LAUSR

HIGHLIGHTSMicroinjection of LY2033298 (0.2 &mgr;g/side) into the NAcS blocked the expression of morphine‐induced behavioral sensitization.Tropicamide in the NAcS reversed the inhibitory effect of huperzine‐A on the expression of morphine‐induced behavioral sensitization.SKF38393 in the NAcS reversed the inhibitory effect of LY2033298 on the expression of morphine‐induced behavioral sensitization. ABSTRACT Repeated administration of morphine profoundly influences the dopaminergic and cholinergic systems in the nucleus accumbens [including the shell of the nucleus accumbens (NAcS)]. Further, dopamine release is regulated by the cholinergic system, especially the M4 receptor. Drug priming is one of the main factors that induces relapse in drug addiction. The present study first investigated how activation of the M4 receptor in the NAcS affects the expression of morphine‐induced behavioral sensitization, through the administration of an M4 agonist (LY2033298) and antagonist (tropicamide), as well as a combination of an acetylcholinesterase inhibitor and M4 antagonist (huperzine‐A + tropicamide). Additionally, the influence of a dopamine receptor agonist, in conjunction with an M4 agonist (i.e., SKF38393 + LY2033298), was also examined. Behavioral sensitization was established by exposure to 5 mg/kg morphine once every three days for a total of three exposures. The expression of behavioral sensitization was challenged by 5 mg/kg morphine. Results showed that (1) microinjection of the M4 receptor agonist LY2033298 (0.2 &mgr;g/side), but not the antagonist tropicamide (5, 10, or 20 &mgr;M/side) into the NAcS blocked the expression of behavioral sensitization; (2) tropicamide (20 &mgr;M/side) reversed the inhibition effect of huperzine‐A on this behavior; and (3) SKF38393 (1 &mgr;g/side) reversed the inhibitory effect of LY2033298 on the expression of morphine‐induced behavioral sensitization. These results suggest that the cholinergic M4 receptor in the NAcS plays an important role in the morphine‐induced expression of behavioral sensitization through the regulation of dopamine function in rats.