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.
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Authors | Tsuneichi Hashimoto, Chihiro Yabe-Nishimura |
Journal | Brain research
(Brain Res)
Vol. 931
Issue 1
Pg. 96-9
(Mar 22 2002)
ISSN: 0006-8993 [Print] Netherlands |
PMID | 11897094
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Calcium Channel Blockers
- 3,4-Dihydroxyphenylacetic Acid
- 3,4-dihydroxyphenylacetaldehyde
- L-Lactate Dehydrogenase
- Nifedipine
- Calcium
- Dopamine
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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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