Literature DB >> 925722

Suppression by elevated calcium of black widow spider venom activity at frog neuromuscular junctions.

J E Smith, A W Clark, T A Kuster.   

Abstract

Frog neuromuscular junctions were treated with both concentrated black widow spider venom (BWSV) and elevated extracellular calcium (5-50 mM). This procedure causes a dramatic increase in the frequency of spontaneous miniature endplate potentials (mepps) which persists for only a few minutes. In contrast, BWSV-induced mepp activity, the venom effect (VE), continues for 20 min-1 h at junctions in elevated calcium Ringer solutions treated with doses of dilute venom or at junctions in normal calcium (1.91 mM) Ringer solution treated with concentrated venom. Following the disappearance of the VE in elevated extracellular calcium, only a few normal amplitude mepps and a few giant amplitude mepps are observed. The disappearance of the VE in these preparations is irreversible and occurs whether exposure to elevated extracellular calcium precedes or follows exposure to BWSV. Electron microscopy indicates that the major structural alterations produced by exposure to concentrated BWSV and 20 mM calcium Ringer solution are the swelling of nerve terminal mitochondria and the clumping of synaptic vesicles, large numbers of which remain in the terminals. Exposure to 20 mM calcium Ringer solution alone produces no ultrastructural modifications in these preparations. These observations can best be explained if one of the effects of BWSV is to increase the permeability of the nerve terminal membrane to calcium. Only doses of concentrated venom can sufficiently elevate intracellular calcium to a concentration at which synaptic vesicles clump together, thus interruping the transmitter release process.

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Year:  1977        PMID: 925722     DOI: 10.1007/bf01205217

Source DB:  PubMed          Journal:  J Neurocytol        ISSN: 0300-4864


  10 in total

Review 1.  Structure, Distribution, and Function of Neuronal/Synaptic Spinules and Related Invaginating Projections.

Authors:  Ronald S Petralia; Ya-Xian Wang; Mark P Mattson; Pamela J Yao
Journal:  Neuromolecular Med       Date:  2015-05-26       Impact factor: 3.843

2.  Neurotransmitter release and nerve terminal morphology at the frog neuromuscular junction affected by the dye Erythrosin B.

Authors:  G J Augustine; H Levitan
Journal:  J Physiol       Date:  1983-01       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.  Effect of alpha-latrotoxin on the frog neuromuscular junction at low temperature.

Authors:  B Ceccarelli; W P Hurlbut; N Iezzi
Journal:  J Physiol       Date:  1988-08       Impact factor: 5.182

5.  Action of black widow spider venom on quantized release of acetylcholine at the frog neuromuscular junction: dependence upon external Mg2+.

Authors:  S Misler; W P Hurlbut
Journal:  Proc Natl Acad Sci U S A       Date:  1979-02       Impact factor: 11.205

6.  Release of neurotransmitters and depletion of synaptic vesicles in cerebral cortex slices by alpha-latrotoxin from black widow spider venom.

Authors:  M C Tzeng; R S Cohen; P Siekevitz
Journal:  Proc Natl Acad Sci U S A       Date:  1978-08       Impact factor: 11.205

7.  Structural evidence that botulinum toxin blocks neuromuscular transmission by impairing the calcium influx that normally accompanies nerve depolarization.

Authors:  N Hirokawa; J E Heuser
Journal:  J Cell Biol       Date:  1981-01       Impact factor: 10.539

8.  Ca2+-dependent recycling of synaptic vesicles at the frog neuromuscular junction.

Authors:  B Ceccarelli; W P Hurlbut
Journal:  J Cell Biol       Date:  1980-10       Impact factor: 10.539

9.  Alpha-latrotoxin channels in neuroblastoma cells.

Authors:  W P Hurlbut; E Chieregatti; F Valtorta; C Haimann
Journal:  J Membr Biol       Date:  1994-02       Impact factor: 1.843

10.  Reversibility and mode of action of Black Widow spider venom on the vertebrate neuromuscular junction.

Authors:  A Gorio; A Mauro
Journal:  J Gen Physiol       Date:  1979-02       Impact factor: 4.086

  10 in total

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