S. Yabuki et al., EFFECTS OF LIDOCAINE ON NUCLEUS PULPOSUS-INDUCED NERVE ROOT INJURY - A NEUROPHYSIOLOGIC AND HISTOLOGIC-STUDY OF THE PIG CAUDA-EQUINA, Spine (Philadelphia, Pa. 1976), 23(22), 1998, pp. 2383-2389
Study Design. Application of autologous nucleus pulposus on nerve root
s and treatment with local application of lidocaine in the pig. Object
ives. Studies of the effects of lidocaine on nucleus pulposus-exposed
nerve roots. Summary of Background Data. Nerve root infiltration may i
mprove radicular symptoms beyond the pharmacologic duration local anes
thetics, but the mechanisms for this effect are not known. Methods. Nu
cleus pulposus was harvested from a lumbar disc and placed onto the sa
crococcygeal cauda equina in pigs. In Series 1, early lidocaine treatm
ent of nucleus pulposus-induced nerve root injury, pigs received 2% li
docaine (n = 5) or saline (n = 5) before and after surgery. Nerve cond
uction velocity and histologic appearance were studied after 3 days. I
n Series 2, delayed lidocaine treatment of nucleus pulposus-induced ne
rve root injury, after 7 days 2% lidocaine was administered epidurally
to nucleus pulposus-exposed (n = 4) and -nonexposed (n = 4) nerve roo
ts. Nerve conduction velocity, muscle action potentials, and histologi
c appearance were assessed. Results. In Series 1, early treatment with
lidocaine limited the reduction in nerve conduction velocity. The epi
dural inflammation was less in lidocaine treated animals. In Series 2,
nerve conduction velocity was lower in nucleus pulposus-exposed anima
ls than in nonexposed animals. The initial reduction of nerve conducti
on velocity and muscle action potential was similar between the groups
, but the recovery of muscle action potential was slower and less comp
lete in nucleus pulposus-exposed nerve roots. There was minimal histol
ogic nerve injury in both series and in both protocols. Conclusions. E
arly treatment with lidocaine may reduce nucleus pulposus-induced nerv
e root injury. Lidocaine induced a delayed recovery in nerve roots exp
osed to nucleus pulposus. Further studies are needed to clarify the th
erapeutic effects of nerve root infiltration and the pathophysiology o
f nucleus pulposus-induced nerve root injury.