FLUNARIZINE ANALGESIA IS MEDIATED BY MU-OPIOID RECEPTORS

Citation
R. Weizman et al., FLUNARIZINE ANALGESIA IS MEDIATED BY MU-OPIOID RECEPTORS, Physiology & behavior, 62(5), 1997, pp. 1193-1195
Citations number
7
Categorie Soggetti
Psychology, Biological","Behavioral Sciences",Physiology
Journal title
ISSN journal
00319384
Volume
62
Issue
5
Year of publication
1997
Pages
1193 - 1195
Database
ISI
SICI code
0031-9384(1997)62:5<1193:FAIMBM>2.0.ZU;2-Z
Abstract
We evaluated the opioid antinociceptive mechanism of the calcium chann el blocker flunarizine. Flunarizine produced a dose-dependent, analges ia in the hot plate test which was antagonized by general (naloxone) a nd mu [beta-fualtrexamine (beta-FNA)]-opioid antagonists, indicating a role for CL receptors in flunarizine analgesia. Naltrindole (delta(1) antagonist) did not affect flunarizine analgesia. A fixed subthreshol d dose of flunarizine augmented mu (morphine) analgesia and blocked de lta(1) [enkephalin, [D-Pen(2,5)] (DPDPE)] analgesia. Apparently, fluna rizine has mu agonistic activity and delta(1) antagonist or mixed agon istic-antagonistic activity. (C) 1997 Elsevier Science Inc.