Literature DB >> 3498819

Effect of chloride ions on giant miniature end-plate potentials at the frog neuromuscular junction.

P C Molenaar1, B S Oen, R L Polak.   

Abstract

1. Frog sartorius muscles were incubated in Ringer solutions with a raised K+ concentration (high K+) and then allowed to recover in medium with a normal K+ concentration. During the recovery period miniature end-plate potentials (m.e.p.p.s) were recorded with intracellular electrodes. In addition, the acetylcholine (ACh) released from muscles in the presence of high K+ was measured by a mass spectrometric method. 2. Incubation in a high-K+ medium induced the appearance of giant miniature end-plate potentials (g.m.e.p.p.s). However, if the Cl- of the medium was substituted by propionate, very few g.m.e.p.p.s were observed. This was due to the absence of Cl- and not to the presence of propionate. The frequency of g.m.e.p.p.s was also greatly depressed when the Cl- concentration was lowered from 120 to 60 mM. 3. The amount of ACh released into a high-K+ medium was the same, regardless of whether Cl- or propionate was the anion. 4. When Cl- was replaced by NO3- or Br-, incubation in high-K+ Ringer solution induced the appearance of g.m.e.p.p.s. However, SO4(2-), like propionate, was unable to substitute for Cl- in this respect. 5. The frequency of g.m.e.p.p.s was correlated with that of m.e.p.p.s during the recovery period. However, when the K+ concentration was raised to 17 mM the frequency of m.e.p.p.s greatly increased, whereas that of the g.m.e.p.p.s did not change significantly. 6. G.m.e.p.p.s disappeared in the presence of curare, but persisted in the presence of tetrodotoxin or in a Ca2+-lacking medium. However, g.m.e.p.p.s failed to appear when the medium had lacked Ca2+ during the stimulation. 7. It is tentatively concluded that g.m.e.p.p.s are associated with Cl--dependent processes which occur after stimulation of transmitter release, and which are linked with the endocytotic retrieval of presynaptic membrane.

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Year:  1987        PMID: 3498819      PMCID: PMC1183062          DOI: 10.1113/jphysiol.1987.sp016401

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


  19 in total

1.  The influence of potassium and chloride ions on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

2.  Reversible depletion of synaptic vesicles induced by application of high external potassium to the frog neuromuscular junction.

Authors:  J F Gennaro; W L Nastuk; D T Rutherford
Journal:  J Physiol       Date:  1978-07       Impact factor: 5.182

3.  Proceedings: A possible origin of the 'giant' spontaneous potentials that occur after prolonged transmitter release at frog neuromuscular junctions.

Authors:  J E Heuser
Journal:  J Physiol       Date:  1974-06       Impact factor: 5.182

4.  A method for determination of acetylcholine by slow pyrolysis combined with mass fragmentography on a packed capillary column.

Authors:  R L Polak; P C Molenaar
Journal:  J Neurochem       Date:  1979-02       Impact factor: 5.372

5.  Transmitter release induced by injection of calcium ions into nerve terminals.

Authors:  R Miledi
Journal:  Proc R Soc Lond B Biol Sci       Date:  1973-07-03

6.  On the role of mitochondria in transmitter release from motor nerve terminals.

Authors:  E Alnaes; R Rahamimoff
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

7.  Action of vinblastine on the spontaneous release of acetylcholine at the frog neuromuscular junction.

Authors:  M Pécot-Dechavassine
Journal:  J Physiol       Date:  1976-09       Impact factor: 5.182

8.  The effect of lanthanum ions on acetylcholine in frog muscle.

Authors:  R Miledi; P C Molenaar; R L Polak
Journal:  J Physiol       Date:  1980-12       Impact factor: 5.182

9.  Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction.

Authors:  J E Heuser; T S Reese
Journal:  J Cell Biol       Date:  1973-05       Impact factor: 10.539

10.  Structural changes after transmitter release at the frog neuromuscular junction.

Authors:  J E Heuser; T S Reese
Journal:  J Cell Biol       Date:  1981-03       Impact factor: 10.539

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  6 in total

1.  The effect of anions on bound acetylcholine in frog sartorius muscle.

Authors:  B Ceccarelli; P C Molenaar; B S Oen; R L Polak; F Torri-Tarelli; G T van Kempen
Journal:  J Physiol       Date:  1989-01       Impact factor: 5.182

2.  Analysis of quantal acetylcholine noise at end-plates of frog muscle during rapid transmitter secretion.

Authors:  P C Molenaar; B S Oen
Journal:  J Physiol       Date:  1988-06       Impact factor: 5.182

3.  Giant miniature end-plate potentials at the untreated and emetine-treated frog neuromuscular junction.

Authors:  K A Alkadhi
Journal:  J Physiol       Date:  1989-05       Impact factor: 5.182

4.  Early induction by crotoxin of biphasic frequency changes and giant miniature endplate potentials in frog muscle.

Authors:  B J Hawgood; I C Smith; P N Strong
Journal:  Br J Pharmacol       Date:  1988-07       Impact factor: 8.739

5.  Increasing quantal size at the mouse neuromuscular junction and the role of choline.

Authors:  S P Yu; W Van der Kloot
Journal:  J Physiol       Date:  1991-02       Impact factor: 5.182

6.  Spontaneous release of multiquantal miniature excitatory junction potentials induced by a Drosophila mutant.

Authors:  K Ikeda; J H Koenig
Journal:  J Physiol       Date:  1988-12       Impact factor: 5.182

  6 in total

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