Sensitization to the prosocial effects of 3,4-methylenedioxymethamphetamine (MDMA).
Daniel W Curry, Laís F Berro, Andie R Belkoff, Agnieszka Sulima, Kenner C Rice, Leonard L Howell
Neuropharmacology June 2019 DOI: 10.1016/j.neuropharm.2019.03.017 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Animal experimental study Peer reviewed |
|---|---|
| Population | Mice |
| Interventions | MDMA MDL100907 |
| Dose | 7.8 mg/kg MDMA |
| Duration | Every other day for a week |
| Topics | MDMA |
| Keywords | 3,4-methylenedioxymethamphetamine 5-ht2a Sensitization Social interaction |
| Key findings | Repeated MDMA (7.8 mg/kg) paired with social interaction every other day for a week produced a sharp, progressive increase in social interaction in mice, a phenomenon the authors call social sensitization. This sensitization required a social context and 5-HT2A receptor activation: it did not develop with MDMA in isolation and was blocked by pretreatment with the 5-HT2A antagonist MDL100907, though MDL100907 did not reduce social interaction once sensitization had developed. |
Abstract
The recreational drug 3,4-methylenedioxymethamphetamine (MDMA) has well documented prosocial effects and is currently under clinical investigation as a treatment for patients with PTSD, autism, and other conditions. Early clinical trials have found that MDMA-assisted therapy may have robust long-lasting therapeutic effects, yet the mechanism by which acute treatments produce these long-term effects is unclear. Sensitization to certain behavioral drug effects is a common rodent model used to assess long-lasting neurobiological adaptations induced by acute drug treatments. Nine independent experiments were undertaken to investigate if and how mice sensitize to the prosocial effects of MDMA. When treated with 7.8 mg/kg MDMA and paired every other day for a week, MDMA-induced social interaction increased precipitously across treatment sessions. This previously unreported phenomenon was investigated and found to be heavily influenced by a social context and 5-HT2AR activation. Social sensitization did not appear to develop if mice were administered MDMA in isolation, and pretreatment with MDL100907, a selective 5-HT2AR antagonist, inhibited the development of social sensitization. However, when MDL100907 was administered to mice that had already been sensitized, it did not attenuate social interaction, suggesting that 5-HT2AR activity may be necessary for the development of social sensitization but not the expression of MDMA-induced social behavior. Additional investigation is warranted to further explore the phenomenon of social sensitization and to determine the underlying neurobiological mechanisms.