Abstract
The two major metabolites of (+/-)3,4-methylenedioxyamphetamine (MDA), alpha-methyldopamine (alpha-MeDA) and 3-O-methyl-alpha-methyldopamine (3-O-Me-alpha-MeDA), were administered to rats intracerebroventricularly and into brain parenchyma. In addition, their precursors, (alpha-MeDOPA and 3-O-Me-alpha-MeDOPA, respectively) were administered systemically, individually and in combination. None of these treatments produced a lasting depletion of brain serotonin (5-HT). These findings suggest that neither of MDA's major metabolites mediate its toxic effects on 5-HT neurons and that either a minor metabolite is responsible or that alternate mechanisms are involved.
MeSH terms
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3,4-Methylenedioxyamphetamine / analogs & derivatives*
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3,4-Methylenedioxyamphetamine / metabolism
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3,4-Methylenedioxyamphetamine / toxicity*
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Animals
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Brain / drug effects
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Brain / metabolism*
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Brain / pathology
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Cerebral Cortex / metabolism
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Cerebral Ventricles / drug effects
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Cerebral Ventricles / physiology*
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Corpus Striatum / metabolism
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Deoxyepinephrine / administration & dosage
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Deoxyepinephrine / analogs & derivatives*
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Deoxyepinephrine / pharmacology
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Dopamine* / analogs & derivatives*
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Functional Laterality
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Hippocampus / metabolism
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Injections, Intraventricular
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Male
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Neurons / drug effects
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Neurons / metabolism*
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Neurons / pathology
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Organ Specificity
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Rats
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Rats, Inbred Strains
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Serotonin / metabolism*
Substances
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3-O-methyl-alpha-methyldopamine
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Serotonin
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3,4-Methylenedioxyamphetamine
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alpha-methyldopamine
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Deoxyepinephrine
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Dopamine