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


     


J Neurophysiol 87: 1094-1105, 2002;
0022-3077/02 $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 (15)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Demir, R.
Right arrow Articles by Ziskind-Conhaim, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Demir, R.
Right arrow Articles by Ziskind-Conhaim, L.

The Journal of Neurophysiology Vol. 87 No. 2 February 2002, pp. 1094-1105
Copyright ©2002 by the American Physiological Society

Interactions Between Multiple Rhythm Generators Produce Complex Patterns of Oscillation in the Developing Rat Spinal Cord

Rezan Demir, Bao-Xi Gao, Meyer B. Jackson, and Lea Ziskind-Conhaim

Department of Physiology and Center for Neuroscience, University of Wisconsin Medical School, Madison, Wisconsin 53706

Demir, Rezan, Bao-Xi Gao, Meyer B. Jackson, and Lea Ziskind-Conhaim. Interactions Between Multiple Rhythm Generators Produce Complex Patterns of Oscillation in the Developing Rat Spinal Cord. J. Neurophysiol. 87: 1094-1105, 2002. Neural networks capable of generating coordinated rhythmic activity form at early stages of development in the spinal cord. In this study, voltage-imaging techniques were used to examine the spatiotemporal pattern of rhythmic activity in transverse slices of lumbar spinal cord from embryonic and neonatal rats. Real-time images were recorded in slices stained with the voltage-sensitive fluorescent dye RH414 using a 464-element photodiode array. Fluorescence signals showed spontaneous voltage oscillations with a frequency of 3 Hz. Simultaneous recordings of fluorescence and extracellular field potential demonstrated that the two signals oscillated with the same frequency and had a distinct phase relationship, indicating that the fluorescence changes represented changes in transmembrane potentials. The oscillations were reversibly blocked by cobalt (1 mM), indicating a dependence on Ca2+ influx through voltage-gated Ca2+ channels. Extracellular field potentials revealed oscillations with the same frequency in both stained and unstained slices. Oscillations were apparent throughout a slice, although their amplitudes varied in different regions. The largest amplitude oscillations were produced in the lateral regions. To examine the spatial organization of rhythm-generating networks, slices were cut into halves and quarters. Each fragment continued to oscillate with the same frequency as intact slices but with smaller amplitudes. This finding suggested that rhythm-generating networks were widely distributed and did not depend on long-range projections. In slices from neonatal rats, the oscillations exhibited a complex spatiotemporal pattern, with depolarizations alternating between mirror locations in the right and left sides of the cord. Furthermore, within each side depolarizations alternated between the lateral and medial regions. This medial-lateral pattern was preserved in hemisected slices, indicating that pathways intrinsic to each side coordinated this activity. A different pattern of oscillation was observed in slices from embryos with synchronous 3-Hz oscillations occurring in limited regions. Our study demonstrated that rhythm generators were distributed throughout transverse sections of the lumbar spinal cord and exhibited a complex spatiotemporal pattern of coordinated rhythmic activity.




This article has been cited by other articles:


Home page
J. Physiol.Home page
A. Nistri, K. Ostroumov, E. Sharifullina, and G. Taccola
Tuning and playing a motor rhythm: how metabotropic glutamate receptors orchestrate generation of motor patterns in the mammalian central nervous system
J. Physiol., April 15, 2006; 572(2): 323 - 334.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. Ziskind-Conhaim and S. Redman
Spatiotemporal Patterns of Dorsal Root-Evoked Network Activity in the Neonatal Rat Spinal Cord: Optical and Intracellular Recordings
J Neurophysiol, September 1, 2005; 94(3): 1952 - 1961.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
W. J. Moody and M. M. Bosma
Ion Channel Development, Spontaneous Activity, and Activity-Dependent Development in Nerve and Muscle Cells
Physiol Rev, July 1, 2005; 85(3): 883 - 941.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. U. R. Asghar, P. F. Cilia La Corte, F. E. N. LeBeau, M. A. Dawoud, S. C. Reilly, E. H. Buhl, M. A. Whittington, and A. E. King
Oscillatory activity within rat substantia gelatinosa in vitro: a role for chemical and electrical neurotransmission
J. Physiol., January 1, 2005; 562(1): 183 - 198.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
P. Darbon, A. Tscherter, C. Yvon, and J. Streit
Role of the Electrogenic Na/K Pump in Disinhibition-Induced Bursting in Cultured Spinal Networks
J Neurophysiol, November 1, 2003; 90(5): 3119 - 3129.
[Abstract] [Full Text] [PDF]




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