Literature DB >> 24743971

Quantitative imaging of airway liquid absorption in cystic fibrosis.

Landon W Locke1, Michael M Myerburg1, Matthew R Markovetz2, Robert S Parker2, Lawrence Weber3, Michael R Czachowski4, Thomas J Harding4, Stefanie L Brown1, Joseph A Nero2, Joseph M Pilewski5, Timothy E Corcoran6.   

Abstract

New measures are needed to rapidly assess emerging treatments for cystic fibrosis (CF) lung disease. Using an imaging approach, we evaluated the absorptive clearance of the radiolabeled small molecule probe diethylene triamine penta-acetic acid (DTPA) as an in vivo indicator of changes in airway liquid absorption. DTPA absorption and mucociliary clearance rates were measured in 21 patients with CF (12 adults and nine children) and nine adult controls using nuclear imaging. The effect of hypertonic saline on DTPA absorption was also studied. In addition, in vitro studies were conducted to identify the determinants of transepithelial DTPA absorption. CF patients had significantly increased rates of DTPA absorption compared with control subjects but had similar mucociliary clearance rates. Treatment with hypertonic saline resulted in a decrease in DTPA absorption and an increase in mucociliary clearance in 11 out of 11 adult CF patients compared with treatment with isotonic saline. In vitro studies revealed that ∼ 50% of DTPA absorption can be attributed to transepithelial fluid transport. Apically applied mucus impedes liquid and DTPA absorption. However, mucus effects become negligible in the presence of an osmotic stimulus. Functional imaging of DTPA absorption provides a quantifiable marker of immediate response to treatments that promote airway surface liquid hydration. ©ERS 2014.

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Year:  2014        PMID: 24743971      PMCID: PMC4150848          DOI: 10.1183/09031936.00220513

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  27 in total

1.  UTP inhibits Na+ absorption in wild-type and DeltaF508 CFTR-expressing human bronchial epithelia.

Authors:  D C Devor; J M Pilewski
Journal:  Am J Physiol       Date:  1999-04

Review 2.  Inhaled mannitol for the treatment of cystic fibrosis.

Authors:  Katharine Hurt; Diana Bilton
Journal:  Expert Rev Respir Med       Date:  2012-02       Impact factor: 3.772

3.  Acute regulation of the epithelial sodium channel in airway epithelia by proteases and trafficking.

Authors:  Michael M Myerburg; Peter R Harvey; Elisa M Heidrich; Joseph M Pilewski; Michael B Butterworth
Journal:  Am J Respir Cell Mol Biol       Date:  2010-01-22       Impact factor: 6.914

4.  The effect of inhaled mannitol on bronchial mucus clearance in cystic fibrosis patients: a pilot study.

Authors:  M Robinson; E Daviskas; S Eberl; J Baker; H K Chan; S D Anderson; P T Bye
Journal:  Eur Respir J       Date:  1999-09       Impact factor: 16.671

5.  Mucus clearance and lung function in cystic fibrosis with hypertonic saline.

Authors:  Scott H Donaldson; William D Bennett; Kirby L Zeman; Michael R Knowles; Robert Tarran; Richard C Boucher
Journal:  N Engl J Med       Date:  2006-01-19       Impact factor: 91.245

6.  Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway.

Authors:  T E Corcoran; K M Thomas; M M Myerburg; A Muthukrishnan; L Weber; R Frizzell; J M Pilewski
Journal:  Eur Respir J       Date:  2009-08-28       Impact factor: 16.671

Review 7.  New concepts of the pathogenesis of cystic fibrosis lung disease.

Authors:  R C Boucher
Journal:  Eur Respir J       Date:  2004-01       Impact factor: 16.671

8.  CFTR and tight junctions in cultured bronchial epithelial cells.

Authors:  Harriet E Nilsson; Anca Dragomir; Lucia Lazorova; Marie Johannesson; Godfried M Roomans
Journal:  Exp Mol Pathol       Date:  2009-10-08       Impact factor: 3.362

Review 9.  Mucociliary clearance as an outcome measure for cystic fibrosis clinical research.

Authors:  Scott H Donaldson; Timothy E Corcoran; Beth L Laube; William D Bennett
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

10.  Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner.

Authors:  Paul D W Eckford; Canhui Li; Mohabir Ramjeesingh; Christine E Bear
Journal:  J Biol Chem       Date:  2012-08-31       Impact factor: 5.157

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  13 in total

1.  Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

Authors:  Timothy E Corcoran; Alex S Huber; Michael M Myerburg; Daniel J Weiner; Landon W Locke; Ryan T Lacy; Lawrence Weber; Michael R Czachowski; Darragh J Johnston; Ashok Muthukrishnan; Alison T Lennox; Joseph M Pilewski
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2019-04-10       Impact factor: 2.849

2.  Overnight delivery of hypertonic saline by nasal cannula aerosol for cystic fibrosis.

Authors:  Timothy E Corcoran; Joseph E Godovchik; Karl H Donn; David R Busick; Jennifer Goralski; Landon W Locke; Matthew R Markovetz; Michael M Myerburg; Ashok Muthukrishnan; Lawrence Weber; Ryan T Lacy; Joseph M Pilewski
Journal:  Pediatr Pulmonol       Date:  2017-07-24

3.  Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25-28 March 2015.

Authors:  Alan S Verkman; Aleksander Edelman; Margarida Amaral; Marcus A Mall; Jeffrey M Beekman; Torsten Meiners; Luis J V Galietta; Christine E Bear
Journal:  J Cyst Fibros       Date:  2015-10-21       Impact factor: 5.482

4.  The in vitro effect of nebulised hypertonic saline on human bronchial epithelium.

Authors:  Jennifer L Goralski; Dan Wu; William R Thelin; Richard C Boucher; Brian Button
Journal:  Eur Respir J       Date:  2018-05-17       Impact factor: 16.671

5.  A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia.

Authors:  Florencio Serrano Castillo; Carol A Bertrand; Michael M Myerburg; Monica E Shapiro; Timothy E Corcoran; Robert S Parker
Journal:  J Pharmacokinet Pharmacodyn       Date:  2019-09-07       Impact factor: 2.745

Review 6.  Mucus Hyperconcentration as a Unifying Aspect of the Chronic Bronchitic Phenotype.

Authors:  Brian Button; Wayne H Anderson; Richard C Boucher
Journal:  Ann Am Thorac Soc       Date:  2016-04

7.  Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung.

Authors:  Landon W Locke; Michael M Myerburg; Daniel J Weiner; Matthew R Markovetz; Robert S Parker; Ashok Muthukrishnan; Lawrence Weber; Michael R Czachowski; Ryan T Lacy; Joseph M Pilewski; Timothy E Corcoran
Journal:  Eur Respir J       Date:  2016-03-23       Impact factor: 16.671

8.  Excess mucus viscosity and airway dehydration impact COPD airway clearance.

Authors:  Vivian Y Lin; Niroop Kaza; Susan E Birket; Harrison Kim; Lloyd J Edwards; Jennifer LaFontaine; Linbo Liu; Marina Mazur; Stephen A Byzek; Justin Hanes; Guillermo J Tearney; S Vamsee Raju; Steven M Rowe
Journal:  Eur Respir J       Date:  2020-01-30       Impact factor: 16.671

Review 9.  Osmolytes and ion transport modulators: new strategies for airway surface rehydration.

Authors:  Jennifer L Goralski; Richard C Boucher; Brian Button
Journal:  Curr Opin Pharmacol       Date:  2010-05-01       Impact factor: 5.547

10.  Direct monitoring of pulmonary disease treatment biomarkers using plasmonic gold nanorods with diffusion-sensitive OCT.

Authors:  R L Blackmon; S M Kreda; P R Sears; B S Chapman; D B Hill; J B Tracy; L E Ostrowski; A L Oldenburg
Journal:  Nanoscale       Date:  2017-04-13       Impact factor: 7.790

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