PMID- 16847678 OWN - NLM STAT- MEDLINE DCOM- 20070302 LR - 20181113 IS - 0033-3158 (Print) IS - 0033-3158 (Linking) VI - 189 IP - 4 DP - 2007 Jan TI - Neuroimaging research in human MDMA users: a review. PG - 539-56 AB - RATIONALE: Determining whether, under what circumstances, and to what extent 3,4-methylenedioxymethamphetamine (MDMA) exposure produces chronic changes in human brain function is a critical public health issue. MDMA is a widely used recreational drug commonly sold as "Ecstasy". Because findings from the animal literature have indicated that specific dosage regimens of MDMA can produce long-lasting alterations in serotonergic function, existing studies of MDMA effects in humans have examined brain serotonin (5-HT) transporters (5-HTT) and receptors or have examined brain structures or functions potentially affected by MDMA. OBJECTIVES: The objectives of this review are to provide a background for interpreting human MDMA neuroimaging research, to examine existing neuroimaging data regarding the rationale for and limitations to human MDMA research, and to provide suggestions for improving the design and interpretation of future neuroimaging approaches. RESULTS: Of the existing neuroimaging studies in human MDMA users, few experimental designs have been replicated across different research groups. Only investigations employing nuclear imaging methods to assay brain 5-HTT levels have been replicated across methods and research laboratories. These studies have found reduced levels of the 5-HTT in recently abstinent MDMA users with some evidence for normalization of 5-HTT levels with prolonged abstinence. However, the sensitivity of these methods is unknown. CONCLUSIONS: The current state of neuroimaging in human MDMA users does not permit conclusions regarding the long-term effects of MDMA exposure. Future study designs might benefit from improved sample homogeneity, increased length of MDMA abstinence, longitudinal study design, test-retest measures, serotonergic specificity, and multimodal approaches. FAU - Cowan, Ronald L AU - Cowan RL AD - Psychiatric Neuroimaging Program, Department of Psychiatry, Vanderbilt University Medical Center, 1500 21st Avenue South, Suite 3000, Nashville, TN 37212, USA. Ronald.L.Cowan@Vanderbilt.edu LA - eng GR - DA015137/DA/NIDA NIH HHS/United States GR - DA016617/DA/NIDA NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Review DEP - 20060718 PL - Germany TA - Psychopharmacology (Berl) JT - Psychopharmacology JID - 7608025 RN - 0 (Receptor, Serotonin, 5-HT2A) RN - 0 (SLC6A4 protein, human) RN - 0 (Serotonin Agents) RN - 0 (Serotonin Plasma Membrane Transport Proteins) RN - 30KYC7MIAI (Aspartic Acid) RN - 333DO1RDJY (Serotonin) RN - 4L6452S749 (Inositol) RN - 997-55-7 (N-acetylaspartate) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Amphetamine-Related Disorders/*diagnostic imaging/etiology/metabolism/physiopathology/psychology MH - Aspartic Acid/analogs & derivatives/metabolism MH - Attention/drug effects MH - Biomedical Research/methods MH - Brain/*diagnostic imaging/drug effects/metabolism/physiopathology MH - Cerebrovascular Circulation MH - Humans MH - Inositol/metabolism MH - Memory/drug effects MH - N-Methyl-3,4-methylenedioxyamphetamine/*adverse effects MH - *Positron-Emission Tomography/methods MH - Receptor, Serotonin, 5-HT2A/metabolism MH - Reproducibility of Results MH - Research Design MH - Serotonin/metabolism MH - Serotonin Agents/*adverse effects MH - Serotonin Plasma Membrane Transport Proteins/metabolism MH - *Tomography, Emission-Computed, Single-Photon/methods RF - 115 EDAT- 2006/07/19 09:00 MHDA- 2007/03/03 09:00 CRDT- 2006/07/19 09:00 PHST- 2005/06/02 00:00 [received] PHST- 2006/06/01 00:00 [accepted] PHST- 2006/07/19 09:00 [pubmed] PHST- 2007/03/03 09:00 [medline] PHST- 2006/07/19 09:00 [entrez] AID - 10.1007/s00213-006-0467-3 [doi] PST - ppublish SO - Psychopharmacology (Berl). 2007 Jan;189(4):539-56. doi: 10.1007/s00213-006-0467-3. Epub 2006 Jul 18.