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The Journal of Neurophysiology Vol. 83 No. 1 January 2000, pp. 146-155
Copyright ©2000 by the American Physiological Society
Department of Neuroscience, University of California, Riverside, California 92521
Juranek, Jenifer and
Scott N. Currie.
Electrically Evoked Fictive Swimming in the Low-Spinal
Immobilized Turtle. J. Neurophysiol. 83: 146-155, 2000. Fictive swimming was elicited in low-spinal
immobilized turtles by electrically stimulating the contralateral
dorsolateral funiculus (cDLF) at the level of the third postcervical
segment (D3). Fictive hindlimb motor output was recorded as
electroneurograms (ENGs) from up to five peripheral nerves on the right
side, including three knee extensors (KE; iliotibialis [IT]-KE,
ambiens [AM]-KE, and femorotibialis [FT]-KE), a hip flexor (HF),
and a hip extensor (HE). Quantitative analyses of burst amplitude, duty
cycle and phase were used to demonstrate the close similarity of these
cDLF-evoked fictive motor patterns with previous myographic recordings
obtained from the corresponding hindlimb muscles during actual
swimming. Fictive rostral scratching was elicited in the same animals
by cutaneous stimulation of the shell bridge, anterior to the hindlimb. Fictive swim and rostral scratch motor patterns displayed similar phasing in hip and knee motor pools but differed in the relative amplitudes and durations of ENG bursts. Both motor patterns exhibited alternating HF and HE discharge, with monoarticular knee extensor (FT-KE) discharge during the late HF phase. The two motor patterns differed principally in the relative amplitudes and durations of HF and
HE bursts. Swim cycles were dominated by large-amplitude, long-duration
HE bursts, whereas rostral scratch cycles were dominated by
large-amplitude, long-duration HF discharge. Small but significant differences were also observed during the two behaviors in the onset
phase of biarticular knee extensor bursts (IT-KE and AM-KE) within each
hip cycle. Finally, interactions between swim and scratch motor
networks were investigated. Brief activation of the rostral scratch
during an ongoing fictive swim episode could insert one or more scratch
cycles into the swim motor pattern and permanently reset the burst
rhythm. Similarly, brief swim stimulation could interrupt and reset an
ongoing fictive rostral scratch. This shows that there are strong
central interactions between swim and scratch neural networks and
suggests that they may share key neural elements.
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