Literature DB >> 9017200

The binomial model in fluctuation analysis of quantal neurotransmitter release.

D M Quastel1.   

Abstract

The mathematics of the binomial model for quantal neurotransmitter release is considered in general terms, to explore what information might be extractable from statistical aspects of data. For an array of N statistically independent release sites, each with a release probability p, the compound binomial always pertains, with <m> = N<p>, p' identical to 1 - var(m)/<m> = <p> (1 + cvp2) and n' identical to <m>/p' = N/(1 + cvp2), where m is the output/stimulus and cvp2 is var(p)/<p>2. Unless n' is invariant with ambient conditions or stimulation paradigms, the simple binomial (cvp = 0) is untenable and n' is neither N nor the number of "active" sites or sites with a quantum available. At each site p = popA, whereas po is the output probability if a site is "eligible" or "filled" despite previous quantal discharge, and pA (eligibility probability) depends at least on the replenishment rate, po, and interstimulus time. Assuming stochastic replenishment, a simple algorithm allows calculation of the full statistical composition of outputs for any hypothetical combinations of po's and refill rates, for any stimulation paradigm and spontaneous release. A rise in n' (reduced cvp) tends to occur whenever po varies widely between sites, with a raised stimulation frequency or factors (tending to increase po's. Unlike <m> and var(m) at equilibrium, output changes early in trains of stimuli, and covariances, potentially provide information about whether changes in <m> reflect change in <po> or in <pA>. Formulae are derived for variance and third moments of postsynaptic responses, which depend on the quantal mix in the signals. A new, easily computed function, the area product, gives noise-unbiased variance of a series of synaptic signals and its peristimulus time distribution, which is modified by the unit channel composition of quantal responses and if the signals reflect mixed responses from synapses with different quantal time course.

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Year:  1997        PMID: 9017200      PMCID: PMC1185598          DOI: 10.1016/s0006-3495(97)78709-5

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  18 in total

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Authors:  T H Brown; D H Perkel; M W Feldman
Journal:  Proc Natl Acad Sci U S A       Date:  1976-08       Impact factor: 11.205

2.  Modeling of the quantal release at interneuronal synapses: analysis of permissible values of model moments.

Authors:  A E Dityatev; V M Kozhanov; S O Gapanovich
Journal:  J Neurosci Methods       Date:  1992-07       Impact factor: 2.390

3.  The relation between transmitter release and Ca2+ entry at the mouse motor nerve terminal: role of stochastic factors causing heterogeneity.

Authors:  D M Quastel; Y Y Guan; D A Saint
Journal:  Neuroscience       Date:  1992-12       Impact factor: 3.590

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Authors:  J I HUBBARD
Journal:  J Physiol       Date:  1963-12       Impact factor: 5.182

5.  THE MEASUREMENT OF SYNAPTIC DELAY, AND THE TIME COURSE OF ACETYLCHOLINE RELEASE AT THE NEUROMUSCULAR JUNCTION.

Authors:  B KATZ; R MILEDI
Journal:  Proc R Soc Lond B Biol Sci       Date:  1965-02-16

Review 6.  Quantal analysis and synaptic efficacy in the CNS.

Authors:  H Korn; D S Faber
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Authors:  S Redman
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8.  A quantitative study of end-plate potentials in isolated human muscle.

Authors:  D Elmqvist; D M Quastel
Journal:  J Physiol       Date:  1965-06       Impact factor: 5.182

9.  Quantal transmitter release mediated by strontium at the mouse motor nerve terminal.

Authors:  A I Bain; D M Quastel
Journal:  J Physiol       Date:  1992-05       Impact factor: 5.182

10.  Multiplicative and additive Ca(2+)-dependent components of facilitation at mouse endplates.

Authors:  A I Bain; D M Quastel
Journal:  J Physiol       Date:  1992-09       Impact factor: 5.182

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  37 in total

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Authors:  S Weis; R Schneggenburger; E Neher
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

2.  Implications of all-or-none synaptic transmission and short-term depression beyond vesicle depletion: a computational study.

Authors:  V Matveev; X J Wang
Journal:  J Neurosci       Date:  2000-02-15       Impact factor: 6.167

3.  Analysis and implications of equivalent uniform approximations of nonuniform unitary synaptic systems.

Authors:  V V Uteshev; J B Patlak; P S Pennefather
Journal:  Biophys J       Date:  2000-12       Impact factor: 4.033

4.  Separation of presynaptic and postsynaptic contributions to depression by covariance analysis of successive EPSCs at the calyx of Held synapse.

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5.  Estimating synaptic parameters from mean, variance, and covariance in trains of synaptic responses.

Authors:  V Scheuss; E Neher
Journal:  Biophys J       Date:  2001-10       Impact factor: 4.033

6.  Estimation of quantal size and number of functional active zones at the calyx of Held synapse by nonstationary EPSC variance analysis.

Authors:  A C Meyer; E Neher; R Schneggenburger
Journal:  J Neurosci       Date:  2001-10-15       Impact factor: 6.167

Review 7.  Presynaptic frequency- and pattern-dependent filtering.

Authors:  Alex M Thomson
Journal:  J Comput Neurosci       Date:  2003 Sep-Oct       Impact factor: 1.621

8.  Mechanisms of short-term plasticity at neuromuscular active zones of Drosophila.

Authors:  Stefan Hallermann; Manfred Heckmann; Robert J Kittel
Journal:  HFSP J       Date:  2010-04-08

9.  Proteolysis of SNARE proteins alters facilitation and depression in a specific way.

Authors:  Samuel M Young
Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-03       Impact factor: 11.205

10.  Release kinetics, quantal parameters and their modulation during short-term depression at a developing synapse in the rat CNS.

Authors:  Holger Taschenberger; Volker Scheuss; Erwin Neher
Journal:  J Physiol       Date:  2005-08-11       Impact factor: 5.182

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