Movement Disorders (revue)

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Nigrostriatal Upregulation of 5-HT2A Receptors Correlates with Motor Dysfunction in Progressive Supranuclear Palsy

Identifieur interne : 000E48 ( PascalFrancis/Corpus ); précédent : 000E47; suivant : 000E49

Nigrostriatal Upregulation of 5-HT2A Receptors Correlates with Motor Dysfunction in Progressive Supranuclear Palsy

Auteurs : Maria Stamelou ; Andreas Matusch ; David Elmenhorst ; René Hurlemann ; Karla M. Eggert ; Karl Zilles ; Wolfgang H. Oertel ; Günter U. Höglinger ; Andreas Bauer

Source :

RBID : Pascal:09-0301991

Descripteurs français

English descriptors

Abstract

A dysfunction of multiple neurotransmitter systems is assumed as a neurochemical basis of the akinetic-rigid syndrome of progressive supranuclear palsy (PSP). In vitro studies have produced conflicting results on the serotoninergic system in PSP. We, therefore, studied the binding potential of the serotonin 2A (5-HT2A) receptor ligand [18F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT2A receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT2A receptor densities showed no changes upon partial-volume correction. Nigral and striatal receptor changes were significantly correlated with patients' scores of motor dysfunction (UPDRS III, PSP-rating scale) pointing to a functional relevance of the described findings.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 24
A06       @2 8
A08 01  1  ENG  @1 Nigrostriatal Upregulation of 5-HT2A Receptors Correlates with Motor Dysfunction in Progressive Supranuclear Palsy
A11 01  1    @1 STAMELOU (Maria)
A11 02  1    @1 MATUSCH (Andreas)
A11 03  1    @1 ELMENHORST (David)
A11 04  1    @1 HURLEMANN (René)
A11 05  1    @1 EGGERT (Karla M.)
A11 06  1    @1 ZILLES (Karl)
A11 07  1    @1 OERTEL (Wolfgang H.)
A11 08  1    @1 HÖGLINGER (Günter U.)
A11 09  1    @1 BAUER (Andreas)
A14 01      @1 Institute of Neuroscience and Biophysics-Medicine (INB-3), Research Center Jülich @2 Jülich @3 DEU @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 6 aut. @Z 9 aut.
A14 02      @1 Department of Neurology, Philipps University @2 Marburg @3 DEU @Z 1 aut. @Z 2 aut. @Z 5 aut. @Z 7 aut. @Z 8 aut.
A14 03      @1 Department of Psychiatry, University of Bonn @2 Bonn @3 DEU @Z 4 aut.
A14 04      @1 C. & O. Vogt Institute for Brain Research, University of Düsseldorf @2 Düsseldorf @3 DEU @Z 6 aut.
A14 05      @1 Department of Neurology, University of Düsseldorf @2 Düsseldorf @3 DEU @Z 9 aut.
A20       @1 1170-1175
A21       @1 2009
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000196165080090
A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
A45       @0 18 ref.
A47 01  1    @0 09-0301991
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 A dysfunction of multiple neurotransmitter systems is assumed as a neurochemical basis of the akinetic-rigid syndrome of progressive supranuclear palsy (PSP). In vitro studies have produced conflicting results on the serotoninergic system in PSP. We, therefore, studied the binding potential of the serotonin 2A (5-HT2A) receptor ligand [18F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT2A receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT2A receptor densities showed no changes upon partial-volume correction. Nigral and striatal receptor changes were significantly correlated with patients' scores of motor dysfunction (UPDRS III, PSP-rating scale) pointing to a functional relevance of the described findings.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Pathologie du système nerveux @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Récepteur sérotoninergique 5-HT2A @5 09
C03 02  X  ENG  @0 5-HT2A serotonin receptor @5 09
C03 02  X  SPA  @0 Receptor serotoninérgico 5-HT2A @5 09
C03 03  X  FRE  @0 Trouble fonctionnel @5 10
C03 03  X  ENG  @0 Dysfunction @5 10
C03 03  X  SPA  @0 Trastorno funcional @5 10
C03 04  X  FRE  @0 Sérotonine @2 NK @2 FR @5 11
C03 04  X  ENG  @0 Serotonin @2 NK @2 FR @5 11
C03 04  X  SPA  @0 Serotonina @2 NK @2 FR @5 11
C03 05  X  FRE  @0 Tomoscintigraphie @5 12
C03 05  X  ENG  @0 Emission tomography @5 12
C03 05  X  SPA  @0 Tomocentelleografía @5 12
C03 06  X  FRE  @0 Tomographie par émission de positons @5 13
C03 06  X  ENG  @0 Positron emission tomography @5 13
C03 06  X  SPA  @0 Tomografía emisión positrones @5 13
C07 01  X  FRE  @0 Neurotransmetteur @5 37
C07 01  X  ENG  @0 Neurotransmitter @5 37
C07 01  X  SPA  @0 Neurotransmisor @5 37
N21       @1 215
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 09-0301991 INIST
ET : Nigrostriatal Upregulation of 5-HT2A Receptors Correlates with Motor Dysfunction in Progressive Supranuclear Palsy
AU : STAMELOU (Maria); MATUSCH (Andreas); ELMENHORST (David); HURLEMANN (René); EGGERT (Karla M.); ZILLES (Karl); OERTEL (Wolfgang H.); HÖGLINGER (Günter U.); BAUER (Andreas)
AF : Institute of Neuroscience and Biophysics-Medicine (INB-3), Research Center Jülich/Jülich/Allemagne (1 aut., 2 aut., 3 aut., 6 aut., 9 aut.); Department of Neurology, Philipps University/Marburg/Allemagne (1 aut., 2 aut., 5 aut., 7 aut., 8 aut.); Department of Psychiatry, University of Bonn/Bonn/Allemagne (4 aut.); C. & O. Vogt Institute for Brain Research, University of Düsseldorf/Düsseldorf/Allemagne (6 aut.); Department of Neurology, University of Düsseldorf/Düsseldorf/Allemagne (9 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2009; Vol. 24; No. 8; Pp. 1170-1175; Bibl. 18 ref.
LA : Anglais
EA : A dysfunction of multiple neurotransmitter systems is assumed as a neurochemical basis of the akinetic-rigid syndrome of progressive supranuclear palsy (PSP). In vitro studies have produced conflicting results on the serotoninergic system in PSP. We, therefore, studied the binding potential of the serotonin 2A (5-HT2A) receptor ligand [18F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT2A receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT2A receptor densities showed no changes upon partial-volume correction. Nigral and striatal receptor changes were significantly correlated with patients' scores of motor dysfunction (UPDRS III, PSP-rating scale) pointing to a functional relevance of the described findings.
CC : 002B17; 002B17G
FD : Pathologie du système nerveux; Récepteur sérotoninergique 5-HT2A; Trouble fonctionnel; Sérotonine; Tomoscintigraphie; Tomographie par émission de positons
FG : Neurotransmetteur
ED : Nervous system diseases; 5-HT2A serotonin receptor; Dysfunction; Serotonin; Emission tomography; Positron emission tomography
EG : Neurotransmitter
SD : Sistema nervioso patología; Receptor serotoninérgico 5-HT2A; Trastorno funcional; Serotonina; Tomocentelleografía; Tomografía emisión positrones
LO : INIST-20953.354000196165080090
ID : 09-0301991

Links to Exploration step

Pascal:09-0301991

Le document en format XML

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<front>
<div type="abstract" xml:lang="en">A dysfunction of multiple neurotransmitter systems is assumed as a neurochemical basis of the akinetic-rigid syndrome of progressive supranuclear palsy (PSP). In vitro studies have produced conflicting results on the serotoninergic system in PSP. We, therefore, studied the binding potential of the serotonin 2A (5-HT
<sub>2A</sub>
) receptor ligand [
<sup>18</sup>
F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT
<sub>2A</sub>
receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT
<sub>2A</sub>
receptor densities showed no changes upon partial-volume correction. Nigral and striatal receptor changes were significantly correlated with patients' scores of motor dysfunction (UPDRS III, PSP-rating scale) pointing to a functional relevance of the described findings.</div>
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<sub>2A</sub>
) receptor ligand [
<sup>18</sup>
F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT
<sub>2A</sub>
receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT
<sub>2A</sub>
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<ET>Nigrostriatal Upregulation of 5-HT
<sub>2A</sub>
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<AU>STAMELOU (Maria); MATUSCH (Andreas); ELMENHORST (David); HURLEMANN (René); EGGERT (Karla M.); ZILLES (Karl); OERTEL (Wolfgang H.); HÖGLINGER (Günter U.); BAUER (Andreas)</AU>
<AF>Institute of Neuroscience and Biophysics-Medicine (INB-3), Research Center Jülich/Jülich/Allemagne (1 aut., 2 aut., 3 aut., 6 aut., 9 aut.); Department of Neurology, Philipps University/Marburg/Allemagne (1 aut., 2 aut., 5 aut., 7 aut., 8 aut.); Department of Psychiatry, University of Bonn/Bonn/Allemagne (4 aut.); C. & O. Vogt Institute for Brain Research, University of Düsseldorf/Düsseldorf/Allemagne (6 aut.); Department of Neurology, University of Düsseldorf/Düsseldorf/Allemagne (9 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2009; Vol. 24; No. 8; Pp. 1170-1175; Bibl. 18 ref.</SO>
<LA>Anglais</LA>
<EA>A dysfunction of multiple neurotransmitter systems is assumed as a neurochemical basis of the akinetic-rigid syndrome of progressive supranuclear palsy (PSP). In vitro studies have produced conflicting results on the serotoninergic system in PSP. We, therefore, studied the binding potential of the serotonin 2A (5-HT
<sub>2A</sub>
) receptor ligand [
<sup>18</sup>
F]altanserin in 8 patients with clinically probable PSP and 13 healthy controls using positron emission tomography. We found an up-regulation of 5-HT
<sub>2A</sub>
receptors in the substantia nigra and, to a lower degree, in the striatum, while neocortical 5- HT
<sub>2A</sub>
receptor densities showed no changes upon partial-volume correction. Nigral and striatal receptor changes were significantly correlated with patients' scores of motor dysfunction (UPDRS III, PSP-rating scale) pointing to a functional relevance of the described findings.</EA>
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