WE studied pronociceptin gene expression following limbic seizures. Norther
n blot analysis revealed increased pronociceptin mRNA levels in the thalamu
s (but not in the hippocampus) 3-24h after kainate administration, with max
imal effect (2-fold increase over basal levels) reached at 6h. No variation
in pronociceptin mRNA levels was observed 1-6h after a stimulus-evoked kin
dled seizure. Carrageenan failed to affect pronociceptin gene expression in
the thalamus, indicating that pain and/or acute stress do not account for
kainate effects. In situ hybridization revealed that kainate evokes a drama
tic (4-fold) increase in pronociceptin mRNA levels over the thalamic reticu
lar nucleus. Kindled seizures evoked only a small, nonsignificant increase
in pronociceptin gene expression over the dentate gyrus of the hippocampus.
(C) 1999 Lippincott Williams & Wilkins.