Literature DB >> 7669892

The rise times of miniature endplate currents suggest that acetylcholine may be released over a period of time.

W Van der Kloot1.   

Abstract

Models of miniature endplate currents predict 20-80% rise times of 100 microseconds or less. These predictions are substantially less than most of the rise times recorded in the literature. New measurements were made of rise times at the frog neuromuscular junction using extracellular recording. The mean 20-80% rise time was 250 microseconds. Rise times were variable; at 20 degrees C, 95% of them fell in a range from 140 to 460 microseconds. The most questionable assumption in the models is that the acetylcholine (ACh) is released instantaneously. Modifying the model, so that ACh diffuses from the vesicle through a pore, lengthens the rise time to observed levels. It has been proposed that ACh is released from the vesicle in exchange for Na+. However, the rise times of miniature endplate currents recorded in solutions in which the Na+ is replaced by sucrose are in the normal range. The Q10 for the rise of miniature endplate currents is approximately 2, which is consistent with the models and with temperature effects on pore formation in mast cells.

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Year:  1995        PMID: 7669892      PMCID: PMC1236233          DOI: 10.1016/S0006-3495(95)79884-8

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  40 in total

1.  Effects of permeant monovalent cations on end-plate channels.

Authors:  P W Gage; D Van Helden
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

Review 2.  Generation of end-plate potentials.

Authors:  P W Gage
Journal:  Physiol Rev       Date:  1976-01       Impact factor: 37.312

3.  Quantal independence and uniformity of presynaptic release kinetics at the frog neuromuscular junction.

Authors:  E F Barrett; C F Stevens
Journal:  J Physiol       Date:  1972-12       Impact factor: 5.182

4.  Thick slurry bevelling: a new technique for bevelling extremely fine microelectrodes and micropipettes.

Authors:  W J Lederer; A J Spindler; D A Eisner
Journal:  Pflugers Arch       Date:  1979-09       Impact factor: 3.657

5.  Effects of membrane potential, temperature and neostigmine on the conductance change caused by a quantum or acetylcholine at the toad neuromuscular junction.

Authors:  P W Gage; R N McBurney
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

6.  Acetylcholinesterase density and turnover number at frog neuromuscular junctions, with modeling of their role in synaptic function.

Authors:  L Anglister; J R Stiles; M M Salpeter
Journal:  Neuron       Date:  1994-04       Impact factor: 17.173

7.  An analysis of the action of a false transmitter at the neuromuscular junction.

Authors:  D Colquhoun; W A Large; H P Rang
Journal:  J Physiol       Date:  1977-04       Impact factor: 5.182

8.  End-plate currents and acetylcholine noise at normal and myasthenic human end-plates.

Authors:  S G Cull-Candy; R Miledi; A Trautmann
Journal:  J Physiol       Date:  1979-02       Impact factor: 5.182

9.  The binding of acetylcholine to receptors and its removal from the synaptic cleft.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

10.  Spontaneous and evoked activity of motor nerve endings in calcium Ringer.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

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  12 in total

1.  The temperature sensitivity of miniature endplate currents is mostly governed by channel gating: evidence from optimized recordings and Monte Carlo simulations.

Authors:  J R Stiles; I V Kovyazina; E E Salpeter; M M Salpeter
Journal:  Biophys J       Date:  1999-08       Impact factor: 4.033

2.  Analytical description of the activation of multi-state receptors by continuous neurotransmitter signals at brain synapses.

Authors:  V V Uteshev; P S Pennefather
Journal:  Biophys J       Date:  1997-03       Impact factor: 4.033

3.  Spontaneous and uniquantal-evoked endplate currents in normal frogs are indistinguishable.

Authors:  W Van der Kloot
Journal:  J Physiol       Date:  1996-04-01       Impact factor: 5.182

4.  Miniature endplate current rise times less than 100 microseconds from improved dual recordings can be modeled with passive acetylcholine diffusion from a synaptic vesicle.

Authors:  J R Stiles; D Van Helden; T M Bartol; E E Salpeter; M M Salpeter
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

5.  The effects of geometrical parameters on synaptic transmission: a Monte Carlo simulation study.

Authors:  P J Kruk; H Korn; D S Faber
Journal:  Biophys J       Date:  1997-12       Impact factor: 4.033

6.  A mathematical description of miniature postsynaptic current generation at central nervous system synapses.

Authors:  V V Uteshev; P S Pennefather
Journal:  Biophys J       Date:  1996-09       Impact factor: 4.033

7.  Accounting for the shapes and size distributions of miniature endplate currents.

Authors:  W Van der Kloot; L A Naves
Journal:  Biophys J       Date:  1996-05       Impact factor: 4.033

8.  A mechanism for discharge of charged excitatory neurotransmitter.

Authors:  R Khanin; H Parnas; L Segel
Journal:  Biophys J       Date:  1997-02       Impact factor: 4.033

9.  Control of neurotransmitter release by an internal gel matrix in synaptic vesicles.

Authors:  David Reigada; Ismael Díez-Pérez; Pau Gorostiza; Albert Verdaguer; Inmaculada Gómez de Aranda; Oriol Pineda; Jaume Vilarrasa; Jordi Marsal; Joan Blasi; Jordi Aleu; Carles Solsona
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-10       Impact factor: 11.205

10.  Neurotransmitter discharge and postsynaptic rise times.

Authors:  R Khanin; L Segel; H Parnas; E Ratner
Journal:  Biophys J       Date:  1996-04       Impact factor: 4.033

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