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| Content Provider | PubMed Central |
|---|---|
| Author | Matthew, Walentiny D. Gamage, Thomas F. Warner, Jonathan A. Nguyen, Thanh K. Grainger, Darren B. Wiley, Jenny L. Vann, Robert E. |
| Copyright Year | 2010 |
| Abstract | The endogenous cannabinoid system has been noted for its therapeutic potential, as well as the psychoactivity of cannabinoids such as Δ9-tetrahydrocannabinol (THC). However, less is known about the psychoactivity of anandamide (AEA), an endocannabinoid ligand. Thus, the goals of this study were to establish AEA as a discriminative stimulus in transgenic mice lacking fatty acid amide hydrolase (i.e., FAAH −/− mice unable to rapidly metabolize AEA), evaluate whether THC or oleamide, a fatty acid amide, produced AEA-like responding, and assess for CB1 mediation of AEA’s discriminative stimulus. Mice readily discriminated between 6 mg/kg AEA and vehicle in a two-lever drug discrimination task. AEA dose-dependently generalized to itself. THC elicited full AEA-like responding, whereas oleamide failed to substitute. The CB1 antagonist rimonabant attenuated AEA- and THC-induced AEA-appropriate responding, demonstrating CB1 mediation of AEA’s discriminative stimulus. These findings suggest that, in the absence of FAAH, AEA produces intoxication comparable to THC, and consequently to marijuana. |
| Related Links | http://dx.doi.org/10.1016/j.ejphar.2011.01.056 |
| Ending Page | 67 |
| Page Count | 5 |
| Starting Page | 63 |
| File Format | |
| ISSN | 00142999 |
| e-ISSN | 18790712 |
| Journal | European journal of pharmacology |
| Issue Number | 1-3 |
| Volume Number | 656 |
| Language | English |
| Publisher Date | 2011-04-01 |
| Access Restriction | Open |
| Subject Keyword | Pharmacology Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Pharmacology |
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