Literature DB >> 6151643

Control of quantal transmitter release at frog's motor nerve terminals. II. Modulation by de- or hyperpolarizing pulses.

J Dudel.   

Abstract

Quanta of transmitter were released from motor nerve terminals of the frog by a depolarizing 'releasing pulse'. 'Modulating pulses' were subthreshold for release; pre-pulses were added directly before and post-pulses directly after the releasing pulse. Modulating depolarization pulses enhanced release up to 20-fold, and such hyperpolarizations suppressed release up to 10-fold. Pre- and post-pulses were about equally effective. In a wide range these modulations did not affect the facilitation of a test-EPSC by the preceding releasing pulse; modulation thus is not mediated by changes in Ca-inflow. It is suggested that phasic release is largely controlled by an 'activator' which is generated by depolarization, and that modulating pulses increase this activator when depolarizing, and decrease this activator below its resting level if hyperpolarizing. If an interval was interposed between pre- and releasing pulse, the modulating effect decreased very steeply with increasing interval for the first 2 ms, and much slower for longer intervals. Distributions of delays of quantal releases showed a time course of decay very similar to the decay of modulation with increasing interval. Both decays may reflect the exponential decay of activator. Depolarizing post-pulses increased the minimal synaptic delay and the delay of maximal release, and hyperpolarizing ones had the opposite effects. They are interpreted to modulate the generation and decay of a 'repressor', which is produced by depolarization and is responsible for the minimal synaptic delay and the delayed maxima of release. A speculative scheme of interactions of [Ca]i, activator and repressor is discussed.

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Year:  1984        PMID: 6151643     DOI: 10.1007/BF00585505

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


  20 in total

1.  The effect of polarizing current on action potential and transmitter release in crayfish motor nerve terminals.

Authors:  J Dudel
Journal:  Pflugers Arch       Date:  1971       Impact factor: 3.657

2.  Modification of transmitter release by electrical interference with motor nerve endings.

Authors:  B Katz; R Miledi
Journal:  Proc R Soc Lond B Biol Sci       Date:  1967-01-31

3.  The effects of depolarization of motor nerve terminals upon the release of transmitter by nerve impulses.

Authors:  J I Hubbard; W D Willis
Journal:  J Physiol       Date:  1968-02       Impact factor: 5.182

4.  Charges and potentials at the nerve surface. Divalent ions and pH.

Authors:  B Hille
Journal:  J Gen Physiol       Date:  1968-02       Impact factor: 4.086

5.  Neurotransmitter release and its facilitation in crayfish muscle. VI. Release determined by both, intracellular calcium concentration and depolarization of the nerve terminal.

Authors:  J Dudel; I Parnas; H Parnas
Journal:  Pflugers Arch       Date:  1983-09       Impact factor: 3.657

6.  Neurotransmitter release mechanisms and microtubules.

Authors:  E G Gray
Journal:  Proc R Soc Lond B Biol Sci       Date:  1983-05-23

7.  Transmitter release triggered by a local depolarization in motor nerve terminals of the frog: role of calcium entry and of depolarization.

Authors:  J Dudel
Journal:  Neurosci Lett       Date:  1983-10-31       Impact factor: 3.046

8.  Relationship between presynaptic calcium current and postsynaptic potential in squid giant synapse.

Authors:  R Llinás; I Z Steinberg; K Walton
Journal:  Biophys J       Date:  1981-03       Impact factor: 4.033

9.  Electronic properties of motor nerve terminals.

Authors:  J Molgó; S Thesleff
Journal:  Acta Physiol Scand       Date:  1982-02

10.  Secretion of acetylcholine in response to graded depolarization of motor nerve terminals.

Authors:  N B Datyner; P W Gage
Journal:  J Physiol (Paris)       Date:  1982
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  20 in total

1.  The timing of phasic transmitter release is Ca2+-dependent and lacks a direct influence of presynaptic membrane potential.

Authors:  Felix Felmy; Erwin Neher; Ralf Schneggenburger
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-20       Impact factor: 11.205

2.  Blockage of synaptic release by brief hyperpolarizing pulses in the neuromuscular junction of the crayfish.

Authors:  H Arechiga; A Cannone; H Parnas; I Parnas
Journal:  J Physiol       Date:  1990-11       Impact factor: 5.182

3.  Neurotransmitter release and its facilitation in crayfish. VII. Another voltage dependent process beside Ca entry controls the time course of phasic release.

Authors:  H Parnas; J Dudel; I Parnas
Journal:  Pflugers Arch       Date:  1986-02       Impact factor: 3.657

4.  Shifts in the voltage dependence of synaptic release due to changes in the extracellular calcium concentration at nerve terminals on muscle of crayfish and frogs.

Authors:  J Dudel
Journal:  Pflugers Arch       Date:  1989-12       Impact factor: 3.657

5.  Calcium dependence of quantal release triggered by graded depolarization pulses to nerve terminals on crayfish and frog muscle.

Authors:  J Dudel
Journal:  Pflugers Arch       Date:  1989-12       Impact factor: 3.657

6.  Twin pulse facilitation in dependence on pulse duration and calcium concentration at motor nerve terminals of crayfish and frogs.

Authors:  J Dudel
Journal:  Pflugers Arch       Date:  1989-12       Impact factor: 3.657

7.  Dependence of double-pulse facilitation on amplitude and duration of the depolarization pulses at frog's motor nerve terminals.

Authors:  J Dudel
Journal:  Pflugers Arch       Date:  1986-05       Impact factor: 3.657

8.  The calcium hypothesis and modulation of transmitter release by hyperpolarizing pulses.

Authors:  R S Zucker
Journal:  Biophys J       Date:  1987-08       Impact factor: 4.033

Review 9.  Neurotransmitter release at fast synapses.

Authors:  H Parnas; I Parnas
Journal:  J Membr Biol       Date:  1994-12       Impact factor: 1.843

10.  Neurotransmitter release: facilitation and three-dimensional diffusion of intracellular calcium.

Authors:  G Hovav; H Parnas; I Parnas
Journal:  Bull Math Biol       Date:  1992-09       Impact factor: 1.758

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