PMID- 14751419 OWN - NLM STAT- MEDLINE DCOM- 20040528 LR - 20190911 IS - 0278-5846 (Print) IS - 0278-5846 (Linking) VI - 28 IP - 2 DP - 2004 Mar TI - Anxiogenic-like activity of 3,4-methylenedioxy-methamphetamine ("Ecstasy") in the social interaction test is accompanied by an increase of c-fos expression in mice amygdala. PG - 249-54 AB - 3,4-Methylenedioxymethamphetamine (MDMA) is a synthetic amphetamine popularly known as "Ecstasy." Animal studies examining acute effects of MDMA on anxiety are unclear because although an anxiolytic-like action of MDMA in different animal models of anxiety has been described, there is also substantial evidence supporting an anxiogenic-like effect of this drug. To date, several studies have examined c-fos expression following MDMA administration in rats. However, there is no information about the MDMA-induced c-fos expression in mice previously tested in an animal model of anxiety. In this study, male mice were injected with MDMA (1, 8 and 15 mg/kg ip) and assessed for changes on anxiety and for the expression of the immediate early gene c-fos in the amygdala (central, basolateral and basomedial). Anxiety was evaluated by the "social interaction test." Ten behavioral categories were recorded: body care, digging, nonsocial exploration, exploration from a distance, social investigation, threat, attack, avoidance/flee, defense/submission and immobility. As compared with the control group, mice treated with MDMA (all doses) showed a decrease in mean duration and total time spent in social investigation behaviors, whereas avoidance/flee behaviors were significantly increased after treatment with this compound (8 and 15 mg/kg). Likewise, a significant increase in c-fos expression was found in the basolateral (all doses) and central (15 mg/kg) amygdala after MDMA administration. Overall, these findings indicate that MDMA exhibits an anxiogenic-like profile in the social interaction test in mice, and that central and basolateral amygdala might be involved in these anxiogenic-like effects of the drug. FAU - Navarro, Jose Francisco AU - Navarro JF AD - Department of Psychobiology, Faculty of Psychology, University of Malaga, Campus de Teatinos, s/n 29071 Malaga, Spain. navahuma@uma.es FAU - Rivera, Alicia AU - Rivera A FAU - Maldonado, Enrique AU - Maldonado E FAU - Cavas, Maria AU - Cavas M FAU - de la Calle, Adelaida AU - de la Calle A LA - eng PT - Comparative Study PT - Journal Article PL - England TA - Prog Neuropsychopharmacol Biol Psychiatry JT - Progress in neuro-psychopharmacology & biological psychiatry JID - 8211617 RN - 0 (Hallucinogens) RN - 0 (Proto-Oncogene Proteins c-fos) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Amygdala/*drug effects/metabolism MH - Animals MH - Behavior, Animal MH - Cell Count/methods MH - Dose-Response Relationship, Drug MH - Gene Expression/drug effects MH - Hallucinogens/*pharmacology MH - Immunohistochemistry/methods MH - *Interpersonal Relations MH - Male MH - Mice MH - N-Methyl-3,4-methylenedioxyamphetamine/*pharmacology MH - Proto-Oncogene Proteins c-fos/*metabolism MH - Statistics, Nonparametric EDAT- 2004/01/31 05:00 MHDA- 2004/05/29 05:00 CRDT- 2004/01/31 05:00 PHST- 2004/01/31 05:00 [pubmed] PHST- 2004/05/29 05:00 [medline] PHST- 2004/01/31 05:00 [entrez] AID - S0278584603002513 [pii] AID - 10.1016/j.pnpbp.2003.10.016 [doi] PST - ppublish SO - Prog Neuropsychopharmacol Biol Psychiatry. 2004 Mar;28(2):249-54. doi: 10.1016/j.pnpbp.2003.10.016.