Literature DB >> 7139344

Changes in MEPP and EPP amplitude distributions in the mouse diaphragm during synapse formation and degeneration.

C G Muniak, M E Kriebel, C G Carlson.   

Abstract

Miniature end-plate potential (MEPP) and end-plate potential (EPP) amplitude histograms were examined in the mouse diaphragm during degeneration, deterioration, re-innervation and neonatal development. MEPPs and EPPs were recorded with conventional electrophysiological techniques. Control MEPP amplitude distributions from mice 21-30 days old showed two classes of MEPPs. The larger class composed 80-90% of the MEPPs and formed a bell-shaped distribution (bell-MEPPs). The smaller class (skew-MEPPs) formed a skewed distribution with a peak 1/7 to 1/15 that of bell-MEPPs. Usually, MEPP amplitude distributions did not change during the course of nerve degeneration or during deterioration in the bath. MEPP amplitude distributions from newly re-innervated fibers were composed mainly of skew-MEPPs. At later stages of re-innervation the relative numbers of skew-MEPPs decreased. Many fibers from neonatal mice (2-3 days old) also showed mainly skew-MEPPs. Rise time vs amplitude plots were constructed from neonatal and re-innervating preparations. The skew-MEPP time-to-peak measurements fell on or below the regression line calculated from the time-to-peak data of the bell-MEPPs. This indicates that the skew-MEPPs originated from the same site as the bell-MEPPs. Unitary EPPs were recorded from neonatal and re-innervating preparations by reducing the evoked response with cobalt ions (4 mM). Distributions of unitary EPPs were similar to those of bell-MEPPs. It is concluded that there are two classes of spontaneous quanta. The skew-MEPP class dominates MEPP amplitude distributions during the early stages of re-innervation and early neonatal preparations. In all stages of development the unitary evoked EPPs have the same mean amplitude and time-to-peak as the bell-MEPPs. The data suggest that the skew class is not available for evoked release.

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Year:  1982        PMID: 7139344     DOI: 10.1016/0165-3806(82)90151-1

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  8 in total

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Authors:  Masazumi Takahashi; Tai Kubo; Akira Mizoguchi; C George Carlson; Katsuaki Endo; Katsunori Ohnishi
Journal:  EMBO Rep       Date:  2002-07       Impact factor: 8.807

2.  Depolarization-induced Ca2+ entry preferentially evokes release of large quanta in the developing Xenopus neuromuscular junction.

Authors:  Xiao-Ping Sun; Bo-Ming Chen; Olav Sand; Yoshi Kidokoro; Alan D Grinnell
Journal:  J Neurophysiol       Date:  2010-09-15       Impact factor: 2.714

3.  Neostigmine increases the size of subunits composing the quantum of transmitter release at mouse neuromuscular junction.

Authors:  C G Carlson; M E Kriebel
Journal:  J Physiol       Date:  1985-10       Impact factor: 5.182

4.  Morphological, physiological and biochemical observations on skate electric organ.

Authors:  G Q Fox; M E Kriebel; G D Pappas
Journal:  Anat Embryol (Berl)       Date:  1990

5.  Constitutive secretion of exogenous neurotransmitter by nonneuronal cells: implications for neuronal secretion.

Authors:  S Chang; R Girod; T Morimoto; M O'Donoghue; S Popov
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

6.  Subunit composition of the spontaneous miniature end-plate currents at the mouse neuromuscular junction.

Authors:  C Erxleben; M E Kriebel
Journal:  J Physiol       Date:  1988-06       Impact factor: 5.182

7.  Characteristics of spontaneous miniature and subminiature end-plate currents at the mouse neuromuscular junction.

Authors:  C Erxleben; M E Kriebel
Journal:  J Physiol       Date:  1988-06       Impact factor: 5.182

8.  Regulation of quantal shape by Rab3A: evidence for a fusion pore-dependent mechanism.

Authors:  Xueyong Wang; Ramachandran Thiagarajan; Qingbo Wang; Teclemichael Tewolde; Mark M Rich; Kathrin L Engisch
Journal:  J Physiol       Date:  2008-06-26       Impact factor: 5.182

  8 in total

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