Effects of sulphurous water on human neutrophil elastase release.

Authors: Braga PC (1) , Dal Sasso M (1) , Culici M (1) , Spallino A (1) , Marabini L (1) , Bianchi T (2) , Nappi G (3)
(1) Center of Respiratory Pharmacology, Department of Pharmacology, School of Medicine, University of Milan (2) AVIS Comunale, Milan (3) Center of SPA Thermal Medicine, School of Medicine, University of Milan
Source: Ther Adv Respir Dis. 2010 Dec;4(6):333-40.
DOI: 10.1177/1753465810376783 Publication date: 2010 Dec E-Publication date: July 22, 2010 Availability: abstract Copyright: © 2010, SAGE Publications
Language: English Countries: Not specified Location: Not specified Correspondence address: Braga PC : piercarlo.braga@unimi.It


Article abstract


Molecules bearing a sulphide (HS) group, such as glutathione, play a fundamental role in the defensive system of human airways, as shown by the fact that the lining fluid covering the epithelia of the respiratory tract contains very high concentrations of glutathione: the lungs and nose, respectively, contain about 140 and 40 times the concentrations found in plasma. Consequently, various low-weight soluble molecules bearing an HS group (including N-acetylcysteine, mesna and thiopronine, and prodrugs such as stepronine and erdosteine) have been used for therapeutic purposes. HS groups can also be therapeutically administered by means of sulphurous thermal water containing HS groups. The aim of this study was to investigate the direct activity of such water on the release of elastase by activated human neutrophils.


After the neutrophils were incubated with increasing amounts of sulphurous water or the HS/hydrogen sulphide donor sodium hydrosulphide (NaHS), elastase release was initiated by N-formyl-methionyl-leucyl-phenylalanine and measured by means of spectrofluorimetry using methylsuccinylalanylprolylvalyl-methylcoumarin amide as the fluorogenic substrate. To verify the presence of direct action on elastase we determined the diameter of the area of elastinolysis on elastine-agarose gel plates.


The sulphurous water significantly inhibited elastase release at HS concentrations ranging from 4.5 to 18 μg/ml, as assayed using the iodometric method; in the case of NaHS, the inhibition was significant at HS concentrations ranging from 2.2 to 18 μg/ml. The concentration-effect regression lines of both were parallel and neither showed any direct elastolytic activity.


Previous claims concerning the activity of sulphurous water have been based on the patients' subjective sense of wellbeing and on symptomatic (or general) clinical improvements that are not easy to define or quantify exactly. Our findings indicate that, in addition to its known mucolytic and antioxidant activity, sulphurous water also has an anti-elastase activity that may help to control the inflammatory processes of upper and lower airway diseases.

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