E. Acquas et al., Cannabinoid CB1 receptor agonists increase rat cortical and hippocampal acetylcholine release in vivo, EUR J PHARM, 401(2), 2000, pp. 179-185
Intravenous administration of the cannabinoid CB, receptor agonists (R-(+)-
[2,3-Dihydro-5-methyl-3[morpholinyl)me pyrrolo[1,2,3-de]-1,4-benzoxazinyl]-
(1-naphthalenyl)methanone mesylate), WIN 55,212-2 (10, 37.5, 75 and 150 mu
g/kg), and ((6aR)trans-3-(1, 1-Dimethylheptyl)-6a,7,10,10a-tetrahydro-1-hyd
roxy-6,6-dimethyl-6H-dibenzo[b,d]pyran-9-methanol), HU 210 (1 and 4 mu g/kg
) dose-dependently increased acetylcholine release in dialysates from the p
refrontal cortex and the hippocampus of freely moving rats. Administration
of the cannabinoid receptor antagonist {N-(piperidin-1-yl)-5-(4-chloropheny
l)-1-(2,3-dichlorophenyl)-3-methyl-1H-pyrazole-3carboxamide}HCl, SR 141716A
, at a dose that per se did not affect basal acetylcholine release (2.5 mu
g/kg), prevented the increase of acetylcholine release by WIN 55,212-2 (150
mu g/kg i.v.) or by HU 210 (4 mu g/kg i.v.) in both areas. These data demo
nstrate that, at low i.v. doses, the synthetic cannabinoid CB1 receptor ago
nists, WIN 55,212-2 and HU 210 stimulate cortical and hippocampal acetylcho
line release. (C) 2000 Elsevier Science B.V. All rights reserved.