2026-04-17T16:41:11Zhttps://recercat.cat/oai/requestoai:recercat.cat:2445/986962025-12-05T14:25:36Zcom_2072_1057col_2072_478816col_2072_478917
RECERCAT
author
Abad, Sonia
author
Camarasa García, Jordi
author
Pubill Sánchez, David
author
Camins Espuny, Antoni
author
Escubedo Rafa, Elena
2016-05-19T15:57:37Z2016-12-21T23:01:21Z2015-12-212016-05-19T15:57:42Z
(±)3,4-Methylenedioxymethamphetamine (MDMA) is a relatively selective dopaminergic neurotoxin in mice. This study was designed to evaluate whether MDMA exposure affects their recognition memory and hippocampal expression of plasticity markers. Mice were administered with increasing doses of MDMA once per week for 8 weeks (three times in 1 day, every 3 h) and killed 2 weeks (2w) or 3 months (3m) later. The treatment did not modify hippocampal tryptophan hydroxylase 2, a serotonergic indicator, but induced an initial reduction in dopaminergic markers in substantia nigra, which remained stable for at least 3 months. In parallel, MDMA produced a decrease in dopamine (DA) levels in the striatum at 2w, which were restored 3 months later, suggesting dopaminergic terminal regeneration (sprouting phenomenon). Moreover, recognition memory was assessed using the object recognition test. Young (2w) and mature (3m) adult mice exhibited impaired memory after 24-h but not after just 1-h retention interval. Two weeks after the treatment, animals showed constant levels of CREB but an increase in its phosphorylated form and in c-Fos expression. Brain-derived neurotrophic factor (BDNF) and especially Arc overexpression was sustained and long-lasting. We cannot rule out the absence of MDMA injury in the hippocampus being due to the generation of BDNF. The levels of NMDAR2B, PSD-95, and synaptophysin were unaffected. In conclusion, the young mice exposed to MDMA showed increased expression of early key markers of plasticity, which sometimes remained for 3 months, and suggests hippocampal maladaptive plasticity that could explain memory deficits evidenced here.
(c) Humana Press., 2015 info:eu-repo/semantics/openAccess
Èxtasi (Droga)
Amfetamines
Hipocamp (Cervell)
Trastorns de la memòria
Ratolins (Animals de laboratori)
Ecstasy (Drug)
Amphetamines
Hippocampus (Brain)
Memory disorders
Mice (Laboratory animals)
Adaptive plasticity in the hippocampus of young mice intermittently exposed to MDMA could be the origin of memory deficits.
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion