Literature DB >> 2860241

Profiles of evoked release along the length of frog motor nerve terminals.

A J D'Alonzo, A D Grinnell.   

Abstract

In order to determine the relative probability of evoked transmitter release from different parts of frog motor nerve terminals, a technique has been developed in which single quantum end-plate potentials (e.p.p.s) are recorded by two intracellular electrodes, located at opposite ends of identified junctions. The log of the ratio of the amplitudes recorded simultaneously at the two electrodes is a linear function of the distance of the site of origin of the event from each of the two electrodes. Using online computer data acquisition and analysis, and current pulses at known locations for spatial calibration, it is possible to localize the site of single quantum e.p.p.s to within +/- 10-20 micron. Using the frog cutaneous pectoris neuromuscular preparation and a low calcium, high magnesium Ringer solution to ensure mostly single quantum events and failures, several thousand responses were recorded from each junction, allowing construction of a profile of the numbers of single quantum events arising from each portion of the junction. By comparison of junctional morphology and release profiles, it is possible to construct a probability of release per unit length profile for the entire junction. This technique has several advantages over localization of release events by measurements of extracellular synaptic currents. It was found that, for most junctions, the central 60-90% of the terminal exhibited relatively uniform probability of release, with highest levels typically near the point where the axon first contacted the muscle fibre, or in regions with many short terminal branches. However, no instances have been found in which a small region of terminal (10% or less) showed extraordinarily high release levels (30-50% of the total release from the junction). Characteristically, but not invariably, there is reduced release near the ends of terminal branches, especially the longer branches, where release per unit length could be as little as 5-10% of that in proximal portions. Some junctions had large regions of terminal that released very little transmitter. These also showed multiple myelineated axonal inputs, and may have been polyneuronally innervated junctions in which one of the inputs was much weaker than the other.

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Year:  1985        PMID: 2860241      PMCID: PMC1193373          DOI: 10.1113/jphysiol.1985.sp015583

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


  36 in total

1.  The formation of synapses in amphibian striated muscle during development.

Authors:  M R Bennett; A G Pettigrew
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

2.  Localization of active spots within the neuromuscular junction of the frog.

Authors:  J DEL CASTILLO; B KATZ
Journal:  J Physiol       Date:  1956-06-28       Impact factor: 5.182

3.  Structure and ultrastructure of the frog motor endplate. A freeze-etching study.

Authors:  K Peper; F Dreyer; C Sandri; K Akert; H Moor
Journal:  Cell Tissue Res       Date:  1974-06-24       Impact factor: 5.249

4.  Correlation between nerve terminal size and transmitter release at the neuromuscular junction of the frog.

Authors:  M Kuno; S A Turkanis; J N Weakly
Journal:  J Physiol       Date:  1971-03       Impact factor: 5.182

5.  Quantal independence and uniformity of presynaptic release kinetics at the frog neuromuscular junction.

Authors:  E F Barrett; C F Stevens
Journal:  J Physiol       Date:  1972-12       Impact factor: 5.182

6.  Potential changes recorded from the frog motor nerve terminal during its activation.

Authors:  M Braun; R F Schmidt
Journal:  Pflugers Arch Gesamte Physiol Menschen Tiere       Date:  1966

7.  [Synaptic vesicles and pouches at the level of "active zones" of the neuromuscular junction].

Authors:  R Couteaux; M Pécot-Dechavassine
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1970-12-21

8.  The effect of local blockage of motor nerve terminals.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1968-12       Impact factor: 5.182

9.  The binding of acetylcholine to receptors and its removal from the synaptic cleft.

Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

10.  Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction.

Authors:  J E Heuser; T S Reese
Journal:  J Cell Biol       Date:  1973-05       Impact factor: 10.539

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  24 in total

1.  Quantal potential fields around individual active zones of amphibian motor-nerve terminals.

Authors:  M R Bennett; L Farnell; W G Gibson; G T Macleod; P Dickens
Journal:  Biophys J       Date:  2000-03       Impact factor: 4.033

2.  Protein kinase A cascade regulates quantal release dispersion at frog muscle endplate.

Authors:  Ella A Bukharaeva; Dmitry Samigullin; Eugeny Nikolsky; Frantisek Vyskocil
Journal:  J Physiol       Date:  2002-02-01       Impact factor: 5.182

3.  Characteristics of the time course of evoked secretion of transmitter quanta in different parts of the motor nerve ending in the frog.

Authors:  E E Nikol'kii; E A Bukharaeva; D V Samigullin; R Kh Gainulo
Journal:  Neurosci Behav Physiol       Date:  2002 May-Jun

4.  Seasonal factors influence quantal transmitter release and calcium dependence at amphibian neuromuscular junctions.

Authors:  Dengyun Ge; Nickolas Lavidis
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2017-06-21       Impact factor: 3.619

Review 5.  Zebrafish neuromuscular junction: The power of N.

Authors:  Paul Brehm; Hua Wen
Journal:  Neurosci Lett       Date:  2019-09-23       Impact factor: 3.046

6.  Localizing quantal currents along frog neuromuscular junctions.

Authors:  W Van der Kloot; L A Naves
Journal:  J Physiol       Date:  1996-11-15       Impact factor: 5.182

7.  Kinetics, Ca2+ dependence, and biophysical properties of integrin-mediated mechanical modulation of transmitter release from frog motor nerve terminals.

Authors:  B M Chen; A D Grinnell
Journal:  J Neurosci       Date:  1997-02-01       Impact factor: 6.167

8.  Role of calcium and vesicle-docking proteins in remobilising dormant neuromuscular junctions in desert frogs.

Authors:  Nickolas A Lavidis; Nicholas J Hudson; Peng T Choy; Sigrid A Lehnert; Craig E Franklin
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2007-11-07       Impact factor: 1.836

9.  Ca2+ dependence of the binomial parameters p and n at the mouse neuromuscular junction.

Authors:  Xueyong Wang; Martin J Pinter; Mark M Rich
Journal:  J Neurophysiol       Date:  2009-11-25       Impact factor: 2.714

10.  Probabilistic secretion of quanta from visualized sympathetic nerve varicosities in mouse vas deferens.

Authors:  N A Lavidis; M R Bennett
Journal:  J Physiol       Date:  1992-08       Impact factor: 5.182

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