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The relative balance between acetylcholine and dopamine systems in the nucleus accumbens shell mediates morphine-induced behavioral sensitization in rat
Joint Event on Global Summit on Traditional & Restorative Medicine & 10th World Congress on Neuropharmacology
Behavioral sensitization reflects long-term adaptive changes in the central nervous
system induced by repeated exposure to drugs of abuse and the process of pathological
motivation for drugs or drug-wanting. Previous studies have demonstrated that repeated
administration of morphine increased dopamine but decreased acetylcholine in the nucleus
accumbens, which included the shell of the nucleus accumbens (NAcS). The present study
investigated the effect of balance between the cholinergic and dopaminergic systems in
the NAcS on morphine-induced behavioral sensitization. Behavioral sensitization was
established by exposure to 5 mg/kg morphine once every three days for a total of three
exposures. Expression of behavioral sensitization was challenged by 5 mg/kg morphine.
The results showed that: The acetylcholinesterase inhibitor huperzine-A (0.5 μg/side)
microinjected into the NAcS blocked initiation and expression of morphine-induced
behavioral sensitization, which were reversed by the dopamine D1 receptor agonist
SKF38393; The muscarinic receptor antagonist scopolamine (10.8 μg/side) had no effect
on morphine-induced behavioral sensitization; We further investigated the role of the
M4 receptor in expression of morphine-induced behavioral sensitization because the
expression stage is more related to relapse. Microinjection of the M4 receptor agonist
LY2033298 (0.2 μg/side), but not the antagonist tropicamide (5, 10, or 20 μM/side),
into the NAcS blocked expression of behavioral sensitization; Furthermore, tropicamide
(20 μM/side) reversed the inhibition effect of huperzine-A; and SKF38393 (1 μg/
side) reversed the inhibitory effect of LY2033298 on expression of morphine-induced
behavioral sensitization. Our findings suggest that the balance between dopamine and
acetylcholine in the NAcS modulates morphine-induced behavioral sensitization, which
can be regulated by the M4 receptor.
Biography
Xinwang Li has completed his PhD from Capital Normal University. He is a Professor of the Physiological Psychology in Capital Normal University, China. He has published more than 30 papers in reputed journals and Physiological Psychology (teaching material). He has been serving as the Deputy Chairman of the Chinese Committee of Physiological Psychology and an Editorial Board Member of Advances in Psychological Science.