» Articles » PMID: 240928

Binomial Analysis of Quantal Transmitter Release at Glycerol Treated Frog Neuromuscular Junctions

Overview
Journal J Physiol
Specialty Physiology
Date 1975 Aug 1
PMID 240928
Citations 53
Authors
Affiliations
Soon will be listed here.
Abstract

1. Transmitter release was analysed at frog neuromuscular junctions pre-treated with 400 mM glycerol Ringer. In the absence of added drugs, end-plate potentials (e.p.p.s) and miniature e.p.p.s (m.e.p.p.s) could be recorded at selected junctions. 2. E.p.p.s were unusually large and calculations of quantal content indicated a high level of release. Also recorded were anomalous action potentials resembling e.p.p.s but these could be distinguished using a summation test. 3. Plots of coefficient of variation of e.p.p.s (0-5 Hz stimulation) versus direct quantal content (M1) showed a marked deviation from Poisson expectations with high M1. Analysis of these results with amplitude-frequency histograms showed a progressively better fit to binomial predictions with increasing M1. 4. The use of binomial statistics allowed direct calculations of the mean probability of release (p) and the readily available store (n). Increasing Ca/Mg caused increases in both n and p. 5. Plots of M1 vs. Ca/Mg showed a power relationship of 3.58. Maximum m.e.p.p. amplitude occurred at control Ca/Mg. Both results were consistent with studies in muscles not treated with glycerol and indicated that glycerol treatment caused no major alterations pre- or post-junctionally. 6. Estimates of quantum size using Poisson assumptions showed an over-all increase when stimulus frequency was raised, indicating a shift from binomial to a Poisson distribution. 7. The combined findings demonstrate that the glycerol treated preparation can be used to examine the release process during high output. Such release conforms to binomial statistics and allows direct determinations of the parameters n and p.

Citing Articles

Exact Distribution of the Quantal Content in Synaptic Transmission.

Rijal K, Muller N, Friauf E, Singh A, Prasad A, Das D Phys Rev Lett. 2024; 132(22):228401.

PMID: 38877921 PMC: 11571698. DOI: 10.1103/PhysRevLett.132.228401.


Homeostatic Plasticity of the Mammalian Neuromuscular Junction.

Engisch K, Wang X, Rich M Adv Neurobiol. 2022; 28:111-130.

PMID: 36066823 DOI: 10.1007/978-3-031-07167-6_5.


Homeostatic synaptic plasticity at the neuromuscular junction in myasthenia gravis.

Wang X, Rich M Ann N Y Acad Sci. 2017; 1412(1):170-177.

PMID: 28981978 PMC: 5790634. DOI: 10.1111/nyas.13472.


Synaptic Connectivity between Renshaw Cells and Motoneurons in the Recurrent Inhibitory Circuit of the Spinal Cord.

Moore N, Bhumbra G, Foster J, Beato M J Neurosci. 2015; 35(40):13673-86.

PMID: 26446220 PMC: 4595620. DOI: 10.1523/JNEUROSCI.2541-15.2015.


Different neuropeptides are expressed in different functional subsets of cholinergic excitatory motorneurons in the nematode Ascaris suum.

Konop C, Knickelbine J, Sygulla M, Vestling M, Stretton A ACS Chem Neurosci. 2015; 6(6):855-70.

PMID: 25812635 PMC: 4769031. DOI: 10.1021/cn5003623.


References
1.
Martin A . A further study of the statistical composition on the end-plate potential. J Physiol. 1955; 130(1):114-22. PMC: 1363457. DOI: 10.1113/jphysiol.1955.sp005397. View

2.
Maeno T, Edwards C . Neuromuscular facilitation with low-frequency stimulation and effects of some drugs. J Neurophysiol. 1969; 32(5):785-92. DOI: 10.1152/jn.1969.32.5.785. View

3.
Del Castillo J, Katz B . Quantal components of the end-plate potential. J Physiol. 1954; 124(3):560-73. PMC: 1366292. DOI: 10.1113/jphysiol.1954.sp005129. View

4.
Del Castillo J, Katz B . The effect of magnesium on the activity of motor nerve endings. J Physiol. 1954; 124(3):553-9. PMC: 1366291. DOI: 10.1113/jphysiol.1954.sp005128. View

5.
Del Castillo J, ENGBAEK L . The nature of the neuromuscular block produced by magnesium. J Physiol. 1954; 124(2):370-84. PMC: 1366273. DOI: 10.1113/jphysiol.1954.sp005114. View