Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium

<p>Abstract</p> <p>Introduction</p> <p>The removal of highly viscous mucus from the airways is an important task in the treatment of chronic lung disease like in cystic fibrosis. The inhalation of recombinant human DNase-I (rhDNase-I) is used to facilitate the removal o...

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Main Authors: Rosenecker J, Naundorf S, Rudolph C
Format: Article
Language:English
Published: BMC 2009-07-01
Series:European Journal of Medical Research
Online Access:http://www.eurjmedres.com/content/14/7/304
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spelling doaj-43ff4e43d1b9412f9313d76ee49dbdf72020-11-25T00:26:42ZengBMCEuropean Journal of Medical Research2047-783X2009-07-0114730410.1186/2047-783X-14-7-304Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesiumRosenecker JNaundorf SRudolph C<p>Abstract</p> <p>Introduction</p> <p>The removal of highly viscous mucus from the airways is an important task in the treatment of chronic lung disease like in cystic fibrosis. The inhalation of recombinant human DNase-I (rhDNase-I) is used to facilitate the removal of tenacious airway secretions in different lung diseases and especially in CF. Little is known about endogenous DNase activity in the airway surface liquid. Therefore, we analysed bronchoalveolar lavage fluid (BAL) and exhaled breath condensate (EBC) for the presence of endogenous DNase activity.</p> <p>Methods</p> <p>The degradation of plasmid DNA by BAL from patients who had diagnostic bronchoscopy and bronchoalveolar lavage was analyzed. In a group of CF patients and healthy control volunteers the exhaled breath condensate was obtained and also analyzed for the ability to degrade plasmid DNA. In addition, the ability of magnesium to activate endogenous DNase activity in BAL and exhaled breath condensate was investigated.</p> <p>Results</p> <p>The analyzed BAL samples degraded plasmid DNA only after preincubation with magnesium. When analyzing the exhaled breath condensate the samples obtained from the healthy volunteers showed no DNase activity even after preincubation with magnesium, whereas in one of the two samples obtained from CF patients we found a DNase activity after preincubation with magnesium.</p> <p>Conclusion</p> <p>Increasing the magnesium concentration in the airway surface liquid by aerosolisation of magnesium solutions or oral magnesium supplements could improve the removal of highly viscous mucus in chronic lung disease by activating endogenous DNase activity.</p> http://www.eurjmedres.com/content/14/7/304
collection DOAJ
language English
format Article
sources DOAJ
author Rosenecker J
Naundorf S
Rudolph C
spellingShingle Rosenecker J
Naundorf S
Rudolph C
Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
European Journal of Medical Research
author_facet Rosenecker J
Naundorf S
Rudolph C
author_sort Rosenecker J
title Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
title_short Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
title_full Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
title_fullStr Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
title_full_unstemmed Airway surface liquid contains endogenous DNase activity which can be activated by exogenous magnesium
title_sort airway surface liquid contains endogenous dnase activity which can be activated by exogenous magnesium
publisher BMC
series European Journal of Medical Research
issn 2047-783X
publishDate 2009-07-01
description <p>Abstract</p> <p>Introduction</p> <p>The removal of highly viscous mucus from the airways is an important task in the treatment of chronic lung disease like in cystic fibrosis. The inhalation of recombinant human DNase-I (rhDNase-I) is used to facilitate the removal of tenacious airway secretions in different lung diseases and especially in CF. Little is known about endogenous DNase activity in the airway surface liquid. Therefore, we analysed bronchoalveolar lavage fluid (BAL) and exhaled breath condensate (EBC) for the presence of endogenous DNase activity.</p> <p>Methods</p> <p>The degradation of plasmid DNA by BAL from patients who had diagnostic bronchoscopy and bronchoalveolar lavage was analyzed. In a group of CF patients and healthy control volunteers the exhaled breath condensate was obtained and also analyzed for the ability to degrade plasmid DNA. In addition, the ability of magnesium to activate endogenous DNase activity in BAL and exhaled breath condensate was investigated.</p> <p>Results</p> <p>The analyzed BAL samples degraded plasmid DNA only after preincubation with magnesium. When analyzing the exhaled breath condensate the samples obtained from the healthy volunteers showed no DNase activity even after preincubation with magnesium, whereas in one of the two samples obtained from CF patients we found a DNase activity after preincubation with magnesium.</p> <p>Conclusion</p> <p>Increasing the magnesium concentration in the airway surface liquid by aerosolisation of magnesium solutions or oral magnesium supplements could improve the removal of highly viscous mucus in chronic lung disease by activating endogenous DNase activity.</p>
url http://www.eurjmedres.com/content/14/7/304
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AT naundorfs airwaysurfaceliquidcontainsendogenousdnaseactivitywhichcanbeactivatedbyexogenousmagnesium
AT rudolphc airwaysurfaceliquidcontainsendogenousdnaseactivitywhichcanbeactivatedbyexogenousmagnesium
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