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


     


J Neurophysiol 71: 1468-1479, 1994;
0022-3077/94 $5.00
This Article
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 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 Google Scholar
Google Scholar
Right arrow Articles by Hochman, S.
Right arrow Articles by McCrea, D. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hochman, S.
Right arrow Articles by McCrea, D. A.

Journal of Neurophysiology, Vol 71, Issue 4 1468-1479, Copyright © 1994 by APS


ARTICLES

Effects of chronic spinalization on ankle extensor motoneurons. II. Motoneuron electrical properties

S. Hochman and D. A. McCrea
Department of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

1. Intracellular recording and stimulation techniques were used in a comparison of electrical properties of triceps surae and plantaris motoneurons between unlesioned and 6-wk chronic spinal (L1-L2) cats. The primary analysis was restricted to 195 motoneurons with action potential heights > or = 80 mV. 2. Voltage transients resulting from short-duration current pulses (0.5 ms) were used to estimate membrane time constant (tau m) and equivalent cylinder electrotonic length (L). Although L was unchanged, tau m and the equalization phase time constant were significantly lower (17%) in motoneurons from chronic spinal preparations. Estimated total cell surface area was also reduced by 11%. The incidence of sag conductances, as judged from observations of the decay of voltage transients, increased from 3% to 29% after chronic spinalization. 3. Input resistance, as measured from either the amplitude of voltage responses to long-duration (50 ms) hyperpolarizing pulses (RinL) or from the area of the short-duration current pulse-induced voltage transients, was unchanged in the chronic spinal preparation. 4. Rheobase current was unchanged but threshold voltage (V Th) was increased in chronic spinal motoneurons. Increased V Th was not a result of membrane hyperpolarization because both mean action potential height (88 mV) and resting membrane potential (70 mV) were identical in both preparations. 5. The threshold current for action potential activation by short-duration (0.5 ms) current pulses increased 28% in chronic spinal preparations. This is consistent with the increase in V Th in the same motoneurons. 6. Measured V Th was identical to that calculated from the product of RinL and rheobase in the unlesioned preparation but was significantly larger than calculated V Th in chronic spinal preparations. This may indicate an increased incidence or magnitude of subthreshold rectification processes in motoneurons from chronic spinal preparations. These results in barbiturate-anesthetized preparations suggest that ankle extensor motoneurons are less excitable in the chronic spinal state. 7. Mean afterhyperpolarization duration was 10% shorter in motoneurons from chronic spinal preparations, whereas amplitude was unchanged. 8. Electrical properties were also compared in chronic spinal and unlesioned preparations using motoneurons with action potential heights of 60-79 mV. In these motoneurons with presumably poorer impalements there were no significant differences between unlesioned and chronic spinal preparations. 9. Ia monosynaptic excitatory postsynaptic potentials (EPSPs) recorded in the same motoneurons have decreased half-widths and rise times and increased amplitudes.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
D. Farina, M. Pozzo, M. Lanzetta, and R. M. Enoka
Discharge Variability of Motor Units in an Intrinsic Muscle of Transplanted Hand
J Neurophysiol, May 1, 2008; 99(5): 2232 - 2240.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
D. C. Button, J. M. Kalmar, K. Gardiner, T. Marqueste, H. Zhong, R. R. Roy, V. R. Edgerton, and P. F. Gardiner
Does elimination of afferent input modify the changes in rat motoneurone properties that occur following chronic spinal cord transection?
J. Physiol., January 15, 2008; 586(2): 529 - 544.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
S. M. ElBasiouny and V. K. Mushahwar
Suppressing the excitability of spinal motoneurons by extracellularly applied electrical fields: insights from computer simulations
J Appl Physiol, November 1, 2007; 103(5): 1824 - 1836.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. C. Petruska, R. M. Ichiyama, D. L. Jindrich, E. D. Crown, K. E. Tansey, R. R. Roy, V. R. Edgerton, and L. M. Mendell
Changes in Motoneuron Properties and Synaptic Inputs Related to Step Training after Spinal Cord Transection in Rats
J. Neurosci., April 18, 2007; 27(16): 4460 - 4471.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
P. Gardiner, Y. Dai, and C. J. Heckman
Effects of exercise training on {alpha}-motoneurons
J Appl Physiol, October 1, 2006; 101(4): 1228 - 1236.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. G. Hornby, J. H. Kahn, M. Wu, and B. D. Schmit
Temporal facilitation of spastic stretch reflexes following human spinal cord injury
J. Physiol., March 15, 2006; 571(3): 593 - 604.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
S. M. ElBasiouny, D. J. Bennett, and V. K. Mushahwar
Simulation of Dendritic CaV1.3 Channels in Cat Lumbar Motoneurons: Spatial Distribution
J Neurophysiol, December 1, 2005; 94(6): 3961 - 3974.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
B. Cormery, E. Beaumont, K. Csukly, and P. Gardiner
Hindlimb unweighting for 2 weeks alters physiological properties of rat hindlimb motoneurones
J. Physiol., November 1, 2005; 568(3): 841 - 850.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Manuel, C. Meunier, M. Donnet, and D. Zytnicki
How Much Afterhyperpolarization Conductance Is Recruited by an Action Potential? A Dynamic-Clamp Study in Cat Lumbar Motoneurons
J. Neurosci., September 28, 2005; 25(39): 8917 - 8923.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M.-P. Cote and J.-P. Gossard
Step Training-Dependent Plasticity in Spinal Cutaneous Pathways
J. Neurosci., December 15, 2004; 24(50): 11317 - 11327.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
I. Zijdewind and C. K. Thomas
Motor Unit Firing During and After Voluntary Contractions of Human Thenar Muscles Weakened by Spinal Cord Injury
J Neurophysiol, April 1, 2003; 89(4): 2065 - 2071.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
J. E. Butler and C. K. Thomas
Effects of sustained stimulation on the excitability of motoneurons innervating paralyzed and control muscles
J Appl Physiol, February 1, 2003; 94(2): 567 - 575.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M.-C. Perreault
Motoneurons Have Different Membrane Resistance during Fictive Scratching and Weight Support
J. Neurosci., September 15, 2002; 22(18): 8259 - 8265.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. J. Bennett, Y. Li, and M. Siu
Plateau Potentials in Sacrocaudal Motoneurons of Chronic Spinal Rats, Recorded In Vitro
J Neurophysiol, October 1, 2001; 86(4): 1955 - 1971.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. M. Macpherson and J. Fung
Weight Support and Balance During Perturbed Stance in the Chronic Spinal Cat
J Neurophysiol, December 1, 1999; 82(6): 3066 - 3081.
[Abstract] [Full Text] [PDF]




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