Literature DB >> 16758584

Causes of the increased fiber density in muscular dystrophies studied with single fiber EMG during electrical stimulation.

P Hilton-Brown1, E Stålberg, J Trontelj, M Mihelin.   

Abstract

The impulse transmission in motor end-plates and along muscle fibers was studied with single fiber EMG in 13 patients with muscular dystrophy during intramuscular nerve stimulation and direct muscle fiber stimulation. For comparison, three patients with spinal muscular atrophy (SMA) and five normal subjects were studied. At nerve stimulation, 25% of the recordings in the patients with muscular dystrophy showed "increased" jitter (> 55 microsec), 48% "normal" (10-55 microsec), and 27% "abnormally low" jitter (< 5 microsec). At direct muscle fiber stimulation, the jitter was "abnormally low" in 91% of the recordings; 9% of the recordings had normal jitter. In SMA, no abnormally low jitter values were found. Increased jitter is a sign of impaired impulse transmission in immature intramuscular nerves and motor end-plates. "Abnormally low jitter" suggests the presence of branched muscle fibers and ephaptic transmission between hyperexcitable fibers.

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Year:  1985        PMID: 16758584     DOI: 10.1002/mus.880080507

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  5 in total

1.  A muscle architecture model offering control over motor unit fiber density distributions.

Authors:  Javier Navallas; Armando Malanda; Luis Gila; Javier Rodríguez; Ignacio Rodríguez
Journal:  Med Biol Eng Comput       Date:  2010-06-10       Impact factor: 2.602

2.  Jitter in the muscle fibre.

Authors:  J V Trontelj; E Stålberg; M Mihelin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-01       Impact factor: 10.154

3.  Axonal stimulation for end-plate jitter studies.

Authors:  J V Trontelj; M Mihelin; J M Fernandez; E Stålberg
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-06       Impact factor: 10.154

Review 4.  Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.

Authors:  Joe N Kornegay; Janet R Bogan; Daniel J Bogan; Martin K Childers; Juan Li; Peter Nghiem; David A Detwiler; C Aaron Larsen; Robert W Grange; Ratna K Bhavaraju-Sanka; Sandra Tou; Bruce P Keene; James F Howard; Jiahui Wang; Zheng Fan; Scott J Schatzberg; Martin A Styner; Kevin M Flanigan; Xiao Xiao; Eric P Hoffman
Journal:  Mamm Genome       Date:  2012-01-05       Impact factor: 2.957

5.  Cycles of myofiber degeneration and regeneration lead to remodeling of the neuromuscular junction in two mammalian models of Duchenne muscular dystrophy.

Authors:  Seth G Haddix; Young Il Lee; Joe N Kornegay; Wesley J Thompson
Journal:  PLoS One       Date:  2018-10-31       Impact factor: 3.240

  5 in total

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