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Daiichiro Nakahara

Researcher at Nagoya University

Publications -  29
Citations -  802

Daiichiro Nakahara is an academic researcher from Nagoya University. The author has contributed to research in topics: Microdialysis & Dopamine. The author has an hindex of 15, co-authored 29 publications receiving 786 citations.

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increased dopamine and serotonin metabolism in rat nucleus accumbens produced by intracranial self-stimulation of medial forebrain bundle as measured by in vivo microdialysis

TL;DR: Findings indicate that self-stimulation of the MFB in rats induces increases in both DA and serotonin activities in the NAC, which may be involved in mediating self- Stimulating the medial forebrain bundle.
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N-methylation of dopamine-derived 6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, (R)-salsolinol, in rat brains: in vivo microdialysis study.

TL;DR: N‐Methylation of (R)‐1‐methyl‐6,7‐dihydroxy‐1,2,3,4‐tetrahydroisoquinoline [(R]‐salsolinol] derived from dopamine was proved by in vivo microdialysis study in the rat brain to be an essential step for these alkaloids to increase their toxicity.
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Differential effect of self-stimulation on dopamine release and metabolism in the rat medial frontal cortex, nucleus accumbens and striatum studied by in vivo microdialysis.

TL;DR: The results indicate that self-stimulation of the MFB preferentially activates the mesocorticolimbic DA systems, thereby bilateral increases in the release of DA and its metabolism being produced in their terminal regions, the MFC and NAC.
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Simultaneous determination of in vivo hydroxylation of tyrosine and tryptophan in rat striatum by microdialysis-HPLC: relationship between dopamine and serotonin biosynthesis

TL;DR: The results suggest that L-DOPA and 5-HTP, the precursor amino acids for catecholamines and indoleamines, could affect mutually each other neuronal activity through the inhibition of their rate-limiting enzymes.
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Acute effects of 1-methyl-4-phenylpyridinium ion (MPP+) on dopamine and serotonin metabolism in rat striatum as assayed in vivo by a micro-dialysis technique.

TL;DR: By postmortem analysis of the striatal tissue MPP+ was proved to cause the inhibition of monoamine oxidase (MAO), especially MAO-B and the release of DA.