Mucoactive drugs      

Main Article Content

Anna Zasowska-Nowak
Dariusz Nowak

Abstract

The production of mucus is the first-line defense against inhaled harmful agents damaging the airway epithelium. The process in which airway mucus together with microbes, viruses and other particles trapped within is moved out of the respiratory tract, is termed mucociliary clearance. The effective ciliary movement and biophysical properties of mucus, especially its two features; viscosity and elasticity, affect on efficiency of this process. Under normal conditions airway mucus protects the lower respiratory tract against inhaled irritants. On the other hand, excessive production of airway mucus in respiratory diseases, such as chronic obstructive pulmonary disease, asthma or cystic fibrosis, is associated with number of complications. Mucus hypersecretion, related with changes in its biophysical properties, can weaken mucociliary clearance as well as favour accumulation of mucus in upper and lower airways. Mucoactive drugs, stimulating airway clearance, are one of the therapeutic options in these cases. According to the putative mechanism of action, these compounds are categorized to four main groups, as expectorants (induce cough), mucolytics (increase mucus viscosity), mucokinetics (facilitate ciliary movement) and mucoregulators (act on hypersecretion). It is noteworthy, that many of them have other beneficial effects besides influence on mucus and mucociliary clearance. For example, the experimental and clinical studies on erdosteine indicate its antioxidant, anti-inflammatory, antibacterial and mucolytic pharmacological activities. Although over 50 compounds have potentially profitable effect on airway mucus, the mechanism of action of numerous of it is imprecisely characterized or absolutely unknown. The accessible data does not interchangeably confirm benefits from use of mucoactive drugs, that is why the further studies on efficacy of its action should be carrying out.


 

Downloads

Download data is not yet available.

Article Details

How to Cite
Zasowska-Nowak , A., & Nowak , D. (2010). Mucoactive drugs      . Alergoprofil, 6(1), 7-13. Retrieved from https://journalsmededu.pl/index.php/alergoprofil/article/view/167
Section
Article

References

1. Rogers D.F.: Physiology of airway mucus secretion and patophysiology of hypersecretion. Respir. Care 2007, 52: 1134.
2. Rogers D.F.: Mucoactive agents for airway mucus hypersecretory diseases. Respir. Care 2007, 52: 1176.
3. Rogers D.F.: Airway mucus hypersecretion in asthma: an undervalued pathology? Curr. Opin. Pharmacol. 2004, 4: 241.
4. Rogers D.F.: The role of airway secretions in COPD: patophysiology, epidemiology, and pharmacotherapeutic options. COPD 2005, 2: 341.
5. Wiessmann K.J., Niemeyer K.: Clinical results in the treatment of chronic obstructive bronchitis with ambroxol in comparison with bromhexine. Arzneimittelforschung 1978, 28: 918.
6. Melerba M., Ragnoli B.: Ambroxol in the 21st century: pharmacological and clinical update. Expert Opin. Drug Metab. Toxicol. 2008, 4: 1119.
7. Pressler T.: Review of recombinant human deoxyribonuclease (rhDNase) in the management of patients with cystic fibrosis. Biologics 2008, 2: 611.
8. Ruri R.: The use of human deoxyribonuclease (rhDNase) in the management of cystic fibrosis. BioDrugs 2005, 19: 135.
9. Dekhuijzen P.N., van Beurden W.N.: The role of N-acetylcysteine in the management of COPD. Int. J. Chron. Obstruct. Pulmon. Dis. 2006, 1: 99.
10. Sadowska A.M., Verbraecken J., Darquennes K., De Backer W.A.: Role of N-acetylcysteine in the management of COPD. Int. J. Chron. Obstruct. Pulmon. Dis. 2006, 1: 425.
11. Rozpoznawanie i leczenie przewlekłej obturacyjnej choroby płuc. Wytyczne Światowej Inicjatywy Zwalczania Przewlekłej Obturacyjnej Choroby Płuc (GOLD 2006).
12. Kasielski M., Nowak D.: Long-term administration of N-acetylcysteine decreases hydrogen peroxide exhalation in subjects with chronic obstructive pulmonary disease. Respir. Med. 2001, 95: 448.
13. Pela R., Calcagni A.M., Subiaco S., Isidori P., Tubaldi A., Sanguinetti C.M.: N-acetylcysteine reduces the exacerbation rate in the patients with moderate to severe COPD. Respiration 1999, 66: 495.
14. Sutherland E.R., Crapo J.D., Bowler R.P.: N-acetylcysteine and exacerbations of chronic obstructive pulmonary disease. COPD 2006, 3: 195.
15. Decramer M., Rutten-van Mölken M., Dekhuijzen P.N., Troosters T., van Herwaarden C., Pellegrino R., van Schayck C.P., Olivieri D., Del Donno M., De Backer W., Lankhorst I., Ardia A.: Effects of N-acetylcysteine on outcomes in chronic obstructive pulmonary disease (Bronchitis Randomized on NAC Cost-Utility Study, BRONCUS): a randomised placebo-controlled trial. Lancet 2005, 365: 552.
16. Hooper C., Calvert J.: The role for S-carboxymethylcysteine (carbocisteine) in the management of chronic obstructive pulmonary disease. Int. J. Chron. Obstruct. Pulmon. Dis. 2008, 3: 659.
17. Moretti M.: Pharmacology and clinical efficacy of erdosteine in chronic obstructive pulmonary disease. Expert Rev. Resp. Med. 2007, 1: 307.
18. Dal Sasso M., Sala M.T., Gianelle V.: Effects of erdosteine and its metabolites on bacterial adhesiveness. Arzneimittelforschung 1999, 49: 344.
19. Marchioni C.F., Polu J.M., Taytard A., Hanard T., Noseda G., Mancini C.: Evaluation of efficacy and safety of erdosteine in patients affected by chronic bronchitis during an infective exacerbation phase and receiving amoxycillin as basic treatment (ECOBES, European Chronic Obstructive Bronchitis Erdosteine Study). Int. J. Clin. Pharmacol. Ther. 1995, 33: 612.
20. Ricevuti G., Mazzone A., Uccelli E., Gazzani G., Fregnan G.B.: Influence of erdosteine, a mucolytic agent, on amoxycillin penetration into sputum in patients with an infective exacerbation of chronic bronchitis. Thorax 1988, 43: 585.
21. Braga P.C., Dal Sasso M., Zuccotti T.: Assessment of the antioxidant activity of the SH metabolite I of erdosteine on human neutrophil oxidative bursts. Arzneimittelforschung 2000, 50: 739.
22. Braga P.C., Dal Sasso M., Culici M., Verducci P., Lo Verso R., Marabini L.: Effect of metabolite I of erdosteine on the release of human neutrophil elastase. Pharmacology 2006, 77: 150.
23. Braga P.C., Dal Sasso M., Zuccotti T.: Assessment of the antioxidant activity of the SH metabolite I of erdosteine on human neutrophil oxidative bursts. Arzneimittelforschung 2000, 50: 739.
24. Dal Sasso M., Bovio C., Culici M., Fonti E., Braga P.C.: The SH-metabolite I of erdosteine, a mucolytic drug, enhances the inhibitory effect of salbutamol on the respiratory burst of neutrophils. Drugs Exp. Clin. Res. 2002, 28: 147.
25. Moretti M., Bottrighi P., Dallari R. et al.: The effect of long-term treatment with erdosteine on chronic obstructive pulmonary disease: the EQUALIFE Study. Drugs Exp. Clin. Res. 2004, 30: 143.
26. Marchioni C.F., Polu J.M., Taytard A., Hanard T., Noseda G., Mancini C.: Evaluation of efficacy and safety of erdosteine in patients affected by chronic bronchitis during an infective exacerbation phase and receiving amoxycillin as basic treatment (ECOBES, European Chronic Obstructive Bronchitis Erdosteine Study). Intern. J. Clin. Pharmacol. Ther. 1995, 33: 612.
27. Poole P.J., Black P.N.: Mucolytic agents for chronic bronchitis or obstructive pulmonary disease. Cochrane Database of Systematic Reviews 2006, 3: CD001287.
28. Grandjean E.M. et al.: Efficacy of oral long term N-acetylcysteine in chronic bronchopulmonary disease: a metaanalysis of published double-blind, placebo-controlled clinical trials. Respir. Therap. 2000, 22: 209.