Literature DB >> 3701333

Real-time monitoring of the secretory function of cultured adrenal chromaffin cells.

K Kumakura, M Ohara, G P Satô.   

Abstract

A system to discriminate the real-time dynamics of the secretory function in cultured adrenal chromaffin cells, using a cell bed perfusion technique and an amperometric detector, was established. Examination of basal conditions revealed that the electrode potential and flow rate are crucial factors for monitoring precise dynamics of the secretory process. Stimulation of the cells either with acetylcholine (ACh) or with high K+ concentration caused a transient current response. The current responses showed concentration dependence for both stimuli, and also showed a high correlation with the amount of catecholamines (CA) in the respective peak fraction of perfusate. Either prolonged cholinergic stimulation or maintained depolarization produced a transient response, which is not attributable to a depletion of releasable storage of CA as indicated by double-stimulation experiments. Stimulation with high K+ concentration evoked an additional release of CA even after the cellular response to prolonged ACh was inactivated, whereas maintained depolarization with high K+ produced both facilitatory and inhibitory effects on the cell responsiveness to ACh. Most probably the transient natures of the secretory responses to ACh and to high K+ are mediated by different mechanisms. All the results suggest that the direct monitoring is profitable for studies on the regulatory mechanisms of the secretory function.

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Year:  1986        PMID: 3701333     DOI: 10.1111/j.1471-4159.1986.tb08504.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  9 in total

1.  The quantal secretion of catecholamines is impaired by the accumulation of beta-adrenoceptor antagonists into chromaffin cell vesicles.

Authors:  Mónica S Montesinos; Marcial Camacho; J David Machado; O Humberto Viveros; Beatriz Beltrán; Ricardo Borges
Journal:  Br J Pharmacol       Date:  2010-03-05       Impact factor: 8.739

2.  Nitric oxide participates in the stimulatory and neurotoxic action of endothelin on rat striatal dopaminergic neurons.

Authors:  H Shibaguchi; Y Kataoka; S Koizumi; M Kohzuma; M Obana; A Himeno; K Yamashita; K Taniyama
Journal:  Cell Mol Neurobiol       Date:  1997-10       Impact factor: 5.046

3.  Conformational change and localization of calpactin I complex involved in exocytosis as revealed by quick-freeze, deep-etch electron microscopy and immunocytochemistry.

Authors:  T Nakata; K Sobue; N Hirokawa
Journal:  J Cell Biol       Date:  1990-01       Impact factor: 10.539

4.  Characterization of exocytotic events from single PC12 cells: amperometric studies in native PC12h, DA-loaded PC12h and bovine adrenal chromaffin cells.

Authors:  Nobuyuki Sasakawa; Norie Murayama; Konosuke Kumakura
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

5.  Effects of imidazole compounds on catecholamine release in adrenal chromaffin cells.

Authors:  M Ohara-Imaizumi; K Kumakura
Journal:  Cell Mol Neurobiol       Date:  1992-06       Impact factor: 5.046

6.  Endothelin-3 stimulates inositol 1,4,5-trisphosphate production and Ca2+ influx to produce biphasic dopamine release from rat striatal slices.

Authors:  Y Kataoka; S Koizumi; M Niwa; H Shibaguchi; K Shigematsu; Y Kudo; K Taniyama
Journal:  Cell Mol Neurobiol       Date:  1994-06       Impact factor: 5.046

7.  Modulation of potassium evoked secretory function in rat cerebellar slices measured by real time monitoring: evidence of a possible role for methylfolate in cerebral tissue.

Authors:  M D Lucock; M I Levene; R Hartley
Journal:  Neurochem Res       Date:  1993-05       Impact factor: 3.996

8.  Effect of diadenosine polyphosphates on catecholamine secretion from isolated chromaffin cells.

Authors:  E Castro; M Torres; M T Miras-Portugal; M P Gonzalez
Journal:  Br J Pharmacol       Date:  1990-06       Impact factor: 8.739

9.  Chromostatin, a 20-amino acid peptide derived from chromogranin A, inhibits chromaffin cell secretion.

Authors:  E Galindo; A Rill; M F Bader; D Aunis
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-15       Impact factor: 11.205

  9 in total

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