Literature DB >> 16357366

Restoration of mucociliary transport in the fluid-depleted trachea by surface-active instillates.

Stephen T Ballard1, James C Parker, Charles R Hamm.   

Abstract

Severe impairment of mucociliary transport (MCT) is a hallmark of cystic fibrosis (CF) lung disease. Recent studies demonstrate that pharmacologic inhibition of anion and liquid secretion in pig tracheas models the MCT defect in CF through depletion of the periciliary fluid component of airway surface liquid. In the present study, the effectiveness of various aqueous instillates on rehydration of the airway surface and restoration of MCT was assessed in this model. Excised porcine tracheas were mounted in a chamber that permitted simultaneous measurement of MCT and adventitial exposure of the airways to Krebs solution. When anion and liquid secretion were inhibited by treatment with bumetanide and dimethylamiloride, MCT was greatly reduced. Luminal instillation of aqueous solutions containing surface-active substances (1% Tween80 or calfactant) transiently restored MCT to high rates in nearly all tissues. Mucosal treatment with only Krebs solution or hypertonic saline restored MCT in only one half of the tracheas. We conclude that aqueous salt solutions alone can hydrate airway surfaces and restore MCT in some tissues, but surface-active substances may provide additional benefit in restoring MCT in this model of mucociliary stasis. We speculate that administration of surface-active substances, by aerosol or lavage, might help to restore MCT in the airways of patients with CF.

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Year:  2005        PMID: 16357366      PMCID: PMC2644211          DOI: 10.1165/rcmb.2005-0214OC

Source DB:  PubMed          Journal:  Am J Respir Cell Mol Biol        ISSN: 1044-1549            Impact factor:   6.914


  28 in total

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Authors:  P J Wills; R L Hall; W Chan; P J Cole
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2.  Nasal mucociliary transport and ciliary ultrastructure in cystic fibrosis. A comparative study with healthy volunteers.

Authors:  M Armengot; A Escribano; C Carda; C Sánchez; C Romero; J Basterra
Journal:  Int J Pediatr Otorhinolaryngol       Date:  1997-05-04       Impact factor: 1.675

3.  Inhibition of airway liquid secretion and its effect on the physical properties of airway mucus.

Authors:  L Trout; M King; W Feng; S K Inglis; S T Ballard
Journal:  Am J Physiol       Date:  1998-02

4.  Surface hydrophobicity is increased in the ileum and proximal colon of cystic fibrosis mice.

Authors:  C Chung; L van Hoof; Z Policova; S Beharry; P M Sherman; A W Neumann; P Durie
Journal:  Pediatr Res       Date:  1999-08       Impact factor: 3.756

5.  Effect of increasing doses of hypertonic saline on mucociliary clearance in patients with cystic fibrosis.

Authors:  M Robinson; A L Hemming; J A Regnis; A G Wong; D L Bailey; G J Bautovich; M King; P T Bye
Journal:  Thorax       Date:  1997-10       Impact factor: 9.139

6.  Effects of aerosolized surfactant in patients with stable chronic bronchitis: a prospective randomized controlled trial.

Authors:  A Anzueto; A Jubran; J A Ohar; C A Piquette; S I Rennard; G Colice; E N Pattishall; J Barrett; M Engle; K A Perret; B K Rubin
Journal:  JAMA       Date:  1997-11-05       Impact factor: 56.272

7.  CFTR as a cAMP-dependent regulator of sodium channels.

Authors:  M J Stutts; C M Canessa; J C Olsen; M Hamrick; J A Cohn; B C Rossier; R C Boucher
Journal:  Science       Date:  1995-08-11       Impact factor: 47.728

8.  Distearoyl phosphatidylglycerol liposomes improve surface and transport properties of CF mucus.

Authors:  S Girod de Bentzmann; D Pierrot; C Fuchey; J M Zahm; J L Morançais; E Puchelle
Journal:  Eur Respir J       Date:  1993-09       Impact factor: 16.671

9.  Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease.

Authors:  H Matsui; B R Grubb; R Tarran; S H Randell; J T Gatzy; C W Davis; R C Boucher
Journal:  Cell       Date:  1998-12-23       Impact factor: 41.582

10.  Submucosal glands are the predominant site of CFTR expression in the human bronchus.

Authors:  J F Engelhardt; J R Yankaskas; S A Ernst; Y Yang; C R Marino; R C Boucher; J A Cohn; J M Wilson
Journal:  Nat Genet       Date:  1992-11       Impact factor: 38.330

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  12 in total

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Authors:  Timothy E Corcoran; Kristina M Thomas; Stephen Garoff; Robert D Tilton; Todd M Przybycien; Joseph M Pilewski
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2.  Buffer drains and mucus is transported upward in a tilted mucus clearance assay.

Authors:  Jerome Carpenter; Suzanne E Lynch; Jeremy A Cribb; Schuyler Kylstra; David B Hill; Richard Superfine
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-09-13       Impact factor: 5.464

3.  Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways.

Authors:  Lubna H Abdullah; Jessica R Evans; T Tiffany Wang; Amina A Ford; Alexander M Makhov; Kristine Nguyen; Raymond D Coakley; Jack D Griffith; C William Davis; Stephen T Ballard; Mehmet Kesimer
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4.  SPLUNC1/BPIFA1 contributes to pulmonary host defense against Klebsiella pneumoniae respiratory infection.

Authors:  Yang Liu; Jennifer A Bartlett; Marissa E Di; Jennifer M Bomberger; Yvonne R Chan; Lokesh Gakhar; Rama K Mallampalli; Paul B McCray; Y Peter Di
Journal:  Am J Pathol       Date:  2013-03-15       Impact factor: 4.307

5.  Mucociliary transport in porcine trachea: differential effects of inhibiting chloride and bicarbonate secretion.

Authors:  Jeffrey L Cooper; Paul M Quinton; Stephen T Ballard
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2012-11-30       Impact factor: 5.464

Review 6.  The porcine lung as a potential model for cystic fibrosis.

Authors:  Christopher S Rogers; William M Abraham; Kim A Brogden; John F Engelhardt; John T Fisher; Paul B McCray; Geoffrey McLennan; David K Meyerholz; Eman Namati; Lynda S Ostedgaard; Randall S Prather; Juan R Sabater; David Anthony Stoltz; Joseph Zabner; Michael J Welsh
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2008-05-16       Impact factor: 5.464

7.  PATHOPHYSIOLOGIC EVALUATION OF THE TRANSGENIC CFTR "GUT-CORRECTED" PORCINE MODEL OF CYSTIC FIBROSIS.

Authors:  Stephen T Ballard; Jessica W Evans; Holly S Drag; Michele Schuler
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2016-08-19       Impact factor: 5.464

8.  Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs.

Authors:  Mark J Hoegger; Maged Awadalla; Eman Namati; Omar A Itani; Anthony J Fischer; Alexander J Tucker; Ryan J Adam; Geoffrey McLennan; Eric A Hoffman; David A Stoltz; Michael J Welsh
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-28       Impact factor: 11.205

9.  Non-invasive airway health assessment: synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo.

Authors:  Martin Donnelley; Kaye S Morgan; Karen K W Siu; Nigel R Farrow; Charlene S Stahr; Richard C Boucher; Andreas Fouras; David W Parsons
Journal:  Sci Rep       Date:  2014-01-14       Impact factor: 4.379

10.  Increased susceptibility to otitis media in a Splunc1-deficient mouse model.

Authors:  Jennifer A Bartlett; David K Meyerholz; Christine L Wohlford-Lenane; Paul W Naumann; Nita H Salzman; Paul B McCray
Journal:  Dis Model Mech       Date:  2015-03-12       Impact factor: 5.758

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