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  1. Book: Human airway inflammation

    Rogers, Duncan F.

    sampling techniques and analytical protocols

    (Methods in molecular medicine ; 56)

    2001  

    Author's details ed. by Duncan F. Rogers
    Series title Methods in molecular medicine ; 56
    Collection
    Keywords Asthma / physiopathology ; Gene Expression Regulation ; Inflammation / diagnosis ; Lung Diseases, Obstructive / pathophysiology
    Language English
    Size XV, 440 S. : Ill., graph. Darst.
    Publisher Humana Press
    Publishing place Totowa, NJ
    Publishing country United States
    Document type Book
    HBZ-ID HT013125021
    ISBN 0-89603-923-4 ; 978-0-89603-923-0
    Database Catalogue ZB MED Medicine, Health

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  2. Book: Airway mucus

    Rogers, Duncan F.

    basic mechanisms and clinical perspectives

    (Respiratory pharmacology and pharmacotherapy)

    1997  

    Author's details ed. by D. F. Rogers
    Series title Respiratory pharmacology and pharmacotherapy
    Keywords Bronchial Diseases / physiopathology ; Mucus / physiology ; Atemwege ; Schleim ; Sekretion ; Atemwegskrankheit ; Pathophysiologie
    Subject Pathologische Physiologie ; Physiologische Pathologie ; Physiopathologie ; Secretion ; Mucus ; Mukus ; Atemwegekrankheit ; Atemwege ; Atemwegserkrankung ; Luftwege ; Respirationstrakt ; Atmungssystem ; Atemsystem ; Apparatus respiratorius
    Language English
    Size X, 388 S. : Ill., graph. Darst.
    Publisher Birkhäuser
    Publishing place Basel u.a.
    Publishing country Switzerland
    Document type Book
    Note Literaturangaben
    HBZ-ID HT008357583
    ISBN 3-7643-5691-X ; 0-8176-5691-X ; 978-3-7643-5691-0 ; 978-0-8176-5691-1
    Database Catalogue ZB MED Medicine, Health

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  3. Article ; Online: Therapeutic options for hydrating airway mucus in cystic fibrosis.

    Tildy, Bernadett E / Rogers, Duncan F

    Pharmacology

    2015  Volume 95, Issue 3-4, Page(s) 117–132

    Abstract: Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the ... ...

    Abstract Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the airway surface liquid due to associated reduced water efflux. PCL layer dehydration reduces mucociliary clearance (MCC), leading to airway obstruction (reduced airflow and inflammation due to pathogen invasion) with mucus plug formation.
    Summary: Rehydrating mucus increases MCC. Mucus hydration can be achieved by direct hydration (administering osmotic agents to set up an osmotic gradient), using CFTR modulators to correct dysfunctional CFTR, or it can be achieved pharmacologically (targeting other ion channels on airway epithelial cells). Key Messages: The molecular mechanisms of several therapies are discussed in the context of pre-clinical and clinical trial studies. Currently, only the osmotic agent 7% hypertonic saline and the CFTR 'potentiator' VX-770 (ivacaftor) are used clinically to hydrate mucus. Emerging therapies include the osmotic agent mannitol (Bronchitol), the intracellular Ca(2+)-raising agent Moli1901/lancovutide, the CFTR potentiator sildenafil [phosphodiesterase type 5 (PDE5) inhibitor] and the CFTR 'corrector' VX-809 (lumacaftor). Other CFTR correctors (e.g. 'chemical chaperones') are also showing pre-clinical promise.
    MeSH term(s) Animals ; Cystic Fibrosis/drug therapy ; Cystic Fibrosis/genetics ; Cystic Fibrosis/metabolism ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Cystic Fibrosis Transmembrane Conductance Regulator/metabolism ; Humans ; Mannitol/therapeutic use ; Mucus/metabolism ; Respiratory System ; Saline Solution, Hypertonic/therapeutic use
    Chemical Substances Saline Solution, Hypertonic ; Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6) ; Mannitol (3OWL53L36A)
    Language English
    Publishing date 2015
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 206671-3
    ISSN 1423-0313 ; 0031-7012
    ISSN (online) 1423-0313
    ISSN 0031-7012
    DOI 10.1159/000377638
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Physiology of airway mucus secretion and pathophysiology of hypersecretion.

    Rogers, Duncan F

    Respiratory care

    2007  Volume 52, Issue 9, Page(s) 1134–46; discussion 1146–9

    Abstract: Mucus secretion is the first-line defense against the barrage of irritants that inhalation of approximately 500 L of air an hour brings into the lungs. The inhaled soot, dust, microbes, and gases can all damage the airway epithelium. Consequently, mucus ... ...

    Abstract Mucus secretion is the first-line defense against the barrage of irritants that inhalation of approximately 500 L of air an hour brings into the lungs. The inhaled soot, dust, microbes, and gases can all damage the airway epithelium. Consequently, mucus secretion is extremely rapid, occurring in tens of milliseconds. In addition, mucus is held in cytoplasmic granules in a highly condensed state in which high concentrations of Ca(2+) nullify the repulsive forces of the highly polyanionic mucin molecules. Upon initiation of secretion and dilution of the Ca(2+), the repulsion forces of the mucin molecules cause many-hundred-fold swelling of the secreted mucus, to cover and protect the epithelium. Secretion is a highly regulated process, with coordination by several molecules, including soluble N-ethyl-maleimide-sensitive factor attachment protein receptor (SNARE) proteins, myristoylated alanine-rich C kinase substrate (MARCKS), and Munc proteins, to dock the mucin granules to the secretory cell membrane prior to exocytosis. Because mucus secretion appears to be such a fundamental airway homeostatic process, virtually all regulatory and inflammatory mediators and interventions that have been investigated increase secretion acutely. When given longer-term, many of these same mediators also increase mucin gene expression and mucin synthesis, and induce goblet cell hyperplasia. These responses induce (in contrast to the protective effects of acute secretion) long-term, chronic hypersecretion of airway mucus, which contributes to respiratory disease. In this case the homeostatic, protective function of airway mucus secretion is lost, and, instead, mucus hypersecretion contributes to pathophysiology of a number of severe respiratory conditions, including asthma, chronic obstructive pulmonary disease, and cystic fibrosis.
    MeSH term(s) Anti-Inflammatory Agents/pharmacology ; Asthma/physiopathology ; Bronchi/drug effects ; Bronchi/physiopathology ; Bronchi/secretion ; Cystic Fibrosis/physiopathology ; Humans ; Inhalation Exposure/adverse effects ; Intracellular Signaling Peptides and Proteins/drug effects ; Intracellular Signaling Peptides and Proteins/physiology ; Membrane Proteins/drug effects ; Membrane Proteins/physiology ; Mucus/drug effects ; Mucus/secretion ; Myristoylated Alanine-Rich C Kinase Substrate ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Respiratory Mucosa/drug effects ; Respiratory Mucosa/physiopathology ; Respiratory Mucosa/secretion ; Respiratory System Agents/pharmacology ; SNARE Proteins/drug effects ; SNARE Proteins/physiology
    Chemical Substances Anti-Inflammatory Agents ; Intracellular Signaling Peptides and Proteins ; MARCKS protein, human ; Membrane Proteins ; Respiratory System Agents ; SNARE Proteins ; Myristoylated Alanine-Rich C Kinase Substrate (125267-21-2)
    Language English
    Publishing date 2007-09
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 603252-7
    ISSN 0020-1324 ; 0098-9142
    ISSN 0020-1324 ; 0098-9142
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Mucoactive agents for airway mucus hypersecretory diseases.

    Rogers, Duncan F

    Respiratory care

    2007  Volume 52, Issue 9, Page(s) 1176–93; discussion 1193–7

    Abstract: Airway mucus hypersecretion is a feature of a number of severe respiratory diseases, including asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF). However, each disease has a different airway inflammatory response, with ... ...

    Abstract Airway mucus hypersecretion is a feature of a number of severe respiratory diseases, including asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF). However, each disease has a different airway inflammatory response, with consequent, and presumably linked, mucus hypersecretory phenotype. Thus, it is possible that optimal treatment of the mucus hypersecretory element of each disease should be disease-specific. Nevertheless, mucoactive drugs are a longstanding and popular therapeutic option, and numerous compounds (eg, N-acetylcysteine, erdosteine, and ambroxol) are available for clinical use worldwide. However, rational recommendation of these drugs in guidelines for management of asthma, COPD, or CF has been hampered by lack of information from well-designed clinical trials. In addition, the mechanism of action of most of these drugs is unknown. Consequently, although it is possible to categorize them according to putative mechanisms of action, as expectorants (aid and/or induce cough), mucolytics (thin mucus), mucokinetics (facilitate cough transportability), and mucoregulators (suppress mechanisms underlying chronic mucus hypersecretion, such as glucocorticosteroids), it is likely that any beneficial effects are due to activities other than, or in addition to, effects on mucus. It is also noteworthy that the mucus factors that favor mucociliary transport (eg, thin mucus gel layer, "ideal" sol depth, and elasticity greater than viscosity) are opposite to those that favor cough effectiveness (thick mucus layer, excessive sol height, and viscosity greater than elasticity), which indicates that different mucoactive drugs would be required for treatment of mucus obstruction in proximal versus distal airways, or in patients with an impaired cough reflex. With the exception of mucoregulatory agents, whose primary action is unlikely to be directed against mucus, well-designed clinical trials are required to unequivocally determine the effectiveness, or otherwise, of expectorant, mucolytic, and mucokinetic agents in airway diseases in which mucus hypersecretion is a pathophysiological and clinical issue. It is noteworthy that, of the more complex molecules in development, it is simple inhaled hypertonic saline that is currently receiving the greatest attention as a mucus therapy, primarily in CF.
    MeSH term(s) Bronchi/drug effects ; Bronchi/physiology ; Bronchi/physiopathology ; Cough/drug therapy ; Expectorants/pharmacology ; Expectorants/therapeutic use ; Female ; Humans ; Male ; Mucus/drug effects ; Mucus/physiology ; Mucus/secretion ; Respiratory Mucosa/drug effects ; Respiratory Mucosa/physiology ; Respiratory Mucosa/secretion ; Respiratory System/drug effects ; Respiratory System/physiopathology ; Sputum ; Treatment Outcome
    Chemical Substances Expectorants
    Language English
    Publishing date 2007-09
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 603252-7
    ISSN 0020-1324 ; 0098-9142
    ISSN 0020-1324 ; 0098-9142
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Novel Therapies to Inhibit Mucus Synthesis and Secretion in Airway Hypersecretory Diseases.

    Ha, Emily V S / Rogers, Duncan F

    Pharmacology

    2016  Volume 97, Issue 1-2, Page(s) 84–100

    Abstract: Background: In asthma and chronic obstructive pulmonary disease (COPD), airway mucus hypersecretion contributes to impaired mucociliary clearance, mucostasis and, potentially, the development of mucus plugging of the airways.: Summary: Excess mucus ... ...

    Abstract Background: In asthma and chronic obstructive pulmonary disease (COPD), airway mucus hypersecretion contributes to impaired mucociliary clearance, mucostasis and, potentially, the development of mucus plugging of the airways.
    Summary: Excess mucus production can be targeted via therapies that focus on inhibition mucin synthesis, via reducing expression of mucin (MUC) genes, and/or inhibition of mucin secretion into the airways.
    Key messages: This review discusses a number of therapeutic approaches to reduce airway mucus in asthma and COPD, including the use of synthetic and natural products. In particular, it highlights areas where clinical trials of inhibitors of particular target molecules are lacking. Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors are an example of a targeted therapy that has been researched to reduce mucus synthesis, as have inhibitors of EGFR's downstream signalling pathways, for example, mitogen-activated protein kinase-13 and hypoxia inducible factor-1. However, their efficacy and safety profiles are currently not up to the mark. There is clinical potential in Bio-11006, which reduces mucus secretion via the inhibition of myristoylated alanine-rich C-kinase substrate and is currently in Phase IIb trial.
    MeSH term(s) Airway Remodeling/physiology ; Asthma/physiopathology ; Chloride Channels/antagonists & inhibitors ; Ellagic Acid/pharmacology ; GABA Antagonists ; Ginkgolides/pharmacology ; HSP70 Heat-Shock Proteins/antagonists & inhibitors ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology ; Hypoxia-Inducible Factor 1/antagonists & inhibitors ; Inflammation Mediators/metabolism ; Intracellular Signaling Peptides and Proteins/metabolism ; Lactones/pharmacology ; Macrolides/pharmacology ; Membrane Proteins/metabolism ; Mitogen-Activated Protein Kinase 13/antagonists & inhibitors ; Mucins/antagonists & inhibitors ; Mucins/biosynthesis ; Mucus/drug effects ; Mucus/secretion ; Munc18 Proteins/antagonists & inhibitors ; Myristoylated Alanine-Rich C Kinase Substrate ; Protein-Tyrosine Kinases/antagonists & inhibitors ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Receptor, Epidermal Growth Factor/antagonists & inhibitors ; Receptors, Purinergic P2Y
    Chemical Substances CLCA1 protein, human ; Chloride Channels ; GABA Antagonists ; Ginkgolides ; HSP70 Heat-Shock Proteins ; Hydroxymethylglutaryl-CoA Reductase Inhibitors ; Hypoxia-Inducible Factor 1 ; Inflammation Mediators ; Intracellular Signaling Peptides and Proteins ; Lactones ; Macrolides ; Membrane Proteins ; Mucins ; Munc18 Proteins ; Receptors, Purinergic P2Y ; Myristoylated Alanine-Rich C Kinase Substrate (125267-21-2) ; Ellagic Acid (19YRN3ZS9P) ; ginkgolide B (DF149B9460) ; Mitogen-Activated Protein Kinase 13 (EC 2.7.1.-) ; Protein-Tyrosine Kinases (EC 2.7.10.1) ; Receptor, Epidermal Growth Factor (EC 2.7.10.1)
    Language English
    Publishing date 2016
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 206671-3
    ISSN 1423-0313 ; 0031-7012
    ISSN (online) 1423-0313
    ISSN 0031-7012
    DOI 10.1159/000442794
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The role of airway secretions in COPD: pathophysiology, epidemiology and pharmacotherapeutic options.

    Rogers, Duncan F

    COPD

    2006  Volume 2, Issue 3, Page(s) 341–353

    Abstract: Often considered an aggravating but otherwise benign component of chronic obstructive pulmonary disease (COPD), airway mucus hypersecretion is now recognised as a potential risk factor for an accelerated loss of lung function in COPD and is a key ... ...

    Abstract Often considered an aggravating but otherwise benign component of chronic obstructive pulmonary disease (COPD), airway mucus hypersecretion is now recognised as a potential risk factor for an accelerated loss of lung function in COPD and is a key pathophysiological feature in many patients, particularly those prone to respiratory tract infection. Consequently, it is important to develop drugs that inhibit mucus hypersecretion in these susceptible patients. Conventional therapy including anticholinergics, beta2-adrenoceoptor agonists, alone or in combination with corticosteroids, mucolytics and macrolide antibiotics are not entirely or consistently effective in inhibiting airway mucus hypersecretion in COPD. Novel pharmacotherapeutic targets are being investigated, including inhibitors of nerve activity (e.g., BK(Ca) channel activators), tachykinin receptor antagonists, epoxygenase inducers (e.g., benzafibrate), inhibitors of mucin exocytosis (e.g., anti-MARCKS peptide and Munc-18B blockers), inhibitors of mucin synthesis and goblet cell hyperplasia (e.g., EGF receptor tyrosine kinase inhibitors, p38 MAP kinase inhibitors, MEK/ERK inhibitors, hCACL2 blockers and retinoic acid receptor-alpha antagonists), inducers of goblet cell apoptosis (e.g., Bax inducers or Bcl-2 inhibitors), and purinoceptor P(2Y2) antagonists to inhibit mucin secretion or P(2Y2) agonists to hydrate secretions. However, real and theoretical differences delineate the mucus hypersecretory phenotype in COPD from that in other hypersecretory diseases of the airways. More information is required on these differences to identify therapeutic targets pertinent to COPD which, in turn, should lead to rational design of anti-hypersecretory drugs for specific treatment of airway mucus hypersecretion in COPD.
    MeSH term(s) Humans ; Mucus/drug effects ; Mucus/metabolism ; Pulmonary Disease, Chronic Obstructive/drug therapy ; Pulmonary Disease, Chronic Obstructive/epidemiology ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Respiratory Mucosa/drug effects ; Respiratory Mucosa/metabolism ; Respiratory System Agents/therapeutic use ; Sputum/drug effects ; Sputum/metabolism
    Chemical Substances Respiratory System Agents
    Language English
    Publishing date 2006-11-28
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2171107-0
    ISSN 1541-2555
    ISSN 1541-2555
    DOI 10.1080/15412550500218098
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Mucociliary dysfunction in COPD: effect of current pharmacotherapeutic options.

    Rogers, Duncan F

    Pulmonary pharmacology & therapeutics

    2005  Volume 18, Issue 1, Page(s) 1–8

    Abstract: Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality worldwide. COPD comprises multiple components which, as well as a systemic component, include pulmonary inflammation, airway remodelling and mucociliary dysfunction. ...

    Abstract Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality worldwide. COPD comprises multiple components which, as well as a systemic component, include pulmonary inflammation, airway remodelling and mucociliary dysfunction. The latter features contribute to the development of chronic, progressive airflow limitation. The mucociliary dysfunction component of COPD is due to mucus hypersecretion coupled with a decrease in mucus transport, and represents an important pathophysiological feature requiring appropriate treatment. Current international guidelines do not recommend the use of mucolytics in the treatment of stable COPD. In contrast, bronchodilators are central to symptomatic management of COPD, and include beta(2)-adrenoceptor agonists, anti-cholinergics and methylxanthines. Interestingly, long-acting beta(2)-agonists (LABAs), rather than short-acting beta(2)-agonists, have the potential to improve the mucociliary component of COPD, in addition to providing symptomatic treatment by their bronchodilator action. Combination therapy with a LABA and an inhaled corticosteroid has the potential to more fully address the multicomponent nature of COPD by providing important anti-inflammatory activity, which may indirectly further improve mucociliary clearance. Theoretically, anti-cholinergics are likely to have mixed effects on mucociliary function, but clinically these effects have been difficult to demonstrate. Finally, a number of novel targets for the treatment of airway mucociliary dysfunction have been identified, and targeting agents are currently in development.
    MeSH term(s) Adrenergic beta-Agonists/therapeutic use ; Cholinergic Antagonists/therapeutic use ; Humans ; Pulmonary Disease, Chronic Obstructive/drug therapy ; Pulmonary Disease, Chronic Obstructive/etiology ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Respiratory Mucosa/physiopathology
    Chemical Substances Adrenergic beta-Agonists ; Cholinergic Antagonists
    Language English
    Publishing date 2005
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1399707-5
    ISSN 1522-9629 ; 1094-5539
    ISSN (online) 1522-9629
    ISSN 1094-5539
    DOI 10.1016/j.pupt.2004.08.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Therapeutic Options for Hydrating Airway Mucus in Cystic Fibrosis

    Tildy, Bernadett E. / Rogers, Duncan F.

    Pharmacology

    2015  Volume 95, Issue 3-4, Page(s) 117–132

    Abstract: Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the ... ...

    Institution Imperial College London, and National Heart and Lung Institute, Imperial College London, London, UK
    Abstract Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the airway surface liquid due to associated reduced water efflux. PCL layer dehydration reduces mucociliary clearance (MCC), leading to airway obstruction (reduced airflow and inflammation due to pathogen invasion) with mucus plug formation. Summary: Rehydrating mucus increases MCC. Mucus hydration can be achieved by direct hydration (administering osmotic agents to set up an osmotic gradient), using CFTR modulators to correct dysfunctional CFTR, or it can be achieved pharmacologically (targeting other ion channels on airway epithelial cells). Key Messages: The molecular mechanisms of several therapies are discussed in the context of pre-clinical and clinical trial studies. Currently, only the osmotic agent 7% hypertonic saline and the CFTR ‘potentiator' VX-770 (ivacaftor) are used clinically to hydrate mucus. Emerging therapies include the osmotic agent mannitol (Bronchitol), the intracellular Ca2+-raising agent Moli1901/lancovutide, the CFTR potentiator sildenafil [phosphodiesterase type 5 (PDE5) inhibitor] and the CFTR ‘corrector' VX-809 (lumacaftor). Other CFTR correctors (e.g. ‘chemical chaperones') are also showing pre-clinical promise.
    Keywords Mucus ; Lung ; Cystic fibrosis ; Cystic fibrosis transmembrane conductance regulator gene ; Hypertonic saline ; Ivacaftor ; Bronchitol ; Mannitol ; Mucus hydration ; Moli1901
    Language English
    Publishing date 2015-03-19
    Publisher S. Karger AG
    Publishing place Basel, Switzerland
    Document type Article
    Note Review
    ZDB-ID 206671-3
    ISSN 1423-0313 ; 0031-7012
    ISSN (online) 1423-0313
    ISSN 0031-7012
    DOI 10.1159/000377638
    Database Karger publisher's database

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  10. Article ; Online: Therapeutic Options for Hydrating Airway Mucus in Cystic Fibrosis

    Tildy, Bernadett E. / Rogers, Duncan F.

    Pharmacology - International Journal of Experimental and Clinical Pharmacology

    2015  Volume 95, Issue 3-4, Page(s) 117–132

    Abstract: Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the ... ...

    Abstract Background: In cystic fibrosis (CF), genetic mutations in the CF transmembrane conductance regulator (CFTR) gene cause reduced chloride efflux from ciliated airway epithelial cells. This results in a reduction in periciliary liquid (PCL) depth of the airway surface liquid due to associated reduced water efflux. PCL layer dehydration reduces mucociliary clearance (MCC), leading to airway obstruction (reduced airflow and inflammation due to pathogen invasion) with mucus plug formation. Summary: Rehydrating mucus increases MCC. Mucus hydration can be achieved by direct hydration (administering osmotic agents to set up an osmotic gradient), using CFTR modulators to correct dysfunctional CFTR, or it can be achieved pharmacologically (targeting other ion channels on airway epithelial cells). Key Messages: The molecular mechanisms of several therapies are discussed in the context of pre-clinical and clinical trial studies. Currently, only the osmotic agent 7% hypertonic saline and the CFTR ‘potentiator' VX-770 (ivacaftor) are used clinically to hydrate mucus. Emerging therapies include the osmotic agent mannitol (Bronchitol), the intracellular Ca2+-raising agent Moli1901/lancovutide, the CFTR potentiator sildenafil [phosphodiesterase type 5 (PDE5) inhibitor] and the CFTR ‘corrector' VX-809 (lumacaftor). Other CFTR correctors (e.g. ‘chemical chaperones') are also showing pre-clinical promise.© 2015 S. Karger AG, Basel
    Keywords Mucus ; Lung ; Cystic fibrosis ; Cystic fibrosis transmembrane conductance regulator gene ; Hypertonic saline ; Ivacaftor ; Bronchitol ; Mannitol ; Mucus hydration ; Moli1901
    Language English
    Publisher S. Karger AG
    Publishing place Basel
    Publishing country Switzerland
    Document type Article ; Online
    ZDB-ID 206671-3
    ISSN 1423-0313 ; 0031-7012 ; 0031-7012
    ISSN (online) 1423-0313
    ISSN 0031-7012
    DOI 10.1159/000377638
    Database Karger publisher's database

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