La maladie de Parkinson au Canada (serveur d'exploration)

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Serotonin 2A Receptors and Visual Hallucinations in Parkinson Disease

Identifieur interne : 000447 ( PascalFrancis/Corpus ); précédent : 000446; suivant : 000448

Serotonin 2A Receptors and Visual Hallucinations in Parkinson Disease

Auteurs : Benedicte Ballanger ; Antonio P. Strafella ; Thilo Van Eimeren ; Mateusz Zurowski ; Pablo M. Rusjan ; Sylvain Houle ; Susan H. Fox

Source :

RBID : Pascal:10-0211459

Descripteurs français

English descriptors

Abstract

Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0003-9942
A02 01      @0 ARNEAS
A03   1    @0 Arch. neurol. : (Chic.)
A05       @2 67
A06       @2 4
A08 01  1  ENG  @1 Serotonin 2A Receptors and Visual Hallucinations in Parkinson Disease
A11 01  1    @1 BALLANGER (Benedicte)
A11 02  1    @1 STRAFELLA (Antonio P.)
A11 03  1    @1 VAN EIMEREN (Thilo)
A11 04  1    @1 ZUROWSKI (Mateusz)
A11 05  1    @1 RUSJAN (Pablo M.)
A11 06  1    @1 HOULE (Sylvain)
A11 07  1    @1 FOX (Susan H.)
A14 01      @1 Vivian M. Rakoff PET Centre and Centre for Addiction and Mental Health, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience @2 Toronto Western @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 5 aut. @Z 6 aut.
A14 02      @1 Movement Disorders Centre, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience @2 Toronto Western @3 USA @Z 2 aut. @Z 7 aut.
A14 03      @1 Department of Psychiatry, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience @2 Toronto Western @3 USA @Z 4 aut.
A14 04      @1 Research Institute , University Health Network, University of Toronto @2 Toronto, Ontario @3 CAN @Z 2 aut.
A20       @1 416-421
A21       @1 2010
A23 01      @0 ENG
A43 01      @1 INIST @2 2048B @5 354000181009750070
A44       @0 0000 @1 © 2010 INIST-CNRS. All rights reserved.
A45       @0 28 ref.
A47 01  1    @0 10-0211459
A60       @1 P
A61       @0 A
A64 01  1    @0 Archives of neurology : (Chicago)
A66 01      @0 USA
C01 01    ENG  @0 Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Hallucination visuelle @2 NM @5 01
C03 01  X  ENG  @0 Visual hallucination @2 NM @5 01
C03 01  X  SPA  @0 Alucinación visual @2 NM @5 01
C03 02  X  FRE  @0 Maladie de Parkinson @2 NM @5 02
C03 02  X  ENG  @0 Parkinson disease @2 NM @5 02
C03 02  X  SPA  @0 Parkinson enfermedad @2 NM @5 02
C03 03  X  FRE  @0 Pathologie du système nerveux @5 03
C03 03  X  ENG  @0 Nervous system diseases @5 03
C03 03  X  SPA  @0 Sistema nervioso patología @5 03
C03 04  X  FRE  @0 Récepteur sérotoninergique @5 09
C03 04  X  ENG  @0 Serotonine receptor @5 09
C03 04  X  SPA  @0 Receptor serotoninérgico @5 09
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Pathologie du système nerveux central @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
N21       @1 144
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 10-0211459 INIST
ET : Serotonin 2A Receptors and Visual Hallucinations in Parkinson Disease
AU : BALLANGER (Benedicte); STRAFELLA (Antonio P.); VAN EIMEREN (Thilo); ZUROWSKI (Mateusz); RUSJAN (Pablo M.); HOULE (Sylvain); FOX (Susan H.)
AF : Vivian M. Rakoff PET Centre and Centre for Addiction and Mental Health, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Movement Disorders Centre, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (2 aut., 7 aut.); Department of Psychiatry, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (4 aut.); Research Institute , University Health Network, University of Toronto/Toronto, Ontario/Canada (2 aut.)
DT : Publication en série; Niveau analytique
SO : Archives of neurology : (Chicago); ISSN 0003-9942; Coden ARNEAS; Etats-Unis; Da. 2010; Vol. 67; No. 4; Pp. 416-421; Bibl. 28 ref.
LA : Anglais
EA : Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.
CC : 002B17; 002B17G
FD : Hallucination visuelle; Maladie de Parkinson; Pathologie du système nerveux; Récepteur sérotoninergique
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central
ED : Visual hallucination; Parkinson disease; Nervous system diseases; Serotonine receptor
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD : Alucinación visual; Parkinson enfermedad; Sistema nervioso patología; Receptor serotoninérgico
LO : INIST-2048B.354000181009750070
ID : 10-0211459

Links to Exploration step

Pascal:10-0211459

Le document en format XML

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<div type="abstract" xml:lang="en">Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.</div>
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<s1>Department of Psychiatry, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience</s1>
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<s3>USA</s3>
<sZ>4 aut.</sZ>
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<fA14 i1="04">
<s1>Research Institute , University Health Network, University of Toronto</s1>
<s2>Toronto, Ontario</s2>
<s3>CAN</s3>
<sZ>2 aut.</sZ>
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<s0>Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.</s0>
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<s2>NM</s2>
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<s5>03</s5>
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<s5>03</s5>
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<s5>09</s5>
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<s0>Encéfalo patología</s0>
<s5>37</s5>
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<s0>Syndrome extrapyramidal</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Pathologie du système nerveux central</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>40</s5>
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<s1>144</s1>
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<NO>PASCAL 10-0211459 INIST</NO>
<ET>Serotonin 2A Receptors and Visual Hallucinations in Parkinson Disease</ET>
<AU>BALLANGER (Benedicte); STRAFELLA (Antonio P.); VAN EIMEREN (Thilo); ZUROWSKI (Mateusz); RUSJAN (Pablo M.); HOULE (Sylvain); FOX (Susan H.)</AU>
<AF>Vivian M. Rakoff PET Centre and Centre for Addiction and Mental Health, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (1 aut., 2 aut., 3 aut., 5 aut., 6 aut.); Movement Disorders Centre, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (2 aut., 7 aut.); Department of Psychiatry, Toronto Western Hospital, and Division of Brain, Imaging and Behaviour-Systems Neuroscience/Toronto Western/Etats-Unis (4 aut.); Research Institute , University Health Network, University of Toronto/Toronto, Ontario/Canada (2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Archives of neurology : (Chicago); ISSN 0003-9942; Coden ARNEAS; Etats-Unis; Da. 2010; Vol. 67; No. 4; Pp. 416-421; Bibl. 28 ref.</SO>
<LA>Anglais</LA>
<EA>Background: Complex visual hallucinations (VHs) occur in several pathologic conditions; however, the neural mechanisms underlying these symptoms remain unclear. Although dopamine may have a role, indirect evidence indicates that serotonin may also contribute to the pathogenesis of complex VHs, probably via involvement of the serotonin 2 receptor. Objective: To examine for the first time in vivo changes in serotonin 2A receptor neurotransmission among patients having Parkinson disease (PD) with VHs. Design: Case-control study. Setting: Academic research. Patients: Seven patients having PD with VHs and 7 age-matched patients having PD without VHs were recruited. Main Outcome Measures: We used the selective serotonin 2A receptor ligand setoperone F 18 during positron emission tomography among nondemented patients having PD with VHs. Results: Patients having PD with VHs demonstrate increased serotonin 2A receptor binding in the ventral visual pathway (including the bilateral inferooccipital gyrus, right fusiform gyrus, and inferotemporal cortex) as well as the bilateral dorsolateral prefrontal cortex, medial orbitofrontal cortex, and insula. Conclusions: This pilot study provides the first in vivo evidence suggesting a role for serotonin 2A receptors in mediating VHs via the ventral visual pathway in PD. Treatment studies should be performed using selective serotonin 2A receptor antagonists, which have important implications for the clinical management of VHs and psychosis in PD.</EA>
<CC>002B17; 002B17G</CC>
<FD>Hallucination visuelle; Maladie de Parkinson; Pathologie du système nerveux; Récepteur sérotoninergique</FD>
<FG>Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central</FG>
<ED>Visual hallucination; Parkinson disease; Nervous system diseases; Serotonine receptor</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease</EG>
<SD>Alucinación visual; Parkinson enfermedad; Sistema nervioso patología; Receptor serotoninérgico</SD>
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<ID>10-0211459</ID>
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