No Evidence that MDMA-Induced Enhancement of Emotional Empathy Is Related to Peripheral Oxytocin Levels or 5-HT1a Receptor Activation

The present study aimed at investigating the effect of MDMA on measures of empathy and social interaction, and the roles of oxytocin and the 5-HT1A receptor in these effects. The design was placebo-controlled within-subject with 4 treatment conditions: MDMA (75 mg), with or without pindolol (20 mg),...

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Published inPloS one Vol. 9; no. 6; p. e100719
Main Authors Kuypers, Kim P. C., de la Torre, Rafael, Farre, Magi, Yubero-Lahoz, Samanta, Dziobek, Isabel, Van den Bos, Wouter, Ramaekers, Johannes G.
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 27.06.2014
Public Library of Science (PLoS)
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Summary:The present study aimed at investigating the effect of MDMA on measures of empathy and social interaction, and the roles of oxytocin and the 5-HT1A receptor in these effects. The design was placebo-controlled within-subject with 4 treatment conditions: MDMA (75 mg), with or without pindolol (20 mg), oxytocin nasal spray (40 IU+16 IU) or placebo. Participants were 20 healthy poly-drug MDMA users, aged between 18-26 years. Cognitive and emotional empathy were assessed by means of the Reading the Mind in the Eyes Test and the Multifaceted Empathy Test. Social interaction, defined as trust and reciprocity, was assessed by means of a Trust Game and a Social Ball Tossing Game. Results showed that MDMA selectively affected emotional empathy and left cognitive empathy, trust and reciprocity unaffected. When combined with pindolol, these effects remained unchanged. Oxytocin did not affect measures of empathy and social interaction. Changes in emotional empathy were not related to oxytocin plasma levels. It was concluded that MDMA (75 mg) selectively enhances emotional empathy in humans. While the underlying neurobiological mechanism is still unknown, it is suggested that peripheral oxytocin does not seem to be the main actor in this; potential candidates are the serotonin 2A and the vasopressin 1A receptors. Trial registration: MDMA & PSB NTR 2636.
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Competing Interests: RdlT confirmed that he is an Academic Editor of PLOS ONE. This does not alter the authors' adherence to PLOS ONE Editorial policies and criteria.
Conceived and designed the experiments: KK JR. Performed the experiments: KK. Analyzed the data: KK JR SY-L RdlT MF. Contributed reagents/materials/analysis tools: KK RdlT MF SY-L ID WvdB JR. Contributed to the writing of the manuscript: KK RdlT MF SY-L ID WvdB JR.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0100719