JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 83: 146-155, 2000;
0022-3077/00 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (11)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Juranek, J.
Right arrow Articles by Currie, S. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Juranek, J.
Right arrow Articles by Currie, S. N.

The Journal of Neurophysiology Vol. 83 No. 1 January 2000, pp. 146-155
Copyright ©2000 by the American Physiological Society

Electrically Evoked Fictive Swimming in the Low-Spinal Immobilized Turtle

Jenifer Juranek and Scott N. Currie

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.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
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]


Home page
J. Neurophysiol.Home page
R. F. Samara and S. N. Currie
Location of Spinal Cord Pathways That Control Hindlimb Movement Amplitude and Interlimb Coordination During Voluntary Swimming in Turtles
J Neurophysiol, April 1, 2008; 99(4): 1953 - 1968.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. F. Samara and S. N. Currie
Crossed Commissural Pathways in the Spinal Hindlimb Enlargement Are Not Necessary for Right Left Hindlimb Alternation During Turtle Swimming
J Neurophysiol, October 1, 2007; 98(4): 2223 - 2231.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. Berkowitz
Spinal Interneurons That Are Selectively Activated during Fictive Flexion Reflex
J. Neurosci., April 25, 2007; 27(17): 4634 - 4641.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Berkowitz
Physiology and Morphology Indicate That Individual Spinal Interneurons Contribute to Diverse Limb Movements
J Neurophysiol, December 1, 2005; 94(6): 4455 - 4470.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
G. M. Earhart and P. S. G. Stein
Step, Swim, and Scratch Motor Patterns in the Turtle
J Neurophysiol, November 1, 2000; 84(5): 2181 - 2190.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
G. M. Earhart and P. S. G. Stein
Scratch-Swim Hybrids in the Spinal Turtle: Blending of Rostral Scratch and Forward Swim
J Neurophysiol, January 1, 2000; 83(1): 156 - 165.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online