Literature DB >> 6620178

Time course of release of catecholamine and other granular contents from perifused adrenal chromaffin cells of guinea-pig.

S Ito.   

Abstract

Experiments were carried out to investigate the time course of the release of catecholamine, dopamine-beta-hydroxylase (DBH) and adenine nucleotides from isolated chromaffin cells of guinea-pig adrenal gland. When the isolated chromaffin cells were incubated with medium containing acetylcholine (ACh) (0.1 mM), veratridine (0.1 mM) or scorpion (Leiurus quinquestriatus) venom, (10 micrograms/ml.), catecholamine was released into the medium. Catecholamine secretion induced by veratridine or scorpion venom was inhibited by tetrodotoxin (1 microM) but not by atropine (0.1 mM) plus hexamethonium (0.1 mM). On the other hand, the secretory response to ACh was abolished by the cholinergic blocking drugs but not by tetrodotoxin. DBH was released together with catecholamine into the medium in which cells were suspended with these drugs. The ratio of catecholamine (n-mole) to DBH activity (n-mole/hr) appearing in the supernatant was 7.08 +/- 0.55, 6.60 +/- 0.27 and 8.91 +/- 0.47 for ACh, veratridine and scorpion venom, respectively. These values were close to that found in the lysate of chromaffin granules obtained from guinea-pig adrenal glands (7.37 +/- 0.39). The application of ACh or veratridine to perifused chromaffin cells was found to cause a parallel increase in catecholamine and DBH secretion in the perifusion medium without corresponding amounts of phenylethanolamine-N-methyltransferase leakage. However, DBH secretion tended to last for a longer period than catecholamine secretion. Adenine nucleotides were released from perifused chromaffin cells together with catecholamine, by ACh and veratridine. ATP added to the perifusion medium was metabolized to ADP and AMP, of which the ratio (ATP, 21.6%; ADP, 34%; AMP, 17.9%) was close to those of adenine nucleotides released from the cells. The secretion of adenine nucleotides induced by both secretagogues ceased much faster than the catecholamine secretion, so that molar ratio of catecholamine to adenine nucleotides was gradually increased during and after stimulation. The results indicate that catecholamine secretion is accompanied with a simultaneous release of DBH and ATP from adrenal chromaffin cells. Therefore, it is suggested that the delayed output of DBH, unlike catecholamine secretion, in perfused adrenal glands results from the presence of a diffusion barrier for this protein. The releasable secretory granules of isolated chromaffin cells are suggested to be heterogeneous with respect to the ratio of catecholamine to ATP.

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Year:  1983        PMID: 6620178      PMCID: PMC1195327          DOI: 10.1113/jphysiol.1983.sp014798

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  43 in total

1.  Tissue fractionation and catecholamines. II. Intracellular distribution patterns of tyrosine hydroxylase, dopa decarboxylase, dopamine-beta-hydroxylase, phenylethanolamine N-methyltransferase and monoamine oxidase in adrenal medulla.

Authors:  P Laduron; F Belpaire
Journal:  Biochem Pharmacol       Date:  1968-07       Impact factor: 5.858

2.  Isolation and characterization of multiple forms of phenylethanolamine N-methyltransferase.

Authors:  T H Joh; M Goldstein
Journal:  Mol Pharmacol       Date:  1973-01       Impact factor: 4.436

3.  Efflux of adenine nucleotides from perfused adrenal glands exposed to nicotine and other chromaffin cell stimulants.

Authors:  W W Douglas; A M Poisner; R P Rubin
Journal:  J Physiol       Date:  1965-07       Impact factor: 5.182

4.  A sensitive enzymatic assay for dopamine- -hydroxylase.

Authors:  P B Molinoff; R Weinshilboum; J Axelrod
Journal:  J Pharmacol Exp Ther       Date:  1971-09       Impact factor: 4.030

5.  On the relation between ATP splitting and secretion in the adrenal chromaffin cell: extrusion of ATP (unhydrolysed) during release of catecholamines.

Authors:  W W Douglas; A M Poisner
Journal:  J Physiol       Date:  1966-03       Impact factor: 5.182

6.  Evidence that the secreting adrenal chromaffin cell releases catecholamines directly from ATP-rich granules.

Authors:  W W Douglas; A M Poisner
Journal:  J Physiol       Date:  1966-03       Impact factor: 5.182

7.  Mechanism of secretion from the adrenal medulla. II. Release of catecholamines and storage vesicle protein in response to chemical stimulation.

Authors:  N Kirshner; H J Sage; W J Smith
Journal:  Mol Pharmacol       Date:  1967-05       Impact factor: 4.436

8.  A simple method for the isolation of adrenal chromaffin granules on a large scale.

Authors:  A D Smith; H Winkler
Journal:  Biochem J       Date:  1967-05       Impact factor: 3.857

9.  Secretion of a chromaffin granule protein, chromogranin, from the adrenal gland after splanchnic stimulation.

Authors:  H Blaschko; R S Comline; F H Schneider; M Silver; A D Smith
Journal:  Nature       Date:  1967-07-01       Impact factor: 49.962

10.  The release of adenosine triphosphate catabolites during the secretion of catecholamines by bovine adrenal medulla.

Authors:  P Banks
Journal:  Biochem J       Date:  1966-11       Impact factor: 3.857

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  4 in total

1.  Modulation of calcium current by ATP in guinea-pig adrenal chromaffin cells.

Authors:  K Otsuguro; T Ohta; S Ito; Y Nakazato
Journal:  Pflugers Arch       Date:  1996-01       Impact factor: 3.657

2.  Facilitation of transmitter action on catecholamine output by cardiac glycoside in perfused adrenal gland of guinea-pig.

Authors:  Y Nakazato; A Ohga; Y Yamada
Journal:  J Physiol       Date:  1986-05       Impact factor: 5.182

3.  Mice overexpressing chromogranin A display hypergranulogenic adrenal glands with attenuated ATP levels contributing to the hypertensive phenotype.

Authors:  Saiful A Mir; Ying Li; Jacob D Story; Soma Bal; Linda Awdishu; Anneke A Street; Ravindra L Mehta; Prabhleen Singh; Sucheta M Vaingankar
Journal:  J Hypertens       Date:  2018-05       Impact factor: 4.844

4.  Characteristics of 5-HT-containing chemoreceptor cells of the chicken aortic body.

Authors:  S Ito; T Ohta; Y Nakazato
Journal:  J Physiol       Date:  1999-02-15       Impact factor: 5.182

  4 in total

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