Literature DB >> 6835395

Synapse elimination in neonatal rat muscle is sensitive to pattern of muscle use.

W Thompson.   

Abstract

The synaptic connections among the cells of the vertebrate nervous system undergo extensive rearrangements early in development. During their initial growth, neurones apparently form synaptic connections with an excessive number of targets, later retracting a portion of these synapses in establishing the adult neural circuits. Because of the profound effects which experience has upon the developing nervous system, a question of considerable interest has been the role which the functional use of these developing synapses might play in determining the final pattern of connectivity. At the neuromuscular junction the early changes in synaptic connections are well documented, and here questions about the importance of function can be relatively easily addressed. Mammalian skeletal muscle fibres experience a perinatal period of synapse elimination so that all but one of several synapses formed on each muscle fibre are lost. This synapse elimination is sensitive to alterations of neuromuscular use or activity. Reduction of muscle use by tenotomy or by paralysis of the muscle with drugs blocking nerve impulse conduction or neuromuscular transmission delays or even prevents synapse loss, while increased use produced by stimulation of the muscle nerve apparently accelerates the rate at which synapses are lost. I report here a further examination of the role of neuromuscular activity in synapse elimination. I show that chronic neuromuscular stimulation accelerates synapse elimination but that this acceleration is dependent on the temporal pattern in which the stimuli are presented: brief stimulus trains containing 100 Hz bursts of stimuli produce this acceleration whereas the same number of stimuli presented continuously at 1 Hz do not. Furthermore, the 100 Hz activity pattern which is effective in altering synapse elimination also alters two other muscle properties: the sensitivity of the muscle fibers to acetylcholine and the 'speed' of muscle contractions. These findings suggest that the ability of muscle fibres to maintain more than one nerve terminal, like other muscle properties, is sensitive to the pattern of muscle use rather than just the total amount of use.

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Year:  1983        PMID: 6835395     DOI: 10.1038/302614a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  31 in total

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Journal:  J Neurosci       Date:  2001-07-15       Impact factor: 6.167

2.  The role of synaptobrevin1/VAMP1 in Ca2+-triggered neurotransmitter release at the mouse neuromuscular junction.

Authors:  Yun Liu; Yoshie Sugiura; Weichun Lin
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3.  Spike timing plays a key role in synapse elimination at the neuromuscular junction.

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Review 4.  Roles for neuronal and glial autophagy in synaptic pruning during development.

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Review 5.  Developmental neuromuscular synapse elimination: Activity-dependence and potential downstream effector mechanisms.

Authors:  Young Il Lee
Journal:  Neurosci Lett       Date:  2019-12-23       Impact factor: 3.046

6.  Development of the sympathetic innervation to the cerebral arterial system in neonatal rats as revealed by anterograde labeling with wheatgerm agglutinin-horseradish peroxidase.

Authors:  Y Handa; Y Nojyo; N Tamamaki; A Tsuchida; T Kubota
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7.  Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons.

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8.  Neuregulin1 displayed on motor axons regulates terminal Schwann cell-mediated synapse elimination at developing neuromuscular junctions.

Authors:  Young Il Lee; Yue Li; Michelle Mikesh; Ian Smith; Klaus-Armin Nave; Markus H Schwab; Wesley J Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2016-01-11       Impact factor: 11.205

9.  Relationship of insulin-like growth factor II gene expression in muscle to synaptogenesis.

Authors:  D N Ishii
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

10.  Activation patterns of embryonic chick hind-limb muscles following blockade of activity and motoneurone cell death.

Authors:  L T Landmesser; M Szente
Journal:  J Physiol       Date:  1986-11       Impact factor: 5.182

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