Abstract |
We previously reported markedly reduced (-76%) dopamine (DA) levels in the putamen of seven patients with spinocerebellar ataxia type 1 ( SCA1) who had no evidence of nigral cell loss or parkinsonism. To determine whether the DA reduction was accompanied by loss of DA nerve terminals, we measured levels of the DA transporter ([3H] WIN, 35,428 binding; DA transporter protein) and the vesicular monoamine transporter ([3H]DTBZ binding) in the putamen of these patients. As compared with the controls (n = 14), mean putamen concentrations of [3H] WIN 35,428 binding (-45%), dopamine transporter protein (-61%), and [3H]DTBZ binding (-48%) were significantly reduced in this SCA1 subgroup. We conclude that the degeneration in nigrostriatal DA neurons begins at the nerve ending in SCA1.
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Authors | S J Kish, M Guttman, Y Robitaille, M el-Awar, L J Chang, A I Levey |
Journal | Neurology
(Neurology)
Vol. 48
Issue 4
Pg. 1109-11
(Apr 1997)
ISSN: 0028-3878 [Print] United States |
PMID | 9109912
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Biomarkers
- Carrier Proteins
- Dopamine Plasma Membrane Transport Proteins
- Dopamine Uptake Inhibitors
- Membrane Glycoproteins
- Membrane Transport Proteins
- Nerve Tissue Proteins
- dihydrotetrabenazine
- (1R-(exo,exo))-3-(4-fluorophenyl)-8-methyl-8- azabicyclo(3.2.1)octane-2-carboxylic acid, methyl ester
- Cocaine
- Dopamine
- Tetrabenazine
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Topics |
- Adult
- Biomarkers
- Cadaver
- Carrier Proteins
(metabolism)
- Cocaine
(analogs & derivatives, metabolism)
- Corpus Striatum
(metabolism)
- Dopamine
(metabolism)
- Dopamine Plasma Membrane Transport Proteins
- Dopamine Uptake Inhibitors
(metabolism)
- Humans
- Membrane Glycoproteins
- Membrane Transport Proteins
- Middle Aged
- Nerve Endings
(metabolism)
- Nerve Tissue Proteins
- Putamen
(metabolism)
- Spinocerebellar Degenerations
(metabolism, pathology)
- Substantia Nigra
(pathology)
- Tetrabenazine
(analogs & derivatives, metabolism)
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