Literature DB >> 562505

Effect of extracellular K+ concentration on resting potential, caerulein-induced depolarization and amylase release from mouse pancreatic acinar cells.

J H Poulsen, J A Williams.   

Abstract

Acinar cell membrane potentials and amylase release were measured from in vitro preparations of mouse pancreas. The effect of a 10-fold increase of the extracellular K+ concentration (to 47 mM) was studied on the resting membrane potential and amylase release as well as on the membrane depolarization and amylase release induced by the cholecystokinin-pancreozymin analogue, caerulein. In the presence of atropine (to exclude the effect of a possible release of endogenous acetylcholine), the increased K+ concentrations depolarized the cells from -45 to -20 mV without influencing the rate of the unstimulated release of amylase. Under these conditions, the depolarizing effect of caerulein was almost abolished, while the caerulein-induced amylase was not. It is concluded that caerulein-induced enzyme secretion from pancreatic acinar cells is independent of the level of the membrane potential as well as extracellular K+ concentration in the range from 4.7--47 mM.

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Year:  1977        PMID: 562505     DOI: 10.1007/bf00581691

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  17 in total

1.  Pancreatic acinar cells: ionic dependence of acetylcholine-induced membrane potential and resistance change.

Authors:  A Nishiyama; O H Petersen
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

2.  Pancreatic acinar cells: use of Ca++ ionophore to separate enzyme release from the earlier steps in stimulus-secretion coupling.

Authors:  J A Williams; M Lee
Journal:  Biochem Biophys Res Commun       Date:  1974-09-23       Impact factor: 3.575

3.  Origin of transmembrane potentials in non-excitable cells.

Authors:  J A Williams
Journal:  J Theor Biol       Date:  1970-08       Impact factor: 2.691

4.  Stimulation of amylase secretion from the perfused cat pancreas by potassium and other alkali metal ions.

Authors:  B E Argent; R M Case; T Scratcherd
Journal:  J Physiol       Date:  1971-08       Impact factor: 5.182

5.  Ca++ and pancreatic amylase release.

Authors:  J A Williams; D Chandler
Journal:  Am J Physiol       Date:  1975-06

6.  Control of pancreatic amylase release in vitro: effects of ions, cyclic AMP, and colchicine.

Authors:  L Benz; B Eckstein; E K Matthews; J A Williams
Journal:  Br J Pharmacol       Date:  1972-09       Impact factor: 8.739

7.  Effects of the calcium ionophore A23187 on pancreatic acinar cell membrane potentials and amylase release.

Authors:  J H Poulsen; J A Williams
Journal:  J Physiol       Date:  1977-01       Impact factor: 5.182

8.  Pancreatic acinar cells: acetylcholine-induced membrane depolarization, calcium efflux and amylase release.

Authors:  E K Matthews; O H Petersen; J A Williams
Journal:  J Physiol       Date:  1973-11       Impact factor: 5.182

9.  Pancreatic acinar cells: ionic dependence of the membrane potential and acetycholine-induced depolarization.

Authors:  E K Matthews; O H Petersen
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

10.  The action of caerulein on pancreatic secretion of the dog and biliary secretion of the dog and the rat.

Authors:  G Bertaccini; G De Caro; R Endean; V Erspamer; M Impicciatore
Journal:  Br J Pharmacol       Date:  1969-09       Impact factor: 8.739

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  4 in total

1.  Simultaneous monitoring of electrical and secretory activity in peptidergic neurosecretory terminals of the crab.

Authors:  E L Stuenkel
Journal:  J Physiol       Date:  1985-02       Impact factor: 5.182

2.  Pancreatic acinar cells: effects of micro-ionophoretic polypeptide application on membrane potential and resistance.

Authors:  O H Petersen; H G Philpott
Journal:  J Physiol       Date:  1979-05       Impact factor: 5.182

3.  Intracellular divalent cation release in pancreatic acinar cells during stimulus-secretion coupling. I. Use of chlorotetracycline as fluorescent probe.

Authors:  D E Chandler; J A Williams
Journal:  J Cell Biol       Date:  1978-02       Impact factor: 10.539

4.  The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis.

Authors:  Wenguang Yin; Hyun-Taek Kim; ShengPeng Wang; Felix Gunawan; Lei Wang; Keishi Kishimoto; Hua Zhong; Dany Roman; Jens Preussner; Stefan Guenther; Viola Graef; Carmen Buettner; Beate Grohmann; Mario Looso; Mitsuru Morimoto; Graeme Mardon; Stefan Offermanns; Didier Y R Stainier
Journal:  Nat Commun       Date:  2018-07-19       Impact factor: 14.919

  4 in total

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