|
|
||||||||
Journal of Neurophysiology, Vol 75, Issue 5 1815-1825, Copyright © 1996 by APS
ARTICLES |
S. R. Soffe
School of Biological Sciences, University of Bristol, United Kingdom.
1. Mechanisms underlying the selective expression of different motor patterns in vertebrates are poorly understood. Immobilized, spinal Xenopus embryos are used here to examine the motor patterns evoked by various concentrations of excitatory amino acids. 2. Relatively low concentrations of N-methyl-D-aspartate (NMDA) (40-60 microM), kainate (7-8 microM), and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) (5 microM) evoked motor root discharge characteristic of swimming. Brief applications of higher concentrations of kainate (20-40 microM), AMPA (25-30 microM), quisqualate (5 microM), and glutamate (1-4 mM) evoked sequences of a different motor pattern: struggling. This is characterized by a longer cycle period, increased burst duration, and a reversed longitudinal pattern of motor root discharge. The struggling pattern was never evoked by higher concentrations of NMDA (300-500 microM), but was evoked by 30 microM AMPA or 5 microM quisqualate in the presence of 50 microM D-2-amino-5-phosphonopentanoic acid. 3. Intracellular recordings from presumed spinal motoneurons showed different patterns of activity during agonist-evoked swimming and struggling. The patterns were like those described previously during sensory-evoked behavior. 4. Caudal applications of excitatory amino acids that produced struggling discharge did so only at caudal motor roots, whereas caudal applications of NMDA evoked swimming activity throughout the spinal cord. 5. During excitatory-amino-acid-evoked struggling, sensory Rohon-Beard neurons depolarized up to 7 mV, but did not fire. 6. The results show that expression of the struggling pattern, like swimming, is not critically dependent on sensory discharge. The results are also consistent with the idea that expression of the two very different motor patterns for swimming or struggling in this simple vertebrate preparation can be controlled by the level of excitation within the spinal motor circuitry, and need not involve the activity of a specific external neuromodulator.
This article has been cited by other articles:
![]() |
S. R. Soffe, A. Roberts, and W.-C. Li Defining the excitatory neurons that drive the locomotor rhythm in a simple vertebrate: insights into the origin of reticulospinal control J. Physiol., October 15, 2009; 587(20): 4829 - 4844. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Berkowitz Physiology and Morphology of Shared and Specialized Spinal Interneurons for Locomotion and Scratching J Neurophysiol, June 1, 2008; 99(6): 2887 - 2901. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-C. Li, B. Sautois, A. Roberts, and S. R. Soffe Reconfiguration of a Vertebrate Motor Network: Specific Neuron Recruitment and Context-Dependent Synaptic Plasticity J. Neurosci., November 7, 2007; 27(45): 12267 - 12276. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. Merrywest, D. L. McLean, J. T. Buchanan, and K. T. Sillar Evolutionary Divergence in Developmental Strategies and Neuromodulatory Control Systems of Two Amphibian Locomotor Networks Integr. Comp. Biol., February 1, 2004; 44(1): 47 - 56. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. F. Rast Nitric oxide induces centrally generated motor patterns in the locust suboesophageal ganglion J. Exp. Biol., January 11, 2001; 204(21): 3789 - 3801. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Prime, Y. Pichon, and L. E. Moore N-Methyl-D-Aspartate-Induced Oscillations in Whole Cell Clamped Neurons From the Isolated Spinal Cord of Xenopus laevis Embryos J Neurophysiol, August 1, 1999; 82(2): 1069 - 1073. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. D. Milner and L. T. Landmesser Cholinergic and GABAergic Inputs Drive Patterned Spontaneous Motoneuron Activity before Target Contact J. Neurosci., April 15, 1999; 19(8): 3007 - 3022. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Saltiel, M. C. Tresch, and E. Bizzi Spinal Cord Modular Organization and Rhythm Generation: An NMDA Iontophoretic Study in the Frog J Neurophysiol, November 1, 1998; 80(5): 2323 - 2339. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Juranek and W. Metzner Segregation of Behavior-Specific Synaptic Inputs to a Vertebrate Neuronal Oscillator J. Neurosci., November 1, 1998; 18(21): 9010 - 9019. [Abstract] [Full Text] [PDF] |
||||
![]() |
F.-Y. Zhao, E. Wolf, and A. Roberts Longitudinal distribution of components of excitatory synaptic input to motoneurones during swimming in young Xenopus tadpoles: experiments with antagonists J. Physiol., September 15, 1998; 511(3): 887 - 901. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. M. Kuenzi and N. Dale The Pharmacology and Roles of two K+ Channels in Motor Pattern Generation in the Xenopus Embryo J. Neurosci., February 15, 1998; 18(4): 1602 - 1612. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |