Monoamine vesicular uptake sites in patients with Parkinson's disease and Alzheimer's disease, as measured by tritiated dihydrotetrabenazine autoradiography
Identifieur interne : 004A06 ( Main/Exploration ); précédent : 004A05; suivant : 004A07Monoamine vesicular uptake sites in patients with Parkinson's disease and Alzheimer's disease, as measured by tritiated dihydrotetrabenazine autoradiography
Auteurs : Stéphane Lehéricy [France] ; Jean-Philippe Brandel [France] ; Etienne C. Hirsch [France] ; Philippe Anglade [France] ; Joao Villares [France] ; Daniel Scherman [France] ; Charles Duyckaerts [France] ; France Javoy-Agid [France] ; Yves Agid [France]Source :
- Brain Research [ 0006-8993 ] ; 1994.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Aged, Aged, 80 and over, Alzheimer Disease (metabolism), Alzheimer disease, Autoradiography, Binding Sites, Biogenic Monoamines (metabolism), Caudate nucleus, Comparative study, Corpus Striatum (metabolism), Corpus striatum, Dopamine, Dopaminergic neuron, Exploration, Female, Human, Human brain, Humans, Male, Matrix, Middle Aged, Monoamine, Parkinson Disease (metabolism), Parkinson disease, Putamen, Reference Values, Striosome, Tetrabenazine (analogs & derivatives), Tetrabenazine (metabolism), Tritium, Ventral striatum.
- MESH :
- chemical , analogs & derivatives : Tetrabenazine.
- chemical , metabolism : Biogenic Monoamines, Tetrabenazine.
- metabolism : Alzheimer Disease, Corpus Striatum, Parkinson Disease.
- Aged, Aged, 80 and over, Autoradiography, Binding Sites, Female, Humans, Male, Middle Aged, Reference Values, Tritium.
Abstract
The monoaminergic innervation of the caudate nucleus, putamen and ventral striatum was investigated post mortem, in patients with Parkinson's and Alzheimer's disease as compared to control subjects, by autoradiographic detection of tritiated dihydrotetrabenazine (3H-TBZOH), a specific high affinity ligand of the vesicular monoamine transporter. The binding of 3H-TBZOH was specific and saturable (Kd 5.3 nM). In control striatum, the pattern of distribution of 3H-TBZOH binding was heterogeneous, with higher binding levels in the ‘matrix’ than in the ‘striosome’ compartment. Changes in ligand binding levels were observed in the pathological brains compared to controls. In Parkinson's disease (PD), characterized by a severe damage of mesostriatal dopaminergic neurons, the density of 3H-TBZOH binding was reduced. A severe decrease in 3H-TBZOH binding was observed in all parts of the striatum (caudate nucleus: −80%, putamen: −86%, ventral striatum: −94%) in PD brains. The data corroborate the deficiency in striatal dopaminergic transmission and suggest that in PD brains dopaminergic terminals have disappeared and/or no longer contain synaptic vesicles. In Alzheimer's disease (AD), 3H-TBZOH binding was significantly reduced by 57% in the ventral striatum and not in the caudate nucleus and putamen. The specific decrease of monoaminergic transporter levels in the ventral striatum confirm that this nucleus is a target area in AD.
Url:
DOI: 10.1016/0006-8993(94)90856-7
Affiliations:
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Le document en format XML
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<term>Aged, 80 and over</term>
<term>Alzheimer Disease (metabolism)</term>
<term>Alzheimer disease</term>
<term>Autoradiography</term>
<term>Binding Sites</term>
<term>Biogenic Monoamines (metabolism)</term>
<term>Caudate nucleus</term>
<term>Comparative study</term>
<term>Corpus Striatum (metabolism)</term>
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<term>Dopaminergic neuron</term>
<term>Exploration</term>
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<term>Human</term>
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<term>Humans</term>
<term>Male</term>
<term>Matrix</term>
<term>Middle Aged</term>
<term>Monoamine</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson disease</term>
<term>Putamen</term>
<term>Reference Values</term>
<term>Striosome</term>
<term>Tetrabenazine (analogs & derivatives)</term>
<term>Tetrabenazine (metabolism)</term>
<term>Tritium</term>
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<front><div type="abstract" xml:lang="en">The monoaminergic innervation of the caudate nucleus, putamen and ventral striatum was investigated post mortem, in patients with Parkinson's and Alzheimer's disease as compared to control subjects, by autoradiographic detection of tritiated dihydrotetrabenazine (3H-TBZOH), a specific high affinity ligand of the vesicular monoamine transporter. The binding of 3H-TBZOH was specific and saturable (Kd 5.3 nM). In control striatum, the pattern of distribution of 3H-TBZOH binding was heterogeneous, with higher binding levels in the ‘matrix’ than in the ‘striosome’ compartment. Changes in ligand binding levels were observed in the pathological brains compared to controls. In Parkinson's disease (PD), characterized by a severe damage of mesostriatal dopaminergic neurons, the density of 3H-TBZOH binding was reduced. A severe decrease in 3H-TBZOH binding was observed in all parts of the striatum (caudate nucleus: −80%, putamen: −86%, ventral striatum: −94%) in PD brains. The data corroborate the deficiency in striatal dopaminergic transmission and suggest that in PD brains dopaminergic terminals have disappeared and/or no longer contain synaptic vesicles. In Alzheimer's disease (AD), 3H-TBZOH binding was significantly reduced by 57% in the ventral striatum and not in the caudate nucleus and putamen. The specific decrease of monoaminergic transporter levels in the ventral striatum confirm that this nucleus is a target area in AD.</div>
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