, which results in it being unsuitable in quality for the cilia to move it. Therefore, methods of recognizing the prevalent mechanism behind the mucociliary clearance in PCD patients may be useful in disease management.

The effect of NO may be beneficial or deleterious, and both NOS inhibitors and substrates of NOS could have great therapeutic potential in the treatment of PCD patients. Currently, L-arginine supplementation has been studied in a variety of clinical situations in which the increase of NO production is desired. For example, digested L-arginine31 and inhaled L-arginine1 have been used in healthy subjects and patients with PCD to improve the bactericidal activity of the lungs, ciliary beating, and mucociliary beating.

Selective and more potent NOS inhibitors and NO donors, as well as noninvasive clinical methods with which to assess NO biochemistry will lead to a better understanding of its deleterious and beneficial effects, and to novel treatments for PCD patients.

In conclusion, our study has demonstrated that the levels of NO metabolites, such as NO2-, NO2-/NO3-, and S-nitrosothiol, in exhaled breath condensate are not different from normal in patients with PCD, despite the marked decrease in exhaled NO levels. This may suggest that NOS activity is not decreased to such an extent as we expected on the basis of the detection of exhaled NO.


   Footnotes
 
Abbreviations: CBF = ciliary beat frequency; CF = cystic fibrosis; iNOS = inducible nitric oxide synthase; NO = nitric oxide; NOS = nitric oxide synthase; NO2- = nitrite; NO3- = nitrate; ONOO- = peroxynitrite; PCD = primary ciliary dyskinesia; ppb = parts per billion

This study was supported by the European and Hungarian Respiratory Society, the Hungarian Immunology and Allergology Society (Hungary), and the National Heart and Lung Institute (UK).

Received for publication June 4, 2002. Accepted for publication December 11, 2002.


   References
TOP
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Loukides, S, Kharitonov, SA, Wodehouse, T, et al (1998) Effect of L-arginine on mucociliary function in primary ciliary dyskinesia. Lancet 352,371-372[ISI][Medline]
  2. Karadag, B, James, AJ, Gultekin, E, et al Nasal and lower airway level of nitric oxide in children with primary ciliary dyskinesia. Eur Respir J 1999;13,1402-1405[Abstract]
  3. Narang, I, Ersu, R, Wilson, NM, et al Nitric oxide in chronic airway inflammation in children: diagnostic use and pathophysiological significance. Thorax 2002;57,586-589[Abstract/Free Full Text]
  4. Kharitonov, SA, Barnes, PJ Exhaled markers of pulmonary disease. Am J Respir Crit Care Med 2001;163,1693-1722[Free Full Text]
  5. Kharitonov, SA, Barnes, PJ Biomarkers of some pulmonary diseases in exhaled breath. Biomarkers 2002;7,1-32[CrossRef][ISI][Medline]
  6. Bush, A Primary ciliary dyskinesia. Acta Otorhinolaryngol Belg 2000;54,317-324[Medline]
  7. Jain, B, Rubinstein, I, Robbins, RA, et al Modulation of airway epithelial cell ciliary beat frequency by nitric oxide. Biochem Biophys Res Commun 1993;191,83-88[CrossRef][ISI][Medline]
  8. Tamaoki, J, Taira, M, Nishimura, K, et al Impairment of airway mucociliary transport in patients with sinobronchial syndrome: role of nitric oxide. J Aerosol Med 2000;13,239-244[ISI][Medline]
  9. Kharitonov, SA, Barnes, PJ Clinical aspects of exhaled nitric oxide. Eur Respir J 2000;16,781-792[Abstract]
  10. Gaston, B, Drazen, JM, Loscalzo, J, et al The biology of nitrogen oxides in the airways. Am J Respir Crit Care Med 1994;149,538-551[Abstract]
  11. van der Vliet, A, Eiserich, JP, Shigenaga, MK, et al Reactive nitrogen species and tyrosine nitration in the respiratory tract: epiphenomena or a pathobiologic mechanism of disease? Am J Respir Crit Care Med 1999;160,1-9[Free Full Text]
  12. Folkerts, G, Kloek, J, Muijsers, RB, et al Reactive nitrogen and oxygen species in airway inflammation. Eur J Pharmacol 2001;429,251-262[CrossRef][ISI][Medline]
  13. Arnelle, DR, Stamler, JS NO+, NO, and NO- donation by S-nitrosothiols: implications for regulation of physiological functions by S-nitrosylation and acceleration of disulfide formation. Arch Biochem Biophys 1995;318,279-285[CrossRef][ISI][Medline]
  14. Balint, B, Donnelly, LE, Hanazawa, T, et al Increased nitric oxide metabolites in exhaled breath condensate after exposure to tobacco smoke. Thorax 2001;56,456-461[Abstract/Free Full Text]
  15. American Thoracic Society.. Recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide in adults and children: 1999; this official statement of the American Thoracic Society was adopted by the ATS Board of Directors, July 1999. Am J Respir Crit Care Med 1999;160,2104-2117[Free Full Text]
  16. Kharitonov, SA, Alving, K, Barnes, PJ Exhaled and nasal nitric oxide measurements: recommendations. Eur Respir J 1997;10,1683-1693[CrossRef][ISI][Medline]
  17. Kharitonov, SA, Chung, FK, Evans, DJ, et al The elevated level of exhaled nitric oxide in asthmatic patients is mainly derived from the lower respiratory tract. Am J Respir Crit Care Med 1996;153,1773-1780[Abstract]
  18. Ho, LP, Innes, JA, Greening, AP Nitrite levels in breath condensate of patients with cystic fibrosis is elevated in contrast to exhaled nitric oxide. Thorax 1998;53,680-684[Abstract/Free Full Text]
  19. Linnane, SJ, Keatings, VM, Costello, CM, et al Total sputum nitrate plus nitrite is raised during acute pulmonary infection in cystic fibrosis. Am J Respir Crit Care Med 1998;158,207-212
  20. Balint, B, Kharitonov, SA, Hanazawa, T, et al Increase nitrotyrosine in exhaled breath condensate in cystic fibrosis. Eur Respir J 2001;17,1201-1207[Abstract/Free Full Text]
  21. Jones, KL, Hegab, AH, Hillman, BC, et al Elevation of nitrotyrosine and nitrate concentrations in cystic fibrosis sputum. Pediatr Pulmonol 2000;30,79-85[CrossRef][ISI][Medline]
  22. Grasemann, H, Gaston, B, Fang, K, et al Decreased levels of nitrosothiols in the lower airways of patients with cystic fibrosis and normal pulmonary function. J Pediatr 1999;135,770-772[CrossRef][ISI][Medline]
  23. Corradi, M, Montuschi, P, Donnelly, LE, et al Nitrosothiols and nitrite in exhaled breath condensate of patients with cystic fibrosis. Am J Respir Crit Care Med 1999;159,A682
  24. van Dalen, CJ, Winterbourn, CC, Senthilmohan, R, et al Nitrite as a substrate and inhibitor of myeloperoxidase: implications for nitration and hypochlorous acid production at sites of inflammation. J Biol Chem 2000;275,11638-11644[Abstract/Free Full Text]
  25. van Dalen, CJ, Winterbourn, CC, Senthilmohan, R, et al Nitrite as a substrate and inhibitor of myeloperoxidase: implications for nitration and hypochlorous acid production at sites of inflammation. J Biol Chem 2000;275,11638-11644[Abstract/Free Full Text]
  26. Jones, KL, Bryan, TW, Jinkins, PA, et al Superoxide causes a reduction in nitric oxide gas and an increase in nitrate. Am J Physiol 1998;275,L1120-L1126
  27. Ji, XB, Hollocher, TC Reduction of nitrite to nitric oxide by enteric bacteria. Biochem Biophys Res Commun 1988;157,106-108[CrossRef][ISI][Medline]
  28. Haubitz, M, Busch, T, Gerlach, M, et al Exhaled nitric oxide in patients with Wegener’s granulomatosis. Eur Respir J 1999;14,113-117[Abstract]
  29. Murphy, P, Sharp, A, Shin, J, et al Suppressive effects of ansamycins on inducible nitric oxide synthase expression and the development of experimental autoimmune encephalomyelitis. J Neurosci Res 2002;67,461-470[CrossRef][ISI][Medline]
  30. Cole, P Pathophysiology and treatment of airway mucociliary clearance: a moving tale. Minerva Anestesiol 2001;67,206-209[Medline]
  31. Kharitonov, SA, Lubec, G, Lubec, B, et al L-arginine increases exhaled nitric oxide in normal human subjects. Clin Sci 1995;88,135-139[Medline]



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