Literature DB >> 6969296

Sprouting and regression of the nerve at the frog neuromuscular junction in normal conditions and after prolonged paralysis with curare.

A Wernig, M Pécot-Dechavassine, H Stover.   

Abstract

A light microscopical, histochemical and electron microscopical investigation of the frog neuromuscular junction has been performed on muscles from animals in different functional states of activity. The combined staining of axon terminals and cholinesterase (ChE) allows a precise description of the nerve terminal arborization and its synaptic contacts. Most terminal arborizations form long continuous contacts with the muscle cell. Distinquishable from these are nerve branches (usually of small diameter)d or distal endings of branches with one or several small and isolated contacts. It is assumed that these are sprouts with newly-formed synaptic sites. Other sprouts end without apparent synaptic contact. At the uttrastructural levet, nerve sprouts end without apparent synaptic contact. At the uttrastructural levet, nerve sprouts growing into empty, well-differentiated synaptic gutters or inducing the formation of new synaptic sites were observed. In other sites, ChE is apparently located at postsynaptic gutters with no nerve present. Similarly, in the electron microscope, well-differentiated synaptic gutters lacking any nerve or Schwann cell elements were observed. In addition, synaptic gutters only partially occupied by the nerve were frequently seen. These features have been interpreted as signs of regression of the nerve terminals. Nerve regression and sprouting were found in animals chronically paralysed with curare over several weeks as well as in untreated frogs (winter and summer frogs, laboratory frogs, fed and unfed). When quantitatively evaluating the occurence of presumed features of nerve sprouting and nerve regression, differences were found between different experimental groups. From this it is concluded that, in addition to developmental changes, the degree of nerve sprouting and regression is controlled by external factors such as muscle activity and seasonal variations. Signs of sprouting and nerve regression can be simultaneously present in a single synapse. It appears that the frog neuromuscular synapse is not a static structure, but is in a state of permenent remodelling.

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Year:  1980        PMID: 6969296     DOI: 10.1007/BF01181538

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


  27 in total

1.  Formation and function of synapses with respect to Schwann cells at the end of motor nerve terminal branches on mature amphibian (Bufo marinus) muscle.

Authors:  G T Macleod; P A Dickens; M R Bennett
Journal:  J Neurosci       Date:  2001-04-01       Impact factor: 6.167

Review 2.  Aging and muscle function.

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Review 3.  Perisynaptic Schwann Cells at the Neuromuscular Synapse: Adaptable, Multitasking Glial Cells.

Authors:  Chien-Ping Ko; Richard Robitaille
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-08-20       Impact factor: 10.005

4.  Stathmin is required for stability of the Drosophila neuromuscular junction.

Authors:  Ethan R Graf; Heather M Heerssen; Christina M Wright; Graeme W Davis; Aaron DiAntonio
Journal:  J Neurosci       Date:  2011-10-19       Impact factor: 6.167

5.  Prolonged nerve stimulation causes changes in transmitter release at the frog neuromuscular junction.

Authors:  I Hinz; A Wernig
Journal:  J Physiol       Date:  1988-07       Impact factor: 5.182

6.  In vivo long-term synaptic plasticity of glial cells.

Authors:  Eve-Lyne Bélair; Joanne Vallée; Richard Robitaille
Journal:  J Physiol       Date:  2010-02-08       Impact factor: 5.182

7.  Nerve terminal growth remodels neuromuscular synapses in mice following regeneration of the postsynaptic muscle fiber.

Authors:  Yue Li; Wesley J Thompson
Journal:  J Neurosci       Date:  2011-09-14       Impact factor: 6.167

8.  Precision of reinnervation and synaptic remodeling observed in neuromuscular junctions of living frogs.

Authors:  S H Astrow; V Pitaevski; A A Herrera
Journal:  J Neurosci       Date:  1996-08-15       Impact factor: 6.167

9.  Changes in motor nerve terminals during bupivacaine-induced postsynaptic deprivation.

Authors:  J Tomas i Ferré; R Fenoll i Brunet; M Santafé; E Mayayo
Journal:  J Anat       Date:  1989-02       Impact factor: 2.610

Review 10.  Physiological adaptations to resistance exercise. Implications for athletic conditioning.

Authors:  W J Kraemer; M R Deschenes; S J Fleck
Journal:  Sports Med       Date:  1988-10       Impact factor: 11.136

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