Large receptor reserve for cannabinoid actions in the central nervous system

The receptor occupancy required to produce cannabinoid effects in the centr al nervous system was determined in both a neurochemical and a behavioral a ssay for cannabinoid actions. In the neurochemical experiments, performed o n superfused rat hippocampal slices, electrically evoked [H-3]acetylcholine release was inhibited by the cannabinoid agonist, WIN 55212 to 2 with an E C50 of 0.005 mu M and maximum effect of 79%. In parallel experiments examin ing binding of the radiolabeled CB1 antagonist [I-131]AM 281 {N-(morpholin- 4-yl)-5-(4-[I-131]iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3 -carboxamide} to living hippocampal slices, WIN 55212 to 2 inhibited [I-131 ]AM 281 binding with an EC50 of 1.3 mu M. From these two sets of data it wa s determined that 50% of maximal inhibition of [H-3]acetylcholine release i n hippocampal slices occurs at a receptor occupancy of only 0.13% and 95% o f maximal inhibition at a receptor occupancy of 7.5%, suggesting the presen ce of a receptor reserve that is large compared with other G protein-couple d receptor systems in the central nervous system. In behavioral experiments , WIN 55212 to 2 inhibited spontaneous locomotor activity in mice with an E D50 of 0.3 mg/kg, i.v.. In in vivo binding experiments using [I-131]AM 281, WIN 55212 to 2 failed to produce significant inhibition of radiotracer bin ding in the mouse brains, except at very high doses (10 mg/kg or greater, i .v.). By contrast, the CB1 antagonist SR 141716A(10 mg/kg, i.p.), completel y abolished specific [I-131]AM 281 binding. These experiments suggest that behavioral effects of cannabinoids, like neurochemical effects, are produce d at very low receptor occupancy.