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J Neurophysiol 65: 468-476, 1991;
0022-3077/91 $5.00
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Journal of Neurophysiology, Vol 65, Issue 3 468-476, Copyright © 1991 by APS


ARTICLES

Strength-duration and activity-dependent excitability properties of frog afferent axons and their intraspinal projections

N. C. Tkacs and R. D. Wurster
Department of Physiology, Loyola University Medical Center, Maywood, Illinois 60153.

1. Excitability properties of afferent axons and terminal regions in frog dorsal roots (DR) and spinal cords in vitro were investigated by antidromic activation from three sites--the root, the entry zone (dorsal white matter or DW), and deep within the dorsal horn (DH)--while recordings were made from the DR. 2. Two approaches were used to assess physiological differences between telodendria and trunk axons. Rheobases and strength-duration time constants (tau sd) of single DR fibers were measured by stimulation in the DH or in the DW. Conduction velocity was estimated on the basis of onset latencies of evoked spikes (the time from stimulation to action potential arrival at the recording electrodes). Population supernormality was evaluated on the basis of responses to conditioned and unconditioned submaximal stimuli delivered to the DH or to the proximal end of isolated DRs. 3. Single-fiber action potentials occurred at longer latencies after DH stimulation than after DW stimulation. Estimated intraspinal conduction velocity was congruent to 0.6 m/s. Extraspinal conduction velocity in these fibers averaged 22.2 m/s. Average tau sd was longer in the DH than in the DW (670 microseconds vs. 204 microseconds). 4. DH and DR test responses evoked 10-150 ms after a conditioning stimulus had increased areas relative to unconditioned test responses. Conditioning-associated changes in evoked responses were greater with the DH stimulation site than with the DR stimulation site, and these changes were not altered by treatment designed to block synaptic transmission. 5. We conclude that membrane properties determining tau sd differ between large afferent axons and fine terminal regions of those axons.(ABSTRACT TRUNCATED AT 250 WORDS)





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