Literature DB >> 1841963

Increasing quantal size at the mouse neuromuscular junction and the role of choline.

S P Yu1, W Van der Kloot.   

Abstract

1. In frog a variety of treatments have been shown to increase quantal size at the neuromuscular junction (NMJ), apparently by releasing more acetylcholine (ACh) per quantum. The present experiments were undertaken to see whether similar changes occur at the mouse NMJ. 2. None of the hormones tested, adrenaline, insulin or corticosteroids, significantly increased quantal size at the mouse NMJ. 3. Soaking diaphragms in hypertonic solution (about 475 mosmol/kg) for 15-30 min roughly doubled the size of miniature endplate potentials (MEPPs), miniature endplate currents (MEPCs), and uniquantal endplate potentials (EPPs). We will refer to these as 'large quanta'. Note that all of the measurements were made after returning the preparation to normal (Tyrode) solution. 4. In frog hypertonic solution made with sodium gluconate replacing NaCl increases quantal size four- rather than two-fold. In mouse there was little difference in the effects of solutions made with the two anions. In Cl(-)-free hypertonic solution, made with sodium gluconate and SO4(2-) solutions, quantal size increase is somewhat less, so there may be a role for Cl- in enlarging quantal size. 5. After hypertonic treatment, quantal size remained elevated for at least 1 h and then gradually declined back to usual levels. The data suggest a gradual decrease in mean quantal size, rather than the appearance of a new subpopulation of smaller quanta. 6. Hypertonic treatment did not change the endplate depolarization in response to ionophoretically applied ACh. This suggests that the increased quantal size is not due to a postsynaptic change. Large MEPP's disappear in the presence of tubocurarine and reappear when the drug is washed away. 7. Vesamicol is an inhibitor of active ACh uptake into isolated synaptic vesicles. 5 microM-vesamicol has no detectable postjunctional effect. However, when vesamicol was included in the Tyrode and the hypertonic solutions the increase in quantal size was blocked. This is further evidence that the large quanta are produced by the release of more ACh per quantum. 8. Even when added after the hypertonic treatment, vesamicol soon decreased quantal size back to the normal level. Two other inhibitors of active ACh uptake into vesicles, tetraphenylboron (TPB) and hexanitrodiphenylamine (HNPA) also decreased quantal size after hypertonic treatment, apparently by a presynaptic action. This suggests that the additional ACh that produces large miniatures may be incorporated into the quanta shortly before release.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1841963      PMCID: PMC1181395          DOI: 10.1113/jphysiol.1991.sp018450

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  37 in total

1.  Statistical and graphical methods for testing the hypothesis that quanta are made up of subunits.

Authors:  W Van der Kloot
Journal:  J Neurosci Methods       Date:  1989-02       Impact factor: 2.390

2.  Variability of transmitter quanta released during incorporation of a false transmitter into cholinergic nerve terminals.

Authors:  W A Large; H P Rang
Journal:  J Physiol       Date:  1978-12       Impact factor: 5.182

3.  Factors affecting the rate of incorporation of a false transmitter into mammalian motor nerve terminals.

Authors:  W A Large; H P Rang
Journal:  J Physiol       Date:  1978-12       Impact factor: 5.182

4.  An examination of the effects of osmotic pressure changes upon transmitter release from mammalian motor nerve terminals.

Authors:  J I Hubbard; S F Jones; E M Landau
Journal:  J Physiol       Date:  1968-08       Impact factor: 5.182

5.  Effect of aconitine on the sodium permeability of the node of Ranvier.

Authors:  H Schmidt; O Schmitt
Journal:  Pflugers Arch       Date:  1974-06-11       Impact factor: 3.657

6.  The timing of channel opening during miniature end-plate currents.

Authors:  I Cohen; W van der Kloot; D Attwell
Journal:  Brain Res       Date:  1981-10-26       Impact factor: 3.252

7.  Effects of nerve activity on the postsynaptic membrane of skeletal muscle.

Authors:  G Vrbová; A C Wareham
Journal:  Brain Res       Date:  1976-12-24       Impact factor: 3.252

8.  The effect of prednisolone on neuromuscular transmission in the rat diaphragm.

Authors:  H Van Wilgenburg
Journal:  Eur J Pharmacol       Date:  1979-05-15       Impact factor: 4.432

9.  An analysis of the action of a false transmitter at the neuromuscular junction.

Authors:  D Colquhoun; W A Large; H P Rang
Journal:  J Physiol       Date:  1977-04       Impact factor: 5.182

10.  Inhibition of [3H]acetylcholine active transport by tetraphenylborate and other anions.

Authors:  D C Anderson; S C King; S M Parsons
Journal:  Mol Pharmacol       Date:  1983-07       Impact factor: 4.436

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  10 in total

1.  Spontaneous and uniquantal-evoked endplate currents in normal frogs are indistinguishable.

Authors:  W Van der Kloot
Journal:  J Physiol       Date:  1996-04-01       Impact factor: 5.182

2.  Accounting for the shapes and size distributions of miniature endplate currents.

Authors:  W Van der Kloot; L A Naves
Journal:  Biophys J       Date:  1996-05       Impact factor: 4.033

3.  Acetylcholine receptors in the equatorial region of intrafusal muscle fibres modulate mouse muscle spindle sensitivity.

Authors:  Laura Gerwin; Corinna Haupt; Katherine A Wilkinson; Stephan Kröger
Journal:  J Physiol       Date:  2019-02-13       Impact factor: 5.182

4.  Repetitive nerve stimulation decreases the acetylcholine content of quanta at the frog neuromuscular junction.

Authors:  L A Naves; W Van der Kloot
Journal:  J Physiol       Date:  2001-05-01       Impact factor: 5.182

5.  Bromoacetylcholine and acetylcholinesterase introduced via liposomes into motor nerve endings block increases in quantal size.

Authors:  E Brailoiu; W V der Kloot
Journal:  Pflugers Arch       Date:  1996-07       Impact factor: 3.657

6.  Role of acetylcholinesterase on the structure and function of cholinergic synapses: insights gained from studies on knockout mice.

Authors:  Michael Adler; Richard E Sweeney; Tracey A Hamilton; Oksana Lockridge; Ellen G Duysen; Angela L Purcell; Sharad S Deshpande
Journal:  Cell Mol Neurobiol       Date:  2011-05-03       Impact factor: 5.046

7.  Motor neuron-specific overexpression of the presynaptic choline transporter: impact on motor endurance and evoked muscle activity.

Authors:  D Lund; A M Ruggiero; S M Ferguson; J Wright; B A English; P A Reisz; S M Whitaker; A C Peltier; R D Blakely
Journal:  Neuroscience       Date:  2010-10-01       Impact factor: 3.590

8.  Effects of activators and inhibitors of protein kinase A on increases in quantal size at the frog neuromuscular junction.

Authors:  W Van der Kloot; D D Brănişteanu
Journal:  Pflugers Arch       Date:  1992-03       Impact factor: 3.657

9.  Nicotinic agonists antagonize quantal size increases and evoked release at frog neuromuscular junction.

Authors:  W Van der Kloot
Journal:  J Physiol       Date:  1993-08       Impact factor: 5.182

10.  Excitatory-inhibitory imbalance in hypoglossal neurons during the critical period of postnatal development in the rat.

Authors:  Xiu-ping Gao; Qing-song Liu; Qiuli Liu; Margaret T T Wong-Riley
Journal:  J Physiol       Date:  2011-02-28       Impact factor: 6.228

  10 in total

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