Source:http://linkedlifedata.com/resource/pubmed/id/17359360
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-3-15
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pubmed:abstractText |
Prolonged neurotoxicity of the recreational drug, MDMA (3,4-methylenedioxymethamphetamine) on serotoninergic axon terminals has been suggested. The effect of a single (15 mg/kg) dose of intraperitoneally administered MDMA on serotoninergic fibre density, defined by tryptophan hydroxylase (TpH) and serotonin transporter (5-HTT) immunoreactivity, has been evaluated in the spinal cord and brain areas in Dark Agouti rats, 7 and 180 days after MDMA applications. Immunostaining for amyloid precursor protein (APP) has been performed to examine possible defects of the fast axonal transport, and 5-HTT mRNA expressions were quantified in neurones of medullary raphe nuclei. Seven days after MDMA treatment, a substantial decrease in the density of TpH-immunoreactive fibres was detectable in the frontal cortex, the caudate-putamen, the CA1 region of the hippocampus, and marked decreases were found in the spinal cord. These changes in TpH density showed a high correlation with 5-HTT densities. In contrast, APP-immunoreactive axonal bulbs were not detected in any of the brain regions studied. Seven days after MDMA administrations, significantly elevated 5-HTT mRNA expressions were found in the raphe pallidus and obscurus. Our results suggest that a single dose of MDMA elicits widespread depletion of TpH and 5-HTT immunoreactivity in serotoninergic axons without morphological sign of the blockage of the fast anterograde axonal transport. Our results do not support the notion of MDMA-induced axotomy of serotoninergic neurones. The up-regulation of 5-HTT mRNA expressions 1 week after MDMA injections might indicate the potential recovery of the serotonin system.
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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/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Plasma Membrane...,
http://linkedlifedata.com/resource/pubmed/chemical/Tryptophan Hydroxylase
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0305-1846
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
193-203
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pubmed:meshHeading |
pubmed-meshheading:17359360-Animals,
pubmed-meshheading:17359360-Axonal Transport,
pubmed-meshheading:17359360-Body Temperature,
pubmed-meshheading:17359360-Central Nervous System,
pubmed-meshheading:17359360-Gene Expression,
pubmed-meshheading:17359360-Immunohistochemistry,
pubmed-meshheading:17359360-Male,
pubmed-meshheading:17359360-N-Methyl-3,4-methylenedioxyamphetamine,
pubmed-meshheading:17359360-Nerve Fibers,
pubmed-meshheading:17359360-RNA, Messenger,
pubmed-meshheading:17359360-Rats,
pubmed-meshheading:17359360-Rats, Inbred Strains,
pubmed-meshheading:17359360-Serotonin,
pubmed-meshheading:17359360-Serotonin Agents,
pubmed-meshheading:17359360-Serotonin Plasma Membrane Transport Proteins,
pubmed-meshheading:17359360-Tryptophan Hydroxylase
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pubmed:year |
2007
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pubmed:articleTitle |
Single dose of MDMA causes extensive decrement of serotoninergic fibre density without blockage of the fast axonal transport in Dark Agouti rat brain and spinal cord.
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pubmed:affiliation |
Department of Neuropathology, National Institute of Psychiatry and Neurology, Budapest, Hungary.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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