Psychological and physiological effects of MDMA ("ecstasy") after pretreatment with the 5-HT2 antagonist ketanserin in healthy humans

被引:178
作者
Liechti, ME [1 ]
Saur, MR [1 ]
Gamma, A [1 ]
Hell, D [1 ]
Vollenweider, FX [1 ]
机构
[1] Univ Zurich, Hosp Psychiat, Res Unit, CH-8029 Zurich, Switzerland
关键词
MDMA; ecstasy; ketanserin; serotonin;
D O I
10.1016/S0893-133X(00)00126-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
MDMA (3,4-methylenedioxymethamphetamine, "Ecstasy") mainly releases serotonin and dopamine. In animals, pretreatment with 5-HT2 antagonists has been shown to attenuate neurochemical and behavioral effects of MDMA. In humans, the role of 5-HT2 receptors in the action of MDMA has not been studied. We investigated the effect of pretreatment with the 5-HT2A/C antagonist ketanserin (50 mg p.o.) on subjective responses to MDMA (1.5 mg/kg p.o.) in 14 healthy volunteers using a double-blind placebo-controlled within-subject design. Subjective effects were rated by psychometric rating scales. Physiological effects measured were blood pressure, heart rate, and body temperature. Adverse effects were assessed during the sessions, and after one and three days. Ketanserin attenuated MDMA-induced perceptual changes, emotional excitation, and acute adverse responses but had little effect on MDMA-induced positive mood, well-being, extroversion, and short-term sequence. Body temperature was lower under MDMA plus ketanserin compared to MDMA alone. The results suggest a contributing role for 5-HT2 receptors in the action of MDMA in humans. (C) 2000 American College of Neuropsychopharmacology. Published by Elsevier Science Inc.
引用
收藏
页码:396 / 404
页数:9
相关论文
共 40 条
[31]   EFFECTS OF INTRAVENOUS COCAINE ARE PARTIALLY ATTENUATED BY HALOPERIDOL [J].
SHERER, MA ;
KUMOR, KM ;
JAFFE, JH .
PSYCHIATRY RESEARCH, 1989, 27 (02) :117-125
[32]  
Spielberger CD, 1970, The State Trait Anxiety Inventory (Self Evaluation Questionnaire)
[33]  
TITELER M, 1988, PSYCHOPHARMACOLOGY, V94, P213
[34]   Relationship between subjective effects of cocaine and dopamine transporter occupancy [J].
Volkow, ND ;
Wang, GJ ;
Fischman, MW ;
Foltin, RW ;
Fowler, JS ;
Abumrad, NN ;
Vitkun, S ;
Logan, J ;
Gatley, SJ ;
Pappas, N ;
Hitzemann, R ;
Shea, CE .
NATURE, 1997, 386 (6627) :827-830
[35]   Effects of high amphetamine dose on mood and cerebral glucose metabolism in normal volunteers using positron emission tomography (PET) [J].
Vollenweider, FX ;
Maguire, RP ;
Leenders, KL ;
Mathys, K ;
Angst, J .
PSYCHIATRY RESEARCH-NEUROIMAGING, 1998, 83 (03) :149-162
[36]  
Vollenweider FX, 1999, NEUROPSYCHOPHARMACOL, V21, P598
[37]   Psychological and cardiovascular effects and short-term sequelae of MDMA ("Ecstasy") in MDMA-naive healthy volunteers [J].
Vollenweider, FX ;
Gamma, AG ;
Liechti, M ;
Huber, T .
NEUROPSYCHOPHARMACOLOGY, 1998, 19 (04) :241-251
[38]   Psilocybin induces schizophrenia-like psychosis in humans via a serotonin-2 agonist action [J].
Vollenweider, FX ;
Vollenweider-Scherpenhuyzen, MFI ;
Bäbler, A ;
Vogel, H ;
Hell, D .
NEUROREPORT, 1998, 9 (17) :3897-3902
[39]   THE ACUTE EFFECTS OF METHYLENEDIOXYMETHAMPHETAMINE ON DOPAMINE RELEASE IN THE AWAKE-BEHAVING RAT [J].
YAMAMOTO, BK ;
SPANOS, LJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 148 (02) :195-203
[40]  
ZERSSEN DV, 1976, BESCHWERDEN LISTE BL