Literature DB >> 5145723

The time course of minimal excitory post-synaptic potentials evoked in spinal motoneurones by group Ia afferent fibres.

J J Jack, S Miller, R Porter, S J Redman.   

Abstract

1. Group Ia EPSPs were recorded from lumbosacral motoneurones in anaesthetized cats after almost complete section of the relevant dorsal roots. The EPSPs were usually of small amplitude (median value of 230 muV) and an averaging device was used to improve the definition of their time course.2. From a total of over 500 averaged EPSPs a smaller number (342) were subjected to analysis. The other EPSPs were rejected either because they showed signs of multiple origin in the rising phase of their time course (see Methods) or because the resting membrane potential of the cell was less than 50 mV. All the selected EPSPs had their rise time (from the 10 to the 90% level) and half-width measured, and a semilogarithmic plot of their decay time course was made.3. 252 of the EPSPs showed an exponential decline in their later time course and the slope of this line was used to give an estimate of the membrane time constant. The range of the time constant for different motoneurones was 2.3-12.9 msec, with a mean value of 5.8 msec.4. In ten cells an EPSP was recorded which was judged to be generated exclusively by synaptic knobs located on the soma. On this assumption measurements of the normalized rise time, half-width and break point time were used to estimate alpha, rho(infinity) and L by the method suggested in Jack & Redman (1971b). The estimated value of alpha ranged from 18 to 65. A positive correlation was found between alpha and tau(m), indicating that for these EPSPs the duration of current injection was independent of the membrane time constant. The peak time of the wave form of current injection was between 0.1 and 0.25 msec. The estimates of rho(infinity) were not thought to be very accurate. A lower limit of 4 was assumed and the highest measured value was 12, but in three cells the time course of the EPSP could not be fitted even with a very high value of rho(infinity). Some possible explanations for this discrepancy are mentioned in the Discussion. The electrotonic length of the dendrites (L) was usually greater than 1.0 lambda and ranged between 0.75 and 1.5 lambda. Evidence for an open-circuit termination of the dendrites was found in some cells.5. The normalized values of the rise time and half-width were used to make an electrotonic distance allocation to the 246 EPSPs which were judged to be non-somatic. The method of allocation was not precise because individual values of rho(infinity) and L were not available for these motoneurones. Instead, a maximum possible range was assumed: for rho(infinity), 4-25; for L, 0.75-1.5. The range of alpha was also assumed, from 12 to 100. With these values the motoneurone model (Jack & Redman, 1971b) was used to set limits within which the normalized rise time and half-width of all EPSPs, generated by current at a single point, should lie. Twenty of the 246 EPSPs lay outside these boundary lines and hence they did not receive a distance allocation. The remaining 226 were assigned values between 0.2 and 1.6 lambda (in 0.2 lambda steps); the majority of the allocations (183) were to the proximal electrotonic part of the dendrites (0.2, 0.4 or 0.6 lambda). The relationship of these distance allocations to the histological results of Conradi (1969) is discussed.6. It is concluded that there is no good evidence against the view that the main time course of minimal Ia EPSPs can be explained by their generation by a brief pulse of synaptic current and subsequent passive spread.

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Year:  1971        PMID: 5145723      PMCID: PMC1331888          DOI: 10.1113/jphysiol.1971.sp009474

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


  19 in total

1.  Anatomical organization of the brachial spinal cord of the cat. II. The motoneuron plexus.

Authors:  P Sterling; H G Kuypers
Journal:  Brain Res       Date:  1967-02       Impact factor: 3.252

2.  The relative densities of monosynaptic pathways to the cell bodies and dendrites of the cat ventral horn.

Authors:  L Illis
Journal:  J Neurol Sci       Date:  1967 Mar-Apr       Impact factor: 3.181

3.  Anatomical organization of the brachial spinal cord of the cat. I. The distribution of dorsal root fibers.

Authors:  P Sterling; H G Kuypers
Journal:  Brain Res       Date:  1967-02       Impact factor: 3.252

4.  Terminals of single Ia fibers: distribution within a pool of 300 homonymous motor neurons.

Authors:  L M Mendell; E Henneman
Journal:  Science       Date:  1968-04-05       Impact factor: 47.728

5.  Dendritic location of synapses and possible mechanisms for the monosynaptic EPSP in motoneurons.

Authors:  W Rall; R E Burke; T G Smith; P G Nelson; K Frank
Journal:  J Neurophysiol       Date:  1967-09       Impact factor: 2.714

6.  Electrical behaviour of the motoneurone membrane during intracellularly applied current steps.

Authors:  M Ito; T Oshima
Journal:  J Physiol       Date:  1965-10       Impact factor: 5.182

7.  Distinguishing theoretical synaptic potentials computed for different soma-dendritic distributions of synaptic input.

Authors:  W Rall
Journal:  J Neurophysiol       Date:  1967-09       Impact factor: 2.714

8.  Composite nature of the monosynaptic excitatory postsynaptic potential.

Authors:  R E Burke
Journal:  J Neurophysiol       Date:  1967-09       Impact factor: 2.714

9.  Group Ia synaptic input to fast and slow twitch motor units of cat triceps surae.

Authors:  R E Burke
Journal:  J Physiol       Date:  1968-06       Impact factor: 5.182

10.  Analysis of synaptic efficacy in spinal motoneurones from 'quantum' aspects.

Authors:  M Kuno; J T Miyahara
Journal:  J Physiol       Date:  1969-04       Impact factor: 5.182

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  88 in total

1.  Signals in stochastically generated neurons.

Authors:  J L Winslow; S F Jou; S Wang; J M Wojtowicz
Journal:  J Comput Neurosci       Date:  1999-01       Impact factor: 1.621

2.  Integration of function in the nervous system - a new theory.

Authors:  J Dempsher
Journal:  Acta Biotheor       Date:  1979       Impact factor: 1.774

3.  The relative unimportance of the temporal pattern of the primary afferent input in determining the mean level of motor firing in the tonic vibration reflex.

Authors:  P B Matthews
Journal:  J Physiol       Date:  1975-10       Impact factor: 5.182

4.  Estimating the location and time course of synaptic input from multi-site potential recordings.

Authors:  Steven J Cox
Journal:  J Comput Neurosci       Date:  2004 Sep-Oct       Impact factor: 1.621

5.  Synaptic potentials evoked in cat dorsal spinocerebellar tract neurones by impulses in single group I muscle afferents.

Authors:  B Walmsley
Journal:  J Physiol       Date:  1989-08       Impact factor: 5.182

6.  Presynaptic inhibition of synaptic potentials evoked in cat spinal motoneurones by impulses in single group Ia axons.

Authors:  J D Clements; I D Forsythe; S J Redman
Journal:  J Physiol       Date:  1987-02       Impact factor: 5.182

7.  Reduction by general anaesthetics of group Ia excitatory postsynaptic potentials and currents in the cat spinal cord.

Authors:  D M Kullmann; R L Martin; S J Redman
Journal:  J Physiol       Date:  1989-05       Impact factor: 5.182

8.  An in vivo pharmacological study of single group Ia fibre contacts with motoneurones in the cat spinal cord.

Authors:  B Walmsley; P S Bolton
Journal:  J Physiol       Date:  1994-12-15       Impact factor: 5.182

9.  Projections of pyramidal tract cells to alpha-motoneurones innervating hind-limb muscles in the monkey.

Authors:  E Jankowska; Y Padel; R Tanaka
Journal:  J Physiol       Date:  1975-08       Impact factor: 5.182

10.  Synchronization of motor unit activity during voluntary contraction in man.

Authors:  A K Datta; J A Stephens
Journal:  J Physiol       Date:  1990-03       Impact factor: 5.182

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