PMID- 18403002 OWN - NLM STAT- MEDLINE DCOM- 20080812 LR - 20240312 IS - 0091-3057 (Print) IS - 0091-3057 (Linking) VI - 90 IP - 2 DP - 2008 Aug TI - Locomotor stimulation produced by 3,4-methylenedioxymethamphetamine (MDMA) is correlated with dialysate levels of serotonin and dopamine in rat brain. PG - 208-17 LID - 10.1016/j.pbb.2008.02.018 [doi] AB - (+/-)-3,4-Methylenedioxymethamphetamine (MDMA, or Ecstasy) is an illicit drug that evokes transporter-mediated release of monoamines, including serotonin (5-HT) and dopamine (DA). Here we monitored the effects of MDMA on neurochemistry and motor activity in rats, as a means to evaluate relationships between 5-HT, DA, and behavior. Male rats undergoing in vivo microdialysis were housed in chambers equipped with photobeams for measurement of ambulation (i.e., forward locomotion) and stereotypy (i.e., head weaving and forepaw treading). Microdialysis probes were placed into the n. accumbens, striatum or prefrontal cortex in separate groups of rats. Dialysate samples were assayed for 5-HT and DA by microbore HPLC-ECD. Rats received two i.v. injections of MDMA, 1 mg/kg followed by 3 mg/kg 60 min later; neurochemical and locomotor parameters were measured concurrently. MDMA produced dose-related elevations in extracellular 5-HT and DA in all regions, with the magnitude of 5-HT release always exceeding that of DA release. MDMA-induced ambulation was positively correlated with dialysate DA levels in all regions (P<0.05-0.0001) and with dialysate 5-HT in striatum and cortex (P<0.001-0.0001). Stereotypy was strongly correlated with dialysate 5-HT in all areas (P<0.001-0.0001) and with dialysate DA in accumbens and striatum (P<0.001-0.0001). These data support previous work and suggest the complex spectrum of behaviors produced by MDMA involves 5-HT and DA in a region- and modality-specific manner. FAU - Baumann, Michael H AU - Baumann MH AD - Clinical Psychopharmacology Section, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, United States. mbaumann@mail.nih.gov FAU - Clark, Robert D AU - Clark RD FAU - Rothman, Richard B AU - Rothman RB LA - eng GR - Z99 DA999999/ImNIH/Intramural NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Intramural DEP - 20080304 PL - United States TA - Pharmacol Biochem Behav JT - Pharmacology, biochemistry, and behavior JID - 0367050 RN - 0 (Receptor, Serotonin, 5-HT2C) RN - 333DO1RDJY (Serotonin) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) RN - VTD58H1Z2X (Dopamine) SB - IM MH - Animals MH - Corpus Striatum/drug effects/metabolism MH - Dopamine/*metabolism/physiology MH - Male MH - *Microdialysis MH - Motor Activity/*drug effects MH - N-Methyl-3,4-methylenedioxyamphetamine/*pharmacology MH - Nucleus Accumbens/drug effects/metabolism MH - Prefrontal Cortex/drug effects/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Receptor, Serotonin, 5-HT2C/physiology MH - Serotonin/*metabolism/physiology PMC - PMC2491560 MID - NIHMS55860 EDAT- 2008/04/12 09:00 MHDA- 2008/08/13 09:00 PMCR- 2009/08/01 CRDT- 2008/04/12 09:00 PHST- 2007/07/24 00:00 [received] PHST- 2007/12/27 00:00 [revised] PHST- 2008/02/19 00:00 [accepted] PHST- 2008/04/12 09:00 [pubmed] PHST- 2008/08/13 09:00 [medline] PHST- 2008/04/12 09:00 [entrez] PHST- 2009/08/01 00:00 [pmc-release] AID - S0091-3057(08)00065-8 [pii] AID - 10.1016/j.pbb.2008.02.018 [doi] PST - ppublish SO - Pharmacol Biochem Behav. 2008 Aug;90(2):208-17. doi: 10.1016/j.pbb.2008.02.018. Epub 2008 Mar 4.