J. Buritova et al., INVOLVEMENT OF THE SPINOPARABRACHIAL PATHWAY IN INFLAMMATORY NOCICEPTIVE PROCESSES - A C-FOS PROTEIN STUDY IN THE AWAKE RAT, Journal of comparative neurology, 397(1), 1998, pp. 10-28
The effect of graded inflammatory stimuli (intraplantar-carrageenan, 0
.2, 1, and 6 mg/150 mu l) on paw edema and c-Fos protein expression at
two levels of the spinoparabrachial pathway the spinal cord and parab
rachial area (PB), were studied. The present study, in awake rats, is
an extension of previous study (Bester et al. [1997] J. Comp. Neurol.
383:339-458) which evaluated, in anesthetized rats, the effect of grad
ed cutaneous heat stimulation on c-Fos-expression at the same levels.
At the spinal level, the c-Fos-protein-like-immunoreactive (c-Fos-LI)
neurons were located primarily in superficial laminae ipsilateral to i
ntraplantar carrageenan. The number of c-Fos-LI neurons increased dose
dependently (r = 0.973, n = 24) for carrageenan, from a number close
to zero for the saline injection. At the PB level, c-Fos was predomina
ntly expressed contralateral to intraplantar carrageenan, c-Fos-LI neu
rons were located primarily around the pontomesencephalic junction in
(i) a restricted pontine area, centered in the lateral crescent, and i
ncluding an adjacent part of the outer portion of the external lateral
subnucleus, and (ii) the mesencephalic superior lateral subnuclei. Th
e number of c-Fos-LI neurons in the PB area was correlated with that i
n the superficial laminae (r = 0.935, n = 24) and with the paw edema (
r = 0.931, n = 24). No significant changes in c-Fos expression were ob
served in the nucleus of the solitary tract and ventrolateral medulla.
The close correlation between c-Fos expression at both the spinal and
PB levels and inflammatory edema provides further evidence for the in
volvement of spinoparabrachial pathway in inflammatory nociceptive pro
cesses. The present results are congruent with the existence of electr
ophysiologically demonstrated spinoparabrachio-amygdaloid and -hypotha
lamic nociceptive pathways. (C) 1998 Wiley-Liss, Inc.