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Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor.

Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Research Abstract Details 

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  • Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Abstract Text:

    jennifer l amatoJennifer L Amato,michael g banksonMichael G Bankson,bryan k yamamotoBryan K Yamamoto,

    (+) 3,4,-Methylenedioxymethamphetamine (MDMA) is an abused drug that acutely releases serotonin (5-HT) and dopamine (DA) but produces long-term damage to 5-HT terminals. MDMA-induced DA release has been shown to be dampened by 5-HT. Although stress also activates the mesolimbic DA pathway, it is unknown if chronic stress after exposure to neurotoxic doses of MDMA will augment MDMA-induced DA release in the nucleus accumbens shell (NAcc(sh)). Rats were pretreated with MDMA (10 mg/kg x 4, intraperitoneal (i.p.)). After 7 days, rats were subjected to 10 days of chronic unpredictable stress. DA release in the NAcc(sh) and 5-HT in the ventral tegmental area (VTA) were measured after a challenge injection of MDMA (5 mg/kg, i.p.). The combination of pretreatment with MDMA+stress decreased basal concentrations of 5-HT in the VTA and DA in the NAcc(sh) and enhanced MDMA-stimulated DA release in the NAcc(sh). Pretreatment with MDMA or stress alone blunted MDMA-induced 5-HT release in the VTA. The augmentation of MDMA-induced DA release in rats pretreated with MDMA+chronic stress was attenuated by perfusion of the 5-HT(1B) antagonist, GR127935 into the VTA before the MDMA challenge injection. These results suggest that prior exposure to both MDMA and stress can produce a long-term augmentation in mesolimbic DA transmission and enhanced drug abuse vulnerability that is mediated, in part, by the 5-HT(1B) receptor in the VTA.

    Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Publishing Authors By Initials

    jl amatoJL Amato,mg banksonMG Bankson,bk yamamotoBK Yamamoto,

    For similar nervous system: central nervous system: brain: brain stem: mesencephalon: tegmentum mesencephali: ventral tegmental area research abstracts see: nervous system: central nervous system: brain: brain stem: mesencephalon: tegmentum mesencephali: ventral tegmental area research

    PUBMED ID PMID:

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    Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Neuropsychopharmacology : official publication of

    VOLUME: 32

    Page Numbers: 946-54

    Journal Abbreviation: Neuropsychopharmacology

    ISSN: 0893-133X

    DAY: 2

    MONTH: 08

    YEAR: 2006

    Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8904907

    Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Keywords Mesh Terms:

    KEYWORDS: Ventral Tegmental Area

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor. Information

    Substance Name: Dopamine

    Registry Number: 51-61-6

    Grant and Affiliation Information for Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor.

    AFFILIATION: Laboratory of Neurochemistry, Department of Pharmacology, Boston University School of Medicine, Boston, MA 02118, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDA

    GRANT: DA 16866

    ACRONYM: DA

    MEDLINETA: Neuropsychopharmacology

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    DATABASENAME:

    ACCESSION NUMBER:

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