G. Gerra et al., SEROTONERGIC FUNCTION AFTER (+ -)-3,4-METHYLENE-DIOXYMETHAMPHETAMINE (ECSTASY) IN HUMANS/, International clinical psychopharmacology, 13(1), 1998, pp. 1-9
(+/-)-3,4-Methylene-dioxymethamphetamine (MDMA, or 'Ecstasy') effects
on serotonin system function and behaviour in humans are unclear. Fift
een MDMA users, who did not have other drug dependencies or alcohol ab
use, and had not used other drugs for prolonged periods, and 15 contro
l individuals were included in a study to assess the biological and ps
ychological changes after chronic use of MDMA. Prolactin and cortisol
responses to D-fenfluramine challenge, clinical psychobehavioural chan
ges, personality characteristics, including mood, aggressiveness and t
emperamental aspects, were evaluated 3 weeks after MDMA discontinuatio
n. MDMA users had significantly reduced prolactin and cortisol respons
es in comparison with control individuals (p < 0.001 and p < 0.005, re
spectively). Dysphoria and mood changes were exhibited in seven indivi
duals, tiredness in five and sensation-seeking behaviour in twelve at
the clinical evaluation. Significantly higher scores were found in MDM
A individuals than in control individuals for Minnesota Multiphasic Pe
rsonality 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 unde
r the curve among MDMA users were negatively correlated with direct ag
gressiveness scores for Buss Durkee Hostility Inventory; a negative co
rrelation between prolactin responses and novelty-seeking scores was a
lso evidenced among MDMA users. These data suggest an association betw
een serotonin system impairment and MDMA use in humans; in interpretat
ion of these results, the possibility that serotonin deficit in MDMA i
ndividuals was partially related to a premorbid condition, in relation
ship with novelty-seeking behaviour and mood disorders, can not be exc
luded. (C) 1998 Rapid Science Ltd.