Literature DB >> 21913115

Electrophysiological characterization of neuromuscular synaptic dysfunction in mice.

Yoshie Sugiura1, Fujun Chen, Yun Liu, Weichun Lin.   

Abstract

Emerging evidence suggests that synaptic dysfunction occurs prior to neuronal loss in neurodegenerative diseases, such as amyotrophic lateral sclerosis (ALS). Therefore, monitoring synaptic activity during early stages of neurodegeneration may provide valuable information for the development of diagnostic and/or therapeutic strategies. Here, we describe an electrophysiological method routinely applied in our laboratory for investigating synaptic activity of the neuromuscular junction (NMJ), the synaptic connection between motoneurons and skeletal muscles. Using conventional intracellular sharp electrodes, both spontaneous synaptic activity (miniature end-plate potentials) and evoked synaptic activity (end-plate potentials) can be readily recorded in acutely isolated nerve-muscle preparations. This method can also be adapted to various simulation protocols for studying short-term plasticity of neuromuscular synapses.

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Year:  2011        PMID: 21913115      PMCID: PMC4590777          DOI: 10.1007/978-1-61779-328-8_26

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  29 in total

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4.  Blocking skeletal muscle DHPRs/Ryr1 prevents neuromuscular synapse loss in mutant mice deficient in type III Neuregulin 1 (CRD-Nrg1).

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