Abstract
Treatment with 3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP), a potent and competitive N-methyl-D-aspartate antagonist, is able to reduce the hypoxia-induced increase in striatal dopamine level by 26% even after the hypoxic insult has occurred. The hypoxia-induced decrease of the striatal 3,4-dihydroxyphenylacetic acid level can also be reversed by CPP. This study demonstrates that CPP can antagonize the hypoxia-induced changes in the dopamine metabolism in the striatum of the newborn rat.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Dopamine / metabolism*
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Excitatory Amino Acid Antagonists / pharmacology
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Hypoxia, Brain / drug therapy*
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Hypoxia, Brain / physiopathology
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Neostriatum / drug effects*
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Neostriatum / physiopathology
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Neuroprotective Agents / pharmacology
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Piperazines / pharmacology*
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Rats
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Rats, Wistar
Substances
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Excitatory Amino Acid Antagonists
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Neuroprotective Agents
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Piperazines
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3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
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Dopamine