Brain dopamine-stimulated adenylyl cyclase activity in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy
Identifieur interne : 000974 ( PascalFrancis/Corpus ); précédent : 000973; suivant : 000975Brain dopamine-stimulated adenylyl cyclase activity in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy
Auteurs : Junchao Tong ; Paul S. Fitzmaurice ; Lee Cyn Ang ; Yoshiaki Furukawa ; Mark Gunman ; Stephen J. KishSource :
- Annals of neurology [ 0364-5134 ] ; 2004.
Descripteurs français
- Pascal (Inist)
English descriptors
Abstract
The dopamine D1 receptor is considered to participate in levodopa's antiparkinsonian action and levodopa-induced dyskinesias. We examined the functional status of the D1 receptor in brain of patients with Parkinson's disease (PD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). Dopamine-stimulated adenylyl cyclase activity was significantly increased in putamen (+43%) and frontal cortex (+52%) in PD, normal in PSP, but decreased by 47% in putamen in MSA. The supersensitive dopamine D1 receptors in both striatum and cerebral cortex in PD might compensate for dopamine deficiency, but could also contribute to long-term complications of levodopa therapy.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
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Format Inist (serveur)
NO : | PASCAL 04-0448985 INIST |
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ET : | Brain dopamine-stimulated adenylyl cyclase activity in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy |
AU : | TONG (Junchao); FITZMAURICE (Paul S.); ANG (Lee Cyn); FURUKAWA (Yoshiaki); GUNMAN (Mark); KISH (Stephen J.) |
AF : | Human Neurochemical Pathology Laboratory, Center for Addiction and Mental Health/Toronto/Canada (1 aut., 2 aut., 5 aut., 6 aut.); Division of Neuropathology, London Health Science Center, University of Western Ontario/London/Royaume-Uni (3 aut.); Movement Disorder Research Laboratory, Center for Addiction and Mental Health/Toronto, Ontario/Canada (4 aut.) |
DT : | Publication en série; Courte communication, note brève; Niveau analytique |
SO : | Annals of neurology; ISSN 0364-5134; Coden ANNED3; Etats-Unis; Da. 2004; Vol. 55; No. 1; Pp. 125-129; Bibl. 20 ref. |
LA : | Anglais |
EA : | The dopamine D1 receptor is considered to participate in levodopa's antiparkinsonian action and levodopa-induced dyskinesias. We examined the functional status of the D1 receptor in brain of patients with Parkinson's disease (PD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). Dopamine-stimulated adenylyl cyclase activity was significantly increased in putamen (+43%) and frontal cortex (+52%) in PD, normal in PSP, but decreased by 47% in putamen in MSA. The supersensitive dopamine D1 receptors in both striatum and cerebral cortex in PD might compensate for dopamine deficiency, but could also contribute to long-term complications of levodopa therapy. |
CC : | 002B17 |
FD : | Parkinson maladie; Dopamine; Atrophie multisystématisée; Paralysie; Système nerveux pathologie |
FG : | Encéphale pathologie; Système nerveux central; Catécholamine; Neurotransmetteur; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie; Trouble moteur; Trouble neurologique |
ED : | Parkinson disease; Dopamine; Multiple system atrophy; Paralysis; Nervous system diseases |
EG : | Cerebral disorder; Central nervous system; Catecholamine; Neurotransmitter; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Motor system disorder; Neurological disorder |
SD : | Parkinson enfermedad; Dopamina; Atrofia multisistematizada; Parálisis; Sistema nervioso patología |
LO : | INIST-16555.354000113877770180 |
ID : | 04-0448985 |
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Pascal:04-0448985Le document en format XML
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<front><div type="abstract" xml:lang="en">The dopamine D<sub>1</sub>
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<ET>Brain dopamine-stimulated adenylyl cyclase activity in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy</ET>
<AU>TONG (Junchao); FITZMAURICE (Paul S.); ANG (Lee Cyn); FURUKAWA (Yoshiaki); GUNMAN (Mark); KISH (Stephen J.)</AU>
<AF>Human Neurochemical Pathology Laboratory, Center for Addiction and Mental Health/Toronto/Canada (1 aut., 2 aut., 5 aut., 6 aut.); Division of Neuropathology, London Health Science Center, University of Western Ontario/London/Royaume-Uni (3 aut.); Movement Disorder Research Laboratory, Center for Addiction and Mental Health/Toronto, Ontario/Canada (4 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Annals of neurology; ISSN 0364-5134; Coden ANNED3; Etats-Unis; Da. 2004; Vol. 55; No. 1; Pp. 125-129; Bibl. 20 ref.</SO>
<LA>Anglais</LA>
<EA>The dopamine D<sub>1</sub>
receptor is considered to participate in levodopa's antiparkinsonian action and levodopa-induced dyskinesias. We examined the functional status of the D<sub>1</sub>
receptor in brain of patients with Parkinson's disease (PD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). Dopamine-stimulated adenylyl cyclase activity was significantly increased in putamen (+43%) and frontal cortex (+52%) in PD, normal in PSP, but decreased by 47% in putamen in MSA. The supersensitive dopamine D<sub>1</sub>
receptors in both striatum and cerebral cortex in PD might compensate for dopamine deficiency, but could also contribute to long-term complications of levodopa therapy.</EA>
<CC>002B17</CC>
<FD>Parkinson maladie; Dopamine; Atrophie multisystématisée; Paralysie; Système nerveux pathologie</FD>
<FG>Encéphale pathologie; Système nerveux central; Catécholamine; Neurotransmetteur; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie; Trouble moteur; Trouble neurologique</FG>
<ED>Parkinson disease; Dopamine; Multiple system atrophy; Paralysis; Nervous system diseases</ED>
<EG>Cerebral disorder; Central nervous system; Catecholamine; Neurotransmitter; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Motor system disorder; Neurological disorder</EG>
<SD>Parkinson enfermedad; Dopamina; Atrofia multisistematizada; Parálisis; Sistema nervioso patología</SD>
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