Intracisternal octreotide does not ameliorate orthodromic trigeminovascular nociception

Citation
Rha. Kemper et al., Intracisternal octreotide does not ameliorate orthodromic trigeminovascular nociception, CEPHALALGIA, 20(2), 2000, pp. 114-121
Citations number
51
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
CEPHALALGIA
ISSN journal
03331024 → ACNP
Volume
20
Issue
2
Year of publication
2000
Pages
114 - 121
Database
ISI
SICI code
0333-1024(200003)20:2<114:IODNAO>2.0.ZU;2-9
Abstract
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.