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The Journal of Neuroscience, June 1, 2003, 23(11):4766-4774
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Fatigue and Paradoxical Enhancement of Heat Response in C-Fiber Nociceptors from Cross-Modal Excitation
Yuan B. Peng,1
Matthias Ringkamp,1
Richard A. Meyer,1,2 and
James N. Campbell1,2
1 Department of Neurosurgery, School of Medicine, Johns Hopkins University,
Baltimore, Maryland 21287, and
2 Johns Hopkins Applied Physics Laboratory, Laurel, Maryland 20723
Fatigue refers to the decrement of response seen with repeated stimulation
and is a prominent attribute of nociceptors. Whether fatigue in nociceptors
involves transduction, spike initiation, or conduction mechanisms is unknown.
We investigated systematically how electrical, mechanical, and heat
conditioning stimuli (eCS, mCS, hCS) affected the subsequent response to a
test-heat stimulus applied 5 sec later to the receptive field of cutaneous
nociceptors. Standard teased-fiber techniques were used to record from
mechanoheat-sensitive C-fiber afferents in the anesthetized monkey. The
eCS was applied to the nerve trunk, whereas the hCS and mCS were applied to
the heat-test site. For the eCS, the number of pulses rather than frequency of
stimulation determined the level of fatigue. Fatigue varied inversely with the
time interval between the eCS and the test stimulus. For comparable responses
from the CS, the magnitude of fatigue was less after the mCS than after the
eCS. The mCS (but not the eCS) sometimes evoked a paradoxical increase in
response to the test-heat stimulus. Recovery from fatigue was significantly
faster after the eCS and mCS than the hCS. The paradoxical enhancement after
the mCS probably results from temporal summation of generator potentials
produced by mechanical and heat stimulation and suggests that the time
constant of the generator potential is on the order of seconds. Concurrent
enhancementfatigue effects may also explain why fatigue was less after
the mCS than the eCS. The dependency of recovery from fatigue on the modality
of the CS suggests that fatigue results from transductionspike
initiation mechanisms.
Key words: pain; somatosensory system; primary afferents; adaptation; fatigue; sensitization; nociceptors
Received Sep. 10, 2002;
revised Jan. 16, 2003;
accepted Mar. 14, 2003.
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