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The Journal of Neurophysiology Vol. 86 No. 3 September 2001, pp. 1481-1498
Copyright ©2001 by the American Physiological Society
Laboratory of Neural Control, Section on Developmental Neurobiology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892
Wenner, Peter and
Michael J. O'Donovan.
Mechanisms That Initiate Spontaneous Network Activity in the
Developing Chick Spinal Cord. J. Neurophysiol. 86: 1481-1498, 2001. Many developing networks exhibit a transient period of
spontaneous activity that is believed to be important developmentally. Here we investigate the initiation of spontaneous episodes of rhythmic
activity in the embryonic chick spinal cord. These episodes recur
regularly and are separated by quiescent intervals of many minutes. We
examined the role of motoneurons and their intraspinal synaptic targets
(R-interneurons) in the initiation of these episodes. During the latter
part of the inter-episode interval, we recorded spontaneous,
transient ventral root depolarizations that were accompanied by small,
spatially diffuse fluorescent signals from interneurons retrogradely
labeled with a calcium-sensitive dye. A transient often could be
resolved at episode onset and was accompanied by an intense pre-episode
(~500 ms) motoneuronal discharge (particularly in adductor and
sartorius) but not by interneuronal discharge monitored from the
ventrolateral funiculus (VLF). An important role for this pre-episode
motoneuron discharge was suggested by the finding that electrical
stimulation of motor axons, sufficient to activate R-interneurons,
could trigger episodes prematurely. This effect was mediated through
activation of R-interneurons because it was prevented by
pharmacological blockade of either the cholinergic motoneuronal inputs
to R-interneurons or the GABAergic outputs from R-interneurons to other
interneurons. Whole-cell recording from R-interneurons and imaging of
calcium dye-labeled interneurons established that R-interneuron cell
bodies were located dorsomedial to the lateral motor column
(R-interneuron region). This region became active before other labeled
interneurons when an episode was triggered by motor axon
stimulation. At the beginning of a spontaneous episode, whole-cell
recordings revealed that R-interneurons fired a high-frequency burst
of spikes and optical recordings demonstrated that the R-interneuron
region became active before other labeled interneurons. In the presence
of cholinergic blockade, however, episode initiation slowed and the
inter-episode interval lengthened. In addition, optical activity
recorded from the R-interneuron region no longer led that of other
labeled interneurons. Instead the initial activity occurred bilaterally
in the region medial to the motor column and encompassing the
central canal. These findings are consistent with the hypothesis that
transient depolarizations and firing in motoneurons, originating from
random fluctuations of interneuronal synaptic activity, activate
R-interneurons, which then trigger the recruitment of the rest of the
spinal interneuronal network. This unusual function for R-interneurons
is likely to arise because the output of these interneurons is
functionally excitatory during development.
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