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The Journal of Neurophysiology Vol. 84 No. 2 August 2000, pp. 798-805
Copyright ©2000 by the American Physiological Society
Department of Anesthesiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205
Zhang, Jun-Ming,
Huiqing Li, and
Sorin J. Brull.
Perfusion of the Mechanically Compressed Lumbar Ganglion With
Lidocaine Reduces Mechanical Hyperalgesia and Allodynia in the
Rat. J. Neurophysiol. 84: 798-805, 2000. The
rat L5 dorsal root ganglion (DRG) was chronically
compressed by inserting a hollow perforated rod into the intervertebral foramen. The DRG was constantly perfused through the hollow rod with
either lidocaine or normal saline delivered by a subcutaneous osmotic
pump. Behavioral evidence for neuropathic pain after DRG compression
involved measuring the incidence of hindlimb withdrawals to both
punctate indentations of the hind paw with mechanical probes exerting
different bending forces (hyperalgesia) and to light stroking of the
hind paw with a cotton wisp (tactile allodynia). Behavioral results
showed that for saline-treated control rats: the withdrawal thresholds
for the ipsilateral and contralateral paws to mechanical stimuli
decreased significantly after surgery and the incidence of foot
withdrawal to light stroking significantly increased on both
ipsilateral and contralateral hind paws. Local perfusion of the
compressed DRG with 2% lidocaine for 7 days at a low flow-rate (1 µl/h), or for 1 day at a high flow-rate (8 µl/h) partially reduced
the decrease in the withdrawal thresholds on the ipsilateral foot but
did not affect the contralateral foot. The incidence of foot withdrawal
in response to light stroking with a cotton wisp decreased
significantly on the ipsilateral foot and was completely abolished on
the contralateral foot in the lidocaine treatment groups. This study
demonstrated that compression of the L5 DRG induced a
central pain syndrome that included bilateral mechanical hyperalgesia
and tactile allodynia. Results also suggest that a lidocaine block, or
a reduction in abnormal activity from the compressed ganglia to the
spinal cord, could partially reduce mechanical hyperalgesia and tactile allodynia.
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