Source:http://linkedlifedata.com/resource/pubmed/id/16885935
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-3-15
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pubmed:abstractText |
(+) 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.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/N-Methyl-3,4-methylenedioxyamphetami...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Serotonin, 5-HT1B,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Agents
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0893-133X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
946-54
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pubmed:dateRevised |
2011-5-18
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pubmed:meshHeading |
pubmed-meshheading:16885935-Analysis of Variance,
pubmed-meshheading:16885935-Animals,
pubmed-meshheading:16885935-Dopamine,
pubmed-meshheading:16885935-Electrochemistry,
pubmed-meshheading:16885935-Male,
pubmed-meshheading:16885935-N-Methyl-3,4-methylenedioxyamphetamine,
pubmed-meshheading:16885935-Nucleus Accumbens,
pubmed-meshheading:16885935-Rats,
pubmed-meshheading:16885935-Rats, Sprague-Dawley,
pubmed-meshheading:16885935-Receptor, Serotonin, 5-HT1B,
pubmed-meshheading:16885935-Serotonin,
pubmed-meshheading:16885935-Serotonin Agents,
pubmed-meshheading:16885935-Stress, Physiological,
pubmed-meshheading:16885935-Ventral Tegmental Area
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pubmed:year |
2007
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pubmed:articleTitle |
Prior exposure to chronic stress and MDMA potentiates mesoaccumbens dopamine release mediated by the 5-HT(1B) receptor.
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pubmed:affiliation |
Laboratory of Neurochemistry, Department of Pharmacology, Boston University School of Medicine, Boston, MA 02118, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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