PMID- 21603895 OWN - NLM STAT- MEDLINE DCOM- 20120213 LR - 20211020 IS - 1432-2072 (Electronic) IS - 0033-3158 (Linking) VI - 217 IP - 4 DP - 2011 Oct TI - Altered pain responses in abstinent (+/-)3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") users. PG - 475-84 LID - 10.1007/s00213-011-2303-7 [doi] AB - RATIONALE: (+/-)3,4-Methylenedioxymethamphetamine (MDMA) is a popular recreational drug that has potential to damage brain serotonin (5-HT) neurons in humans. Brain 5-HT neurons play a role in pain modulation, yet little is known about long-term effects of MDMA on pain function. Notably, MDMA users have been shown to have altered sleep, a phenomenon that can lead to altered pain modulation. OBJECTIVES: This study sought to assess pain processing in MDMA users using objective methods, and explore potential relationships between pain processing and sleep indices. METHODS: Forty-two abstinent MDMA users and 43 age-matched controls participated in a 5-day inpatient study. Outcome measures included standardized measures of pain, sleep polysomnograms, and power spectral measures of the sleep EEG. When differences in psychophysiological measures of pain were found, the relationship between pain and sleep measures was explored. RESULTS: MDMA users demonstrated lower pressure pain thresholds, increased cold pain ratings, increased pain ratings during testing of diffuse noxious inhibitory control, and decreased Stage 2 sleep. Numerous significant relationships between sleep and pain measures were identified, but differences in sleep between the two groups were not found to mediate altered pain perception in MDMA users. CONCLUSIONS: Abstinent MDMA users have altered pain perception and sleep architecture. Although pain and sleep outcomes were related, differences in sleep architecture in MDMA users did not mediate altered pain responses. It remains to be determined whether alterations in pain perception in MDMA users are secondary to neurotoxicity of 5-HT-mediated pain pathways or alterations in other brain processes that modulate pain perception. FAU - McCann, Una D AU - McCann UD AD - Department of Psychiatry and Behavioral Sciences, The Johns Hopkins University School of Medicine, 5501 Hopkins Bayview Circle, Room 5B71c, Baltimore, MD 21224, USA. umccann@jhmi.edu FAU - Edwards, Robert R AU - Edwards RR FAU - Smith, Michael T AU - Smith MT FAU - Kelley, Kristen AU - Kelley K FAU - Wilson, Michael AU - Wilson M FAU - Sgambati, Francis AU - Sgambati F FAU - Ricaurte, George AU - Ricaurte G LA - eng GR - R01 DA05938/DA/NIDA NIH HHS/United States GR - R01 DA16563/DA/NIDA NIH HHS/United States PT - Clinical Trial PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20110521 PL - Germany TA - Psychopharmacology (Berl) JT - Psychopharmacology JID - 7608025 RN - 333DO1RDJY (Serotonin) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Adult MH - Brain/drug effects/metabolism MH - Female MH - Humans MH - Male MH - N-Methyl-3,4-methylenedioxyamphetamine/*adverse effects MH - Neuropsychological Tests MH - Neurotoxicity Syndromes/metabolism/psychology MH - Pain Measurement MH - Pain Threshold/*psychology MH - Physical Stimulation MH - Regression Analysis MH - Serotonin/metabolism MH - Sleep/*drug effects MH - Substance Withdrawal Syndrome/metabolism/*psychology MH - Young Adult EDAT- 2011/05/24 06:00 MHDA- 2012/02/14 06:00 CRDT- 2011/05/24 06:00 PHST- 2010/10/15 00:00 [received] PHST- 2011/04/04 00:00 [accepted] PHST- 2011/05/24 06:00 [entrez] PHST- 2011/05/24 06:00 [pubmed] PHST- 2012/02/14 06:00 [medline] AID - 10.1007/s00213-011-2303-7 [doi] PST - ppublish SO - Psychopharmacology (Berl). 2011 Oct;217(4):475-84. doi: 10.1007/s00213-011-2303-7. Epub 2011 May 21.