CPP antagonizes hypoxia-induced changes in dopamine metabolism in the striatum of newborn rat

Neurosci Res. 1999 Dec 30;35(4):347-50. doi: 10.1016/s0168-0102(99)00084-x.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Dopamine / metabolism*
  • Excitatory Amino Acid Antagonists / pharmacology
  • Hypoxia, Brain / drug therapy*
  • Hypoxia, Brain / physiopathology
  • Neostriatum / drug effects*
  • Neostriatum / physiopathology
  • Neuroprotective Agents / pharmacology
  • Piperazines / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Excitatory Amino Acid Antagonists
  • Neuroprotective Agents
  • Piperazines
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
  • Dopamine