Vv. Romita et al., INTENSE PERIPHERAL ELECTRICAL-STIMULATION EVOKES BRIEF AND PERSISTENTINHIBITION OF THE NOCICEPTIVE TAIL WITHDRAWAL REFLEX IN THE RAT, Brain research, 761(2), 1997, pp. 192-202
In a study of modulation of nociception by sensory inputs, electrical
stimulation was applied to specific sites in the hindlimb and effects
on the nociceptive tail withdrawal reflex were monitored in the lightl
y anaesthetized rat. Stimulation was applied to previously defined sit
es in the hindlimb, meridian points femur-futu (ST-32), fengshi (GB-31
) and zusanli (ST-36). It consisted of a 4 Hz train of 2 ms square pul
ses given for 20 min at 20 X the threshold intensity required for musc
le twitch. Tail withdrawal was provoked by application of a noxious he
at stimulus applied to the tip of the tail. Results were expressed as
a percentage of the maximal possible inhibition which is achieved when
the post-treatment latency is 2 X the pre-treatment latency otherwise
known as the cut off. During stimulation, the latency of the withdraw
al increased to similar to 70% of the maximal possible inhibition. Fol
lowing stimulation, the inhibition persisted for > 1 h. Stimulation at
2 or 6 Hz elicited similar effects but stimulation at 8 Hz evoked inh
ibition during the stimulation only. Stimulation applied to sites away
from defined meridian points inhibited tail withdrawal during the sti
mulation; no post-stimulation effect was produced. In acutely transect
ed animals (less than or equal to 48 h), stimulation of meridian point
s elicited a small, brief increase in latency but during stimulation o
nly. At 7 and 14 days after spinal transection, this response during s
timulation was greater in magnitude and a brief post-stimulation incre
ase was also observed. The return of the of this latter effect was coi
ncident with the return of bladder function. These data suggest that h
igh intensity, low frequency electrical stimulation of hindlimb meridi
an points in the lightly anaesthetized rat produces both brief and per
sistent inhibitory effects on the nociceptive tail withdrawal reflex.
These effects appear to be elicited by different mechanisms. The persi
stent effect may represent a plastic change in central inhibitory mech
anisms. Data from spinal animals indicate a major participation of sup
raspinal structures but that spinal mechanisms are also capable of sus
taining both types of effect. (C) 1997 Elsevier Science B.V.