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Serotonergic function after (±)3,4-methylene-dioxymethamphetarnine (‘Ecstasy’) in humans

Gilberto Gerra, A. Zaimovic, Giuliano Giucastro, D. Maestri, C. Monica, Rodrigo Flores Sartori, R. Caccavari, R Delsignore

International Clinical Psychopharmacology January 1, 1998 DOI: 10.1097/00004850-199801000-00001 via OpenAlex

Summary

AI-generated from the abstract

Chronic use of MDMA (Ecstasy) is associated with impaired serotonin system function and behavioral changes. Fifteen MDMA users without other drug dependencies showed significantly reduced prolactin and cortisol responses to a D-fenfluramine challenge compared to 15 control individuals, indicating serotonergic dysfunction. Clinically, users exhibited dysphoria, mood changes, tiredness, and sensation-seeking behavior. They scored higher on depression, hostility, and novelty-seeking measures. Prolactin responses negatively correlated with direct aggressiveness and novelty-seeking scores. The findings suggest a link between MDMA use and serotonin impairment, though a premorbid condition contributing to these differences cannot be ruled out.

Study at a glance

Characteristics Case-control study Peer reviewed
Sample size 30
Population MDMA users and control individuals without other drug dependencies or alcohol abuse
Intervention D-fenfluramine challenge
Duration 3 weeks after MDMA discontinuation
Topics MDMA Serotonin
Keywords Fenfluramine Novelty seeking Clinical psychology
Citations 145
Key finding Chronic MDMA users had significantly reduced prolactin and cortisol responses to D-fenfluramine challenge, indicating serotonin system impairment, along with elevated depression, hostility, and novelty-seeking scores.

Abstract

(+/-)3,4-Methylene-dioxymethamphetamine (MDMA, or 'Ecstasy') effects on serotonin system function and behaviour in humans are unclear. Fifteen MDMA users, who did not have other drug dependencies or alcohol abuse, and had not used other drugs for prolonged periods, and 15 control individuals were included in a study to assess the biological and psychological changes after chronic use of MDMA. Prolactin and cortisol responses to D-fenfluramine challenge, clinical psychobehavioural changes, personality characteristics, including mood, aggressiveness and temperamental aspects, were evaluated 3 weeks after MDMA discontinuation. MDMA users had significantly reduced prolactin and cortisol responses in comparison with control individuals (p < 0.001 and p < 0.005, respectively). Dysphoria and mood changes were exhibited in seven individuals, tiredness in five and sensation-seeking behaviour in twelve at the clinical evaluation. Significantly higher scores were found in MDMA individuals than in control individuals for Minnesota Multiphasic Personality Inventory subscale for Depression, for Buss Durkee Hostility Inventory direct and guilt subscales, for Hamilton Depression Rating Scale and for novelty-seeking Tridimensional Personality Questionnaire subscale. Prolactin responses to D-fenfluramine stimulation area under the curve among MDMA users were negatively correlated with direct aggressiveness scores for Buss Durkee Hostility Inventory; a negative correlation between prolactin responses and novelty-seeking scores was also evidenced among MDMA users. These data suggest an association between serotonin system impairment and MDMA use in humans; in interpretation of these results, the possibility that serotonin deficit in MDMA individuals was partially related to a premorbid condition, in relationship with novelty-seeking behaviour and mood disorders, can not be excluded.

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