Literature DB >> 6624917

A transcellular route for Na-coupled Cl transport in secreting pancreatic acinar cells.

J O'Doherty, R J Stark.   

Abstract

Ion-selective microelectrodes were employed to determine the electrochemical driving forces involved in the transepithelial transport of Na+ and Cl- during acetylcholine (ACh) stimulation of pancreatic acinar cells. In HCO-3-free Ringer solution, the mean values of intracellular Cl and Na activities (aiCl and aiNa) were 68.9 +/- 1.1 and 8.3 +/- 0.3 mM, respectively. The mean value of aiCl is above the calculated equilibrium value, indicating that Cl entry into the cell is an energy-requiring process. Continuous measurement of intracellular electrode potentials during stimulation of the cells with concentrations of ACh ranging from 10(-7) to 10(-5) M demonstrated the neurotransmitter's influence on transmembrane Na+ and Cl- movement in secreting cells. The mean values of the induced changes in aiCl and aiNa at every concentration of ACh measured were not significantly different (P greater than 0.5), although the mean changes in either aiNa or aiCl determined with every decade change in ACh concentration were significant (P less than 0.05). The transmembrane Na+ electrochemical gradient dissipated with the induced increases in aiCl. These results suggest that, during stimulus-secretion coupling of pancreatic acinar cells, there is a transcellular route for NaCl secretion, and the energy for NaCl entry into the cell may be derived from the Na+ electrochemical gradient that exists across the basolateral epithelial membrane. They also suggest that the ACh-induced changes in ionic permeability of the plasma membrane may be the coupling mechanism by which the simultaneous events enzyme release and electrolyte secretion are controlled in stimulated cells.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6624917     DOI: 10.1152/ajpgi.1983.245.4.G499

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  10 in total

1.  Stimulation-associated redistribution of Na,K-ATPase in rat lacrimal gland.

Authors:  S C Yiu; R W Lambert; M E Bradley; C E Ingham; K L Hales; R L Wood; A K Mircheff
Journal:  J Membr Biol       Date:  1988-06       Impact factor: 1.843

2.  Different time courses of GTP[gamma-S]-induced exocytosis and current oscillations in isolated mouse pancreatic acinar cells.

Authors:  A Schmid; I Schulz
Journal:  Pflugers Arch       Date:  1996-09       Impact factor: 3.657

3.  Secretagogue and second messenger-activated Cl- permeabilities in isolated pancreatic zymogen granules.

Authors:  C M Fuller; H H Deetjen; A Piiper; I Schulz
Journal:  Pflugers Arch       Date:  1989-10       Impact factor: 3.657

4.  Acetylcholine-induced change in intracellular Cl- activity of the mouse lacrimal acinar cells.

Authors:  Y Saito; T Ozawa; H Hayashi; A Nishiyama
Journal:  Pflugers Arch       Date:  1985-09       Impact factor: 3.657

5.  The effects of various anions and cations on the regulation of pyruvate dehydrogenase complex activity from pig kidney cortex.

Authors:  T Pawelczyk; R A Easom; M S Olson
Journal:  Biochem J       Date:  1988-08-01       Impact factor: 3.857

6.  Ionic and osmotic dependence of secretion from permeabilised acini of the rat pancreas.

Authors:  C M Fuller; L Eckhardt; I Schulz
Journal:  Pflugers Arch       Date:  1989-02       Impact factor: 3.657

7.  Acetylcholine-induced Na+ influx in the mouse lacrimal gland acinar cells: demonstration of multiple Na+ transport mechanisms by intracellular Na+ activity measurements.

Authors:  Y Saito; T Ozawa; A Nishiyama
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

8.  Na+, K+, and Cl- transport in resting pancreatic acinar cells.

Authors:  H Zhao; S Muallem
Journal:  J Gen Physiol       Date:  1995-12       Impact factor: 4.086

9.  Agonist-specific regulation of [Na+]i in pancreatic acinar cells.

Authors:  H Zhao; S Muallem
Journal:  J Gen Physiol       Date:  1995-12       Impact factor: 4.086

Review 10.  Physiological Processes Modulated by the Chloride-Sensitive WNK-SPAK/OSR1 Kinase Signaling Pathway and the Cation-Coupled Chloride Cotransporters.

Authors:  Adrián Rafael Murillo-de-Ozores; María Chávez-Canales; Paola de Los Heros; Gerardo Gamba; María Castañeda-Bueno
Journal:  Front Physiol       Date:  2020-10-20       Impact factor: 4.566

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.