Literature DB >> 6843595

Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis.

P M Quinton, J Bijman.   

Abstract

Patients with cystic fibrosis have characteristic disturbances in the electrolyte composition of their sweat, saliva, and pancreatic secretions. We studied the electrical properties of sweat glands in eight patients with cystic fibrosis and in seven normal volunteers to determine the basis of the well-documented inhibition of sodium absorption in this disease. The average electrical potential across 47 sweat glands in the patients was -66.3 +/- 2.1 mV, as compared with -29.8 +/- 3.2 mV for 39 glands in the normal controls (P less than 0.001). The average sweat-secretion rate in 33 glands from six patients was not significantly different from that in 34 glands from six controls, but average concentrations of sodium, chloride, and potassium were significantly higher in sweat droplets from the patients. Calculated rates of both sodium and chloride reabsorption were lower in sweat glands of patients than of normal controls, but chloride reabsorption was more markedly reduced than sodium reabsorption. We conclude that a decrease in epithelial permeability to chloride may explain the characteristic changes in sweat electrolytes in cystic fibrosis and could be a generalized abnormality in the disease.

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Year:  1983        PMID: 6843595     DOI: 10.1056/NEJM198305193082002

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  46 in total

Review 1.  Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis.

Authors:  Paul M Quinton
Journal:  Am J Physiol Cell Physiol       Date:  2010-10-06       Impact factor: 4.249

2.  Characterization of human sweat duct chloride conductance by chloride channel blockers.

Authors:  J Bijman; H C Englert; H J Lang; R Greger; E Frömter
Journal:  Pflugers Arch       Date:  1987-05       Impact factor: 3.657

3.  Cation transport by sweat ducts in primary culture. Ionic mechanism of cholinergically evoked current oscillations.

Authors:  E H Larsen; I Novak; P S Pedersen
Journal:  J Physiol       Date:  1990-05       Impact factor: 5.182

4.  Low abundance of sweat duct Cl- channel CFTR in both healthy and cystic fibrosis athletes with exceptionally salty sweat during exercise.

Authors:  Mary Beth Brown; Karla K V Haack; Brian P Pollack; Mindy Millard-Stafford; Nael A McCarty
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-01-12       Impact factor: 3.619

5.  Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8.

Authors:  M C Iannuzzi; M Dean; M L Drumm; N Hidaka; J L Cole; A Perry; C Stewart; B Gerrard; F S Collins
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

6.  Cystic fibrosis carrier detection using a linked gene probe.

Authors:  M Farrall; P Scambler; K W Klinger; K Davies; C Worrall; R Williamson; B Wainwright
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

7.  Characterization of two distinct Cl- conductances in fused human respiratory epithelial cells. II. Relation to cystic fibrosis gene product.

Authors:  U H Schröder; E Frömter
Journal:  Pflugers Arch       Date:  1995-06       Impact factor: 3.657

Review 8.  Sinusitis in patients with cystic fibrosis.

Authors:  Y Hui; R Gaffney; W S Crysdale
Journal:  Eur Arch Otorhinolaryngol       Date:  1995       Impact factor: 2.503

Review 9.  Cystic fibrosis: exploiting its genetic basis in the hunt for new therapies.

Authors:  James L Kreindler
Journal:  Pharmacol Ther       Date:  2009-11-10       Impact factor: 12.310

10.  Permeability properties of cell membranes and tight junctions of normal and cystic fibrosis sweat ducts.

Authors:  J Bijman; P Quinton
Journal:  Pflugers Arch       Date:  1987-05       Impact factor: 3.657

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