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Vol. 281, Issue 3, 1381-1391, 1997
Department of Pharmacology, Faculty of Medicine, University of
Chile, Santiago, Chile (D.B., C.P.),
Laboratoire de
Neurophysiologie, Hôpital
Pitié-Salpétriêre, Paris, France (J.-C.W.), and
INSERM U161, Paris, France (D.L.B.)
A C-fiber reflex elicited by electrical stimulation within the
territory of the sural nerve was recorded from the ipsilateral biceps
femoris muscle in anesthetized rats. The temporal evolution of the
response was studied using a constant stimulus intensity (3 times
threshold), and recruitment curves were built by varying the stimulus
intensity from 0 to 7 times threshold. The intrathecal (i.t.) but not
i.c.v. administration of aspirin, indomethacin, ketoprofen and lysine
clonixinate resulted in dose-dependent depressions of the C-fiber
reflex. In contrast, saline was ineffective. Regardless of the route of
administration, the drugs never produced disturbances in heart rate
and/or acid-base equilibrium. When a constant level of stimulation was
used, 500 µg of aspirin i.t. induced a blockade of the reflex
immediately after the injection, followed by a partial recovery.
Indomethacin produced a stable depression, which reached 80 to 90%
with an i.t. dose of 500 µg. Ketoprofen and lysine clonixinate produced a more stable effect; the highest doses (500 µg) produced a
steady-state depression of approximately 50% for approximately 30 min.
When the recruitment curves were built with a range of nociceptive
stimulus intensities, all of the drugs except for indomethacin produced
a dose-dependent decrease in the slopes and the areas under the
recruitment curves without major modifications in the thresholds;
indomethacin also induced a significant dose-related increase in the
threshold. The orders of potency for both stimulation paradigms with
the i.t. route were the same, namely aspirin > indomethacin > lysine clonixinate
ketoprofen. It is concluded that
nonsteroidal anti-inflammatory drugs elicit significant antinociceptive effects at a spinal level, which do not depend on the existence of a
hyperalgesic or inflammatory state. Such effects were not seen after
injections within the lateral ventricle.