The effects of nerve terminal activity on non-quantal release of acetylcholine at the mouse neuromuscular junction
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
PubMed
2388160
PubMed Central
PMC1189779
DOI
10.1113/jphysiol.1990.sp018044
Knihovny.cz E-zdroje
- MeSH
- acetylcholin metabolismus MeSH
- atropin farmakologie MeSH
- cholinesterasové inhibitory farmakologie MeSH
- elektrická stimulace MeSH
- myši MeSH
- nervosvalová ploténka fyziologie MeSH
- nervosvalové spojení účinky léků metabolismus fyziologie MeSH
- nervová zakončení účinky léků metabolismus fyziologie MeSH
- ouabain farmakologie MeSH
- oxotremorin farmakologie MeSH
- techniky in vitro MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- acetylcholin MeSH
- atropin MeSH
- cholinesterasové inhibitory MeSH
- ouabain MeSH
- oxotremorin MeSH
1. Local endplate depolarization induced by anticholinesterase application to mouse nerve-diaphragm preparations was taken as a measure of non-quantal release of acetylcholine. 2. Non-quantal acetylcholine release occurred within 20-60 s after anticholinesterase application, either spontaneously or evoked by nerve stimulation. Non-quantal release declined with time and disappeared after 3-5 min. 3. The amplitude of stimulation-evoked non-quantal release increased with the frequency of stimulation and was maximal at frequencies above 50 Hz. Two stimuli were sufficient to evoke the maximal effect. 4. Micromolar concentrations of atropine, pirenzepine and vesamicol reduced the amplitude and shortened the duration of non-quantal release. Oxotremorine (10(-8) M) enhanced the amplitude and ouabain (10(-4) M) prolonged the duration of non-quantal release. 5. Our results support the idea that the non-quantal release is due to the vesicular acetylcholine transport system which becomes transiently a part of the nerve terminal during exocytotic release of quantal acetylcholine.
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