Abstract
When administered to mice pretreated with the monoamine-depleter reserpine and the catecholamine synthesis inhibitor alpha-methyl-para-tyrosine, the preferential autoreceptor antagonists (+)-AJ76 and (+)-UH 232 induced weak locomotor stimulation. When either (+)-AJ 76 or (+)-UH 232 was combined with a subthreshold dose of the selective NMDA antagonist dizocilpine (MK-801), a marked locomotor stimulation was produced in monoamine-depleted mice. The mechanism of this stimulation, although reduced by dopamine antagonists, remains to be clarified.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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8-Hydroxy-2-(di-n-propylamino)tetralin* / analogs & derivatives*
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Animals
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Dizocilpine Maleate / metabolism
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Dizocilpine Maleate / pharmacology
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Dopamine Antagonists*
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Drug Synergism
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Locomotion / drug effects
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Locomotion / physiology*
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Male
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Mice
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Motor Activity / drug effects*
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Motor Activity / physiology
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N-Methylaspartate / antagonists & inhibitors
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Tetrahydronaphthalenes / metabolism
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Tetrahydronaphthalenes / pharmacology*
Substances
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Dopamine Antagonists
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Tetrahydronaphthalenes
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N-Methylaspartate
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Dizocilpine Maleate
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8-Hydroxy-2-(di-n-propylamino)tetralin
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5-methoxy-1-methyl-2-(n-propylamino)tetralin
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UH 232