Literature DB >> 12106261

The Isolation and Identification of Spinal Neurons That Control Movement in the Xenopus Embryo.

Nicholas Dale1.   

Abstract

A procedure for isolating spinal neurons of the Xenopus embryo has been devised. Using a variety of methods four of the eight previously described categories of neuron can be distinguished in vitro. Firstly, since many anatomical features of the neurons survived dissociation, sensory neurons and glycinergic inhibitory interneurons could be identified after isolation using anatomical criteria. Secondly, by selective labelling of the neurons in the intact spinal cord with fluorescein-conjugated dextran amines prior to dissociation, three classes of isolated neuron could be identified: motoneurons, putative excitatory interneurons and, once again, inhibitory interneurons. The identity of the inhibitory interneurons has been confirmed using glycine immunocytochemistry. The physiological properties of the isolated neurons were similar to those of their in vivo counterparts. The dissociated neurons exhibited strong membrane accommodation and outward rectification, both of which could be blocked by the injection of Cs+ ions. The neurons also retained their receptors for the agonists N-methyl-d-aspartate, kainate, quisqualate, glycine and GABA. Both the membrane properties and pharmacological sensitivity of the isolated neurons therefore appeared to be unaltered by the dissociation procedure. Thus the four classes of neuron from the Xenopus embryonic nervous system that can be identified after isolation constitute the basis for a valid model for detailed study of how the properties of individual neurons contribute to the functioning of the circuitry that underlies locomotor pattern generation in vertebrates.

Entities:  

Year:  1991        PMID: 12106261     DOI: 10.1111/j.1460-9568.1991.tb00039.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  17 in total

1.  Spike-independent release of ATP from Xenopus spinal neurons evoked by activation of glutamate receptors.

Authors:  Paul Brown; Nicholas Dale
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

2.  Modulation of K(+) currents in Xenopus spinal neurons by p2y receptors: a role for ATP and ADP in motor pattern generation.

Authors:  Paul Brown; Nicholas Dale
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

3.  Kinetic characterization of the voltage-gated currents possessed by Xenopus embryo spinal neurons.

Authors:  N Dale
Journal:  J Physiol       Date:  1995-12-01       Impact factor: 5.182

4.  Experimentally derived model for the locomotor pattern generator in the Xenopus embryo.

Authors:  N Dale
Journal:  J Physiol       Date:  1995-12-01       Impact factor: 5.182

5.  Simulation and parameter estimation study of a simple neuronal model of rhythm generation: role of NMDA and non-NMDA receptors.

Authors:  J Tabak; L E Moore
Journal:  J Comput Neurosci       Date:  1998-05       Impact factor: 1.621

6.  G-proteins are involved in 5-HT receptor-mediated modulation of N- and P/Q- but not T-type Ca2+ channels.

Authors:  Q Q Sun; N Dale
Journal:  J Neurosci       Date:  1999-02-01       Impact factor: 6.167

7.  Serotonergic inhibition of the T-type and high voltage-activated Ca2+ currents in the primary sensory neurons of Xenopus larvae.

Authors:  Q Q Sun; N Dale
Journal:  J Neurosci       Date:  1997-09-15       Impact factor: 6.167

8.  Nicotinic and muscarinic ACh receptors in rhythmically active spinal neurones in the Xenopus laevis embryo.

Authors:  R Perrins; A Roberts
Journal:  J Physiol       Date:  1994-07-15       Impact factor: 5.182

9.  Differential inhibition of N and P/Q Ca2+ currents by 5-HT1A and 5-HT1D receptors in spinal neurons of Xenopus larvae.

Authors:  Q Q Sun; N Dale
Journal:  J Physiol       Date:  1998-07-01       Impact factor: 5.182

10.  Composition of the excitatory drive during swimming in two amphibian embryos: Rana and Bufo.

Authors:  R Perrins; S R Soffe
Journal:  J Comp Physiol A       Date:  1996-10       Impact factor: 1.836

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