Role of Serotonin via 5-HT2B Receptors in the Reinforcing Effects of MDMA in Mice
Stéphane Doly, Jesus Bertran‐gonzalez, Jacques Callebert, Alexandra Bruneau, Sophie M. Banas, Arnauld Belmer, Katia Boutourlinsky, Denis Hervé, Jean‐marie Launay, Luc Maroteaux
PLoS ONE November 20, 2009 DOI: 10.1371/journal.pone.0007952 via OpenAlex
Summary
AI-generated from the abstractThe drug MDMA (ecstasy) produces its rewarding effects by causing the release of serotonin and dopamine in brain regions linked to reward. This study shows that the 5-HT(2B) receptor, a type of serotonin receptor, is essential for MDMA's reinforcing properties. Mice lacking the 5-HT(2B) receptor did not develop a preference for the location where they received MDMA (10 mg/kg) nor did they show behavioral sensitization. Blocking this receptor with an antagonist also prevented these effects in normal mice. However, at a higher dose (30 mg/kg), MDMA's effects were independent of serotonin and the 5-HT(2B) receptor, relying instead on dopamine. These findings highlight the dose-dependent role of serotonin-dopamine interactions in MDMA's addictive potential.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Mice (5-HT(2B) knockout and wild type) |
| Intervention | MDMA |
| Dose | 10 mg/kg, 30 mg/kg |
| Topics | MDMA Serotonin |
| Keywords | Pharmacology 5-HT Receptor Nucleus accumbens |
| Citations | 80 |
| Key finding | The 5-HT(2B) receptor is required for the reinforcing properties of low-dose MDMA, but high-dose MDMA produces dopamine-dependent effects independent of this receptor. |
Abstract
The amphetamine derivative 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) reverses dopamine and serotonin transporters to produce efflux of dopamine and serotonin, respectively, in regions of the brain that have been implicated in reward. However, the role of serotonin/dopamine interactions in the behavioral effects of MDMA remains unclear. We previously showed that MDMA-induced locomotion, serotonin and dopamine release are 5-HT(2B) receptor-dependent. The aim of the present study was to determine the contribution of serotonin and 5-HT(2B) receptors to the reinforcing properties of MDMA.We show here that 5-HT(2B) (-/-) mice do not exhibit behavioral sensitization or conditioned place preference following MDMA (10 mg/kg) injections. In addition, MDMA-induced reinstatement of conditioned place preference after extinction and locomotor sensitization development are each abolished by a 5-HT(2B) receptor antagonist (RS127445) in wild type mice. Accordingly, MDMA-induced dopamine D1 receptor-dependent phosphorylation of extracellular regulated kinase in nucleus accumbens is abolished in mice lacking functional 5-HT(2B) receptors. Nevertheless, high doses (30 mg/kg) of MDMA induce dopamine-dependent but serotonin and 5-HT(2B) receptor-independent behavioral effects.These results underpin the importance of 5-HT(2B) receptors in the reinforcing properties of MDMA and illustrate the importance of dose-dependent effects of MDMA on serotonin/dopamine interactions.