Octreotide is a long-acting somatostatin analogue that has been effectively
used to treat migraine. Octreotide poorly penetrates the blood-brain barri
er, but has potential central target sites in the trigeminal nucleus caudal
is, which is the primary central relay station for trigeminal nociceptive i
nformation in the brain. We studied the effect of intracisternally applied
octreotide in a model of trigeminovascular stimulation in the unrestrained
rat using intracisternal capsaicin infusion to stimulate intracranial trige
minal nerves. Fos expression in the outer layers of the trigeminal nucleus
caudalis (TNC I-II) and behavioural analysis were used to measure the effec
ts of octreotide on capsaicin-induced trigeminovascular activation. Increas
es of head grooming and scratching behaviour are an indication of octreotid
e-induced trigeminal activation. However; octreotide did not alter the aver
age capsaicin-induced Fos expression in the TNC I-II and capsaicin sensitiv
e behaviours were not modified by octreotide pretreatment. This argues agai
nst a role for central (TNC I-II) somatostatin receptors in the processing
of the nociceptive trigeminovascular signals.