The development of chronic pain is associated with activity-dependent plast
ic changes in neuronal structures in the peripheral and central nervous sys
tem. In order to investigate the time-dependent processing of afferent noxi
ous stimuli in the spinal cord we employed the quantitative autoradiographi
c 2-deoxyglucose technique in a model of chronic monoarthritic pain in the
rat. Spinal metabolic activity was determined at various time-points (two,
four and 14 days) after the injection of complete Freund's adjuvant into th
e left tibiotarsal joint. In addition, the effect of acute noxious mechanic
al stimulation of the arthritic joint was investigated at 14 days of monoar
thritis. Local glucose utilization was determined in lumbar segments L-2-L-
5, ipsi- and contralateral to the inflamed hindpaw, and compared with salin
e-injected controls, in general, monoarthritic animals had bilaterally incr
eased metabolic activity in all laminae of the spinal cord. Detailing the t
ime-course showed that in rats with two days of monoarthritis metabolic act
ivity was significantly increased to a similar extent on both sides of all
spinal laminae. In contrast, at four days, glucose utilization in deep lami
nae of the dorsal horn (laminae V-VI), the central gray area (laminae X) an
d the ventral horn (laminae W-M) tended to return to control levels. At 14
days of monoarthritis, however, metabolic activity showed a further increas
e in all laminae of the spinal cord. This increase was more pronounced on t
he side ipsilateral to inflammation, reaching 65% above corresponding contr
ol levels in laminae V, VI. Animals with 14 days of monoarthritis which wer
e subjected to mechanical noxious stimulation of the arthritic joint displa
yed clear behavioral signs of acute pain. Although in this group metabolic
activity was above control levels, it was lower than in animals with 14 day
s of monoarthritis that were not additionally stimulated.
The data show not only a general increase of spinal cord metabolic activity
during the time-course of the development of a chronic pain state, but als
o show a region-specific non-linear time profile. This may reflect the comp
lexity of transducing and suppressive transmitter systems involved in the c
entral processing of ongoing pain. (C) 1999 IBRO. Published by Elsevier Sci
ence Ltd.