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Publication : Neuromuscular transmission in dystrophic mice.

First Author  Carbonetto S Year  1977
Journal  J Neurophysiol Volume  40
Issue  4 Pages  836-43
PubMed ID  196056 Mgi Jnum  J:5851
Mgi Id  MGI:54328 Doi  10.1152/jn.1977.40.4.836
Citation  Carbonetto S (1977) Neuromuscular transmission in dystrophic mice. J Neurophysiol 40(4):836-43
abstractText  1. Neuromuscular transmission was studied in the extensor digitorum-longus muscle of dystrophic mice (strain 129/ReJ) by means of intracellular recording techniques. 2. In a large population of normal and dystrophic muscle fibers tested, the incidence of transmission failure was about 2% and showed no significant difference between the two groups. 3. Quantal size and quantum content of dystrophic junctions were found to be normal. This was true even of nerve terminal on apparently atrophied muscle fibers. 4. The facilitation ratio at dystrophic junctions was not significantly different from normal. 5. Dystrophic neuromuscular junctions exhibited an abnormality high frequency of giant spontaneous potentials. Application of tetrodotoxin (10(-6) M) and curare (10(-6) M) indicated that these potentials were caused by impulse-independent release of acetylcholine. 6. Neuromuscular transmission in dystrophic mice was found functionally normal and unrelated to the degenerative state of the muscle.
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