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Oxidative metabolite of dopamine, 3,4-dihydroxyphenylacetaldehyde, induces dopamine release from PC12 cells by a Ca2+-independent mechanism.

Abstract
3,4-dihydroxyphenylacetaldehyde (DOPALD), an oxidative metabolite of dopamine (DA), induced dose-dependent DA release from pheochromocytoma (PC12) cells without affecting leakage of lactate dehydrogenase from the cells. DOPALD-induced DA release was independent of extracellular Ca2+ concentration and was not blocked by nifedipine, an L-type Ca2+ channel antagonist. These results indicated a novel intrinsic role of DOPALD in dopaminergic nerve terminals that may take part in the activation of dopamine neurons.
AuthorsTsuneichi Hashimoto, Chihiro Yabe-Nishimura
JournalBrain research (Brain Res) Vol. 931 Issue 1 Pg. 96-9 (Mar 22 2002) ISSN: 0006-8993 [Print] Netherlands
PMID11897094 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Calcium Channel Blockers
  • 3,4-Dihydroxyphenylacetic Acid
  • 3,4-dihydroxyphenylacetaldehyde
  • L-Lactate Dehydrogenase
  • Nifedipine
  • Calcium
  • Dopamine
Topics
  • 3,4-Dihydroxyphenylacetic Acid (analogs & derivatives, chemical synthesis, pharmacology)
  • Animals
  • Calcium (physiology)
  • Calcium Channel Blockers (pharmacology)
  • Dopamine (metabolism)
  • L-Lactate Dehydrogenase (metabolism)
  • Nifedipine (pharmacology)
  • Oxidation-Reduction
  • PC12 Cells
  • Parkinson Disease (metabolism)
  • Rats

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