Sensitization to the prosocial effects of 3,4-methylenedioxymethamphetamine (MDMA)

The rodent model study explored the sensitization to the prosocial effects of MDMA (7.8 mg/kg). The results found that social interaction increased sharply and substantially under the MDMA effects across treatment sessions and the mechanism was found to be heavily influenced by a social context and 5-HT2AR activation, which belongs to the serotonin receptor family. The study concluded that 5-HT2AR activity may play a significant role in the development of social sensitization but not the expression in social behavior under the MDMA effects.

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.

Authors: Daniel W. Curry, Laís F. Berro, Andie R. Belkoff, Agnieszka Sulima, Kenner C. Rice & Leonard L. Howell

Study details

Compounds studied
MDMA

Topics studied
Anxiety

Study characteristics
Animal Study