Mesolimbic dopaminergic decline after cannabinoid withdrawal.
M Diana, M Melis, A L Muntoni, G L Gessa
Proceedings of the National Academy of Sciences of the United States of America August 18, 1998 DOI: 10.1073/pnas.95.17.10269 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Rats |
| Interventions | Delta9-tetrahydrocannabinol (Delta9-THC) SR 141716A |
| Key findings | Chronic Delta9-THC administration reduced the activity of meso-accumbens dopamine neurons during both precipitated and spontaneous withdrawal. Delta9-THC re-administration restored neuronal activity in spontaneously withdrawn rats, while SR 141716A further decreased activity only in cannabinoid-treated rats, indicating reduced dopaminergic transmission during cannabinoid withdrawal. |
Abstract
The mesolimbic dopamine system has recently been implicated in the long-term aversive consequences of withdrawal from major drugs of abuse. In the present study we sought to determine whether mesolimbic dopamine neurons are involved in the neurobiologic mechanisms underlying withdrawal from chronic cannabinoid exposure. Rats were treated chronically with the major psychoactive ingredient of hashish and marijuana, Delta9-tetrahydrocannabinol (Delta9-THC). Administration of the cannabinoid antagonist SR 141716A precipitated an intense behavioral withdrawal syndrome, whereas abrupt Delta9-THC suspension failed to produce overt signs of abstinence. In contrast, both groups showed a reduction in dopamine cells activity as indicated by extracellular single unit recordings from antidromically identified meso-accumbens dopamine neurons. The administration of Delta9-THC to spontaneously withdrawn rats restored neuronal activity. Conversely, SR 141716A produced a further decrease of spontaneous activity in cannabinoid-treated although it was ineffective in control rats. These data indicate that withdrawal from chronic cannabinoid administration is associated with reduced dopaminergic transmission in the limbic system, similar to that observed with other addictive drugs; these changes in neuronal plasticity may play a role in drug craving and relapse into drug addiction.