Literature DB >> 6308500

A new type of transmitter release at the neuromuscular junction.

S Thesleff, J Molgó.   

Abstract

Examination of spontaneous miniature endplate potentials (MEPPs) in murine skeletal muscle has revealed that in conditions such as botulinum poisoning, during nerve terminal regeneration or in the presence of the drug 4-aminoquinoline, two types of acetylcholine release are responsible for the MEPPs. In addition to the MEPPs which correspond to the quantal component of a nerve impulse-evoked endplate potential a second type of acetylcholine release occurs. The latter type of transmitter release gives rise to MEPPs with a more prolonged time-to-peak and frequently a larger than normal amplitude. It is unaffected by nerve terminal depolarization and transmembrane Ca2+ fluxes. The relationship between MEPP frequency and temperature has a Q10 of about 12 compared to 2-3 for normal MEPPs. In botulinum-poisoned muscles this secretory type of transmitter release dominates, being exclusively present in muscles where nerve stimulation fails to release transmitter. In normal muscle such a release is induced by 4-aminoquinoline which may cause up to 45% of all the spontaneous MEPPs to be of that kind. It is suggested that the described spontaneous secretion of acetylcholine serves in inductory and neurotrophic function.

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Year:  1983        PMID: 6308500     DOI: 10.1016/0306-4522(83)90041-6

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  12 in total

1.  Caffeine- and ryanodine-induced changes in the spectrum of spontaneously secreted quanta of the mediator in the neuromuscular synapse of mice.

Authors:  O P Balezina; N V Surova; V I Lapteva
Journal:  Dokl Biol Sci       Date:  2001 Sep-Oct

Review 2.  Application of the theory of homeoviscous adaptation to excitable membranes: pre-synaptic processes.

Authors:  A G Macdonald
Journal:  Biochem J       Date:  1988-12-01       Impact factor: 3.857

3.  A comparison of miniature end-plate potentials at normal, denervated, and long-term botulinum toxin type A poisoned frog neuromuscular junctions.

Authors:  M T Lupa; S P Yu
Journal:  Pflugers Arch       Date:  1986-11       Impact factor: 3.657

4.  The effects of in vitro application of purified botulinum neurotoxin at mouse motor nerve terminals.

Authors:  J O Dolly; S Lande; D W Wray
Journal:  J Physiol       Date:  1987-05       Impact factor: 5.182

Review 5.  Physiology and pharmacology of neuromuscular transmission, with special reference to the possible consequences of prolonged blockade.

Authors:  W C Bowman
Journal:  Intensive Care Med       Date:  1993       Impact factor: 17.440

6.  Modulation of Ca(2+)-dependent and Ca(2+)-independent miniature endplate potentials by phorbol ester and adenosine in frog.

Authors:  Timothy J Searl; Eugene M Silinsky
Journal:  Br J Pharmacol       Date:  2005-08       Impact factor: 8.739

7.  Acetylcholine release at identified nerve terminals in the organ-cultured frog neuromuscular preparation.

Authors:  R Cherki-Vakil; H Meiri
Journal:  J Physiol       Date:  1990-04       Impact factor: 5.182

8.  The nature and origin of calcium-insensitive miniature end-plate potentials at rodent neuromuscular junctions.

Authors:  M T Lupa; N Tabti; S Thesleff; F Vyskocil; S P Yu
Journal:  J Physiol       Date:  1986-12       Impact factor: 5.182

9.  The timing of channel opening during miniature endplate currents at the frog and mouse neuromuscular junctions: effects of fasciculin-2, other anti-cholinesterases and vesamicol.

Authors:  W Van der Kloot; O P Balezina; J Molgó; L A Naves
Journal:  Pflugers Arch       Date:  1994-09       Impact factor: 3.657

10.  On the possible origin of giant or slow-rising miniature end-plate potentials at the neuromuscular junction.

Authors:  L C Sellin; J Molgó; K Törnquist; B Hansson; S Thesleff
Journal:  Pflugers Arch       Date:  1996-01       Impact factor: 3.657

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