|
|
||||||||
Journal of Neurophysiology, Vol 71, Issue 6 2281-2293, Copyright © 1994 by APS
ARTICLES |
C. J. Heckman, J. F. Miller, M. Munson, K. D. Paul and W. Z. Rymer
Veterans Administration, Lakeside Hospital, Chicago, Illinois.
1. Steady-state postsynaptic potentials (PSPs) were generated by prolonged (approximately 1 s) high-frequency (100-200 Hz) electrical stimulation of nerves in the cat hindlimb. The characteristics of these steady-state PSPs were compared for two polysynaptic afferent pathways (ipsilateral cutaneous sural vs. contralateral peroneal nerves), two animal preparations (decerebrate vs. chloralose), and two motoneuron pools (medial gastrocnemius vs. lateral gastrocnemius-soleus). 2. PSPs from both nerves usually (36 of 51 cases) contained a mixture of depolarizing and hyperpolarizing components. In all 36 cases where the PSP contained a hyperpolarizing component, a consistent qualitative pattern emerged during prolonged stimulation: the hyperpolarization reached a peak approximately 20 ms after stimulation onset and then decayed with a biphasic time course that consisted of an initial rapid phase (20-40 ms) and a later slower phase (200-400 ms) before the steady-state value was reached. This pattern occurred regardless of the differences in polysynaptic afferent pathways, animal preparations, and motoneuron pools. 3. The consistency of this overall pattern was remarkable, given the existence of several quantitative differences among the PSPs. These differences include the following: hyperpolarizing components were least common in the sural and peroneal PSPs in the decerebrate preparation. And only these sural and peroneal PSPs tended to have prolonged afterpotentials after stimulus cessation. The steady-state sural PSPs in the decerebrate preparation tended to generate the largest PSPs and, moreover, these PSPs did not follow the overall trend of having a statistically significant relation between the amplitude of the initial hyperpolarization and the amount of its decay. Finally, transient sural PSPs in lateral gastrocnemius-soleus motoneurons in the decerebrate preparation tended to have the largest hyperpolarizations. 4. To determine whether the decay of the hyperpolarization and the subsequent dominance of depolarization was due to a decreased inhibition or an increased excitation, injected current pulses were utilized to measure the changes in the cell's input resistance during the course of the synaptic input. A strong decrease in input resistance accompanied the initial period of maximal hyperpolarization (50% with respect to the resting input resistance). Input resistance then returned toward resting values as hyperpolarization faded and depolarization became dominant. However, there remained a persistent decrease in input resistance during the final phase of the PSP that amounted to < 10% of the initial decrease. These findings indicated that much of the reduction in hyperpolarization reflected a progressive decrease in synaptic efficacy for the inhibition.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
A. S. Hyngstrom, M. D. Johnson, and C. J. Heckman Summation of Excitatory and Inhibitory Synaptic Inputs by Motoneurons With Highly Active Dendrites J Neurophysiol, April 1, 2008; 99(4): 1643 - 1652. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. G. Maltenfort, C. A. Phillips, M. L. McCurdy, and T. M. Hamm Determination of the Location and Magnitude of Synaptic Conductance Changes in Spinal Motoneurons by Impedance Measurements J Neurophysiol, September 1, 2004; 92(3): 1400 - 1416. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Bennett, L. Sanelli, C. L. Cooke, P. J. Harvey, and M. A. Gorassini Spastic Long-Lasting Reflexes in the Awake Rat After Sacral Spinal Cord Injury J Neurophysiol, May 1, 2004; 91(5): 2247 - 2258. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. J. Kuo, R. H. Lee, M. D. Johnson, H. M. Heckman, and C. J. Heckman Active Dendritic Integration of Inhibitory Synaptic Inputs In Vivo J Neurophysiol, December 1, 2003; 90(6): 3617 - 3624. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. H. Wilmink and T. R. Nichols Distribution of Heterogenic Reflexes Among the Quadriceps and Triceps Surae Muscles of the Cat Hind Limb J Neurophysiol, October 1, 2003; 90(4): 2310 - 2324. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. F. Prather, B. D. Clark, and T. C. Cope Firing Rate Modulation of Motoneurons Activated by Cutaneous and Muscle Receptor Afferents in the Decerebrate Cat J Neurophysiol, October 1, 2002; 88(4): 1867 - 1879. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. K. Haftel, J. F. Prather, C. J. Heckman, and T. C. Cope Recruitment of Cat Motoneurons in the Absence of Homonymous Afferent Feedback J Neurophysiol, August 1, 2001; 86(2): 616 - 628. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Lee and C. J. Heckman Adjustable Amplification of Synaptic Input in the Dendrites of Spinal Motoneurons In Vivo J. Neurosci., September 1, 2000; 20(17): 6734 - 6740. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Duysens, F. Clarac, and H. Cruse Load-Regulating Mechanisms in Gait and Posture: Comparative Aspects Physiol Rev, January 1, 2000; 80(1): 83 - 133. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Lee and C. J. Heckman Enhancement of Bistability in Spinal Motoneurons In Vivo by the Noradrenergic alpha 1 Agonist Methoxamine J Neurophysiol, May 1, 1999; 81(5): 2164 - 2174. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. R. Nichols Receptor Mechanisms Underlying Heterogenic Reflexes Among the Triceps Surae Muscles of the Cat J Neurophysiol, February 1, 1999; 81(2): 467 - 478. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. H. Lee and C. J. Heckman Bistability in Spinal Motoneurons In Vivo: Systematic Variations in Rhythmic Firing Patterns J Neurophysiol, August 1, 1998; 80(2): 572 - 582. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |