Altered dopamine D1 and D2 receptor mRNA expression in mesencephalon from mice exposed to repeated treatments with methamphetamine and cannabinoid CB1 agonist methanandamide
Language English Country Sweden Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22936253
PII: NEL330412A11
Knihovny.cz E-resources
- MeSH
- Behavior, Animal drug effects MeSH
- Dopamine Agents pharmacology MeSH
- Receptor Cross-Talk drug effects MeSH
- Arachidonic Acids pharmacology MeSH
- Drug Interactions MeSH
- RNA, Messenger analysis MeSH
- Methamphetamine pharmacology MeSH
- Mesencephalon drug effects metabolism MeSH
- Mice, Inbred ICR MeSH
- Mice MeSH
- Random Allocation MeSH
- Motor Activity drug effects MeSH
- Receptor, Cannabinoid, CB1 agonists MeSH
- Receptors, Dopamine D1 drug effects genetics metabolism MeSH
- Receptors, Dopamine D2 drug effects genetics metabolism MeSH
- Drug Administration Schedule MeSH
- Central Nervous System Sensitization drug effects MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Dopamine Agents MeSH
- Arachidonic Acids MeSH
- RNA, Messenger MeSH
- Methamphetamine MeSH
- methanandamide MeSH Browser
- Receptor, Cannabinoid, CB1 MeSH
- Receptors, Dopamine D1 MeSH
- Receptors, Dopamine D2 MeSH
OBJECTIVES: In our previous studies we found that both acute administration of CB1 receptor agonist methanandamide and repeated methanandamide pre-treatment prior to methamphetamine challenge dose elicited increase in the CB1 receptor mRNA expression in the mouse mesencephalon. As a reciprocal cross-talk is reported between the cannabinoid CB1 and dopamine receptors, that are highly co-localized on brain neurones, we targeted possible changes in relative expression of dopamine D1 and D2 receptor mRNA in mesencephalon in mice sensitized by repeated treatments to methamphetamine stimulatory effects and cross-sensitized to methamphetamine by cannabinoid CB1 receptor agonist methanandamide pre-treatment. METHODS: To confirm development of behavioural sensitization or cross-sensitization, respectively, we observed changes in locomotion using the open field test. Mice were treated repeatedly with either methamphetamine or methamphetamine after repeated pre-treatment with methanandamide. After each measurement of locomotion one third of animals were sacrificed and the brain was stored. RNA was isolated from the midbrain and used for reverse transcription and subsequent real-time PCR. RESULTS AND CONCLUSION: As in many of our earlier studies with the same dosage regimen we found in the behavioural part both development of sensitization to methamphetamine stimulatory effects after repeated treatment and cross-sensitization to them by pre-treatment with cannabinoid receptor CB1 agonist methanandamide. Real-time PCR analyses showed an increase in D1 receptor mRNA expression after the first dose of methamphetamine (that persisted also after the last dose of methamphetamine) and after the first dose of methanandamide (which also persisted after the methamphetamine challenge dose). In opposite a significant decrease in D2 receptor mRNA expression both after the first dose of methamphetamine and methanandamide (that persisted also after the methamphetamine challenge doses) was registered. Thus, our results suggest that both methamphetmine and methanandamide treatment can provoke changes in dopamine receptor density in mouse mesenpcephalon, the increase in D1 and decrease in D2 receptor subtypes.