Literature DB >> 3391365

Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas.

H Kopelman1, M Corey, K Gaskin, P Durie, Z Weizman, G Forstner.   

Abstract

Pancreatic fluid and electrolyte secretion was assessed in 56 patients with cystic fibrosis (CF) and 56 non-CF control subjects undergoing pancreatic function testing while stimulated with cholecystokinin and secretin. Both CF patients and control subjects exhibited a wide range of pancreatic function. Fluid and trypsin outputs were positively correlated in both groups. Fluid output in CF subjects was significantly lower, however, than that of control subjects at any given level of trypsin output. Sodium, bicarbonate, and chloride secretions were all significantly decreased in CF subjects. Bicarbonate and chloride were important determinants of fluid secretion, but at any given bicarbonate or chloride output CF subjects secreted significantly less fluid than control subjects. When bicarbonate and chloride were analyzed as simultaneous predictor variables, adjusted fluid secretion was not significantly different in CF and control subjects. Diminished fluid secretion in CF subjects is therefore caused by impaired chloride, as well as bicarbonate, secretion.

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Year:  1988        PMID: 3391365     DOI: 10.1016/0016-5085(88)90490-8

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  64 in total

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Authors:  Paul M Quinton
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2.  Severe defects in absorptive ion transport in distal colons of mice that lack ClC-2 channels.

Authors:  Marcelo A Catalán; Carlos A Flores; Mireya González-Begne; Yan Zhang; Francisco V Sepúlveda; James E Melvin
Journal:  Gastroenterology       Date:  2011-11-10       Impact factor: 22.682

Review 3.  Cystic fibrosis, pathophysiological and clinical aspects.

Authors:  H J Neijens; M Sinaasappel; R de Groot; J C de Jongste; S E Overbeek
Journal:  Eur J Pediatr       Date:  1990-08       Impact factor: 3.183

Review 4.  Cystic fibrosis. 6. Gastrointestinal and nutritional aspects.

Authors:  H Kopelman
Journal:  Thorax       Date:  1991-04       Impact factor: 9.139

Review 5.  Pathophysiology of the exocrine pancreas in cystic fibrosis.

Authors:  P R Durie; G G Forstner
Journal:  J R Soc Med       Date:  1989       Impact factor: 5.344

6.  Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line.

Authors:  H Kopelman; C Gauthier; M Bornstein
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7.  Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis.

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Journal:  Pflugers Arch       Date:  2004-04-14       Impact factor: 3.657

Review 8.  Interactions of connexins with other membrane channels and transporters.

Authors:  Marc Chanson; Basilio A Kotsias; Camillo Peracchia; Scott M O'Grady
Journal:  Prog Biophys Mol Biol       Date:  2007-03-14       Impact factor: 3.667

9.  Cystic fibrosis-related diabetes: from CFTR dysfunction to oxidative stress.

Authors:  Thierry Ntimbane; Blandine Comte; Geneviève Mailhot; Yves Berthiaume; Vincent Poitout; Marc Prentki; Rémi Rabasa-Lhoret; Emile Levy
Journal:  Clin Biochem Rev       Date:  2009-11

10.  The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct.

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Journal:  J Physiol       Date:  2008-06-19       Impact factor: 5.182

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