Literature DB >> 11484767

Adult dystrophic (mdx) endplates exhibit reduced quantal size and enhanced quantal variation.

C G Carlson1, D M Roshek.   

Abstract

Examination of miniature endplate potential (MEPP) distributions indicated that the average quantal size is significantly reduced by approximately 44% in young adult mdx mice (5-7 weeks). The average quantum declined further to approximately 37% of non-dystrophic levels in mature (6- to 24-month) mdx mice. Young adult non-dystrophic and mdx endplates and mature non-dystrophic endplates exhibited a linear relationship between the mean and variance of uniquantal MEPP amplitude distributions. Mature mdx endplates, however, exhibited a distinctly nonlinear relationship characterized by large increases in variance at larger mean MEPP amplitudes. These results indicate a reduced average density of functional acetylcholine (ACh) receptors (AChRs) at mdx endplates that, in mature preparations, is associated with greater temporal or spatial variability in the density of functional AChRs apposed to individual release sites.

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Year:  2001        PMID: 11484767     DOI: 10.1007/s004240100561

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  16 in total

1.  Recovery of electrogenesis in skeletal muscles after cell therapy of myodystrophy in MDX mice.

Authors:  V V Kravtsova; V M Mikhailov; A V Sokolova; E V Mikhailova; N A Timonina; E E Nikol'skii; I I Krivoi
Journal:  Dokl Biol Sci       Date:  2012-01-07

2.  The nicotinic acetylcholine receptor and the Na,K-ATPase alpha2 isoform interact to regulate membrane electrogenesis in skeletal muscle.

Authors:  Judith A Heiny; Violetta V Kravtsova; Frederic Mandel; Tatiana L Radzyukevich; Boubacar Benziane; Alexander V Prokofiev; Steen E Pedersen; Alexander V Chibalin; Igor I Krivoi
Journal:  J Biol Chem       Date:  2010-07-01       Impact factor: 5.157

3.  Inspiratory pressure-generating capacity is preserved during ventilatory and non-ventilatory behaviours in young dystrophic mdx mice despite profound diaphragm muscle weakness.

Authors:  David P Burns; Kevin H Murphy; Eric F Lucking; Ken D O'Halloran
Journal:  J Physiol       Date:  2019-01-13       Impact factor: 5.182

Review 4.  Sarcolemmal ion channels in dystrophin-deficient skeletal muscle fibres.

Authors:  Bruno Allard
Journal:  J Muscle Res Cell Motil       Date:  2006-07-28       Impact factor: 2.698

5.  Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubes.

Authors:  Francisco Altamirano; Jose R López; Carlos Henríquez; Tadeusz Molinski; Paul D Allen; Enrique Jaimovich
Journal:  J Biol Chem       Date:  2012-05-01       Impact factor: 5.157

6.  Truncated dystrophins can influence neuromuscular synapse structure.

Authors:  Glen B Banks; Jeffrey S Chamberlain; Stanley C Froehner
Journal:  Mol Cell Neurosci       Date:  2009-01-08       Impact factor: 4.314

7.  Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles.

Authors:  Stephen J P Pratt; Sameer B Shah; Christopher W Ward; Mario P Inacio; Joseph P Stains; Richard M Lovering
Journal:  J Physiol       Date:  2012-10-29       Impact factor: 5.182

8.  Acute failure of action potential conduction in mdx muscle reveals new mechanism of contraction-induced force loss.

Authors:  Jarrod A Call; Gordon L Warren; Mayank Verma; Dawn A Lowe
Journal:  J Physiol       Date:  2013-06-10       Impact factor: 5.182

Review 9.  Alterations of neuromuscular junctions in Duchenne muscular dystrophy.

Authors:  Richard M Lovering; Shama R Iyer; Benjamin Edwards; Kay E Davies
Journal:  Neurosci Lett       Date:  2020-08-17       Impact factor: 3.046

Review 10.  The roles of the dystrophin-associated glycoprotein complex at the synapse.

Authors:  Gonneke S K Pilgram; Saranyapin Potikanond; Richard A Baines; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mol Neurobiol       Date:  2009-11-09       Impact factor: 5.590

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