La maladie de Parkinson en France (serveur d'exploration)

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Antidyskinetic effect of A2A and 5HT1A/1B receptor ligands in two animal models of Parkinson's disease.

Identifieur interne : 000207 ( PubMed/Checkpoint ); précédent : 000206; suivant : 000208

Antidyskinetic effect of A2A and 5HT1A/1B receptor ligands in two animal models of Parkinson's disease.

Auteurs : Annalisa Pinna [Italie] ; Wai Kin D. Ko [Royaume-Uni] ; Giulia Costa [Italie] ; Elisabetta Tronci [Italie] ; Camino Fidalgo [Italie] ; Nicola Simola [Italie] ; Qin Li [Royaume-Uni] ; Mojgan Aghazadeh Tabrizi [Italie] ; Erwan Bezard [Royaume-Uni] ; Manolo Carta [Italie] ; Micaela Morelli [Italie]

Source :

RBID : pubmed:26871939

English descriptors

Abstract

The serotonin 5-HT1A/1B receptor agonist eltoprazine suppressed dyskinetic-like behavior in animal models of Parkinson's disease (PD) but simultaneously reduced levodopa (l-dopa)-induced motility. Moreover, adenosine A2A receptor antagonists, such as preladenant, significantly increased l-dopa efficacy in PD without exacerbating dyskinetic-like behavior.

DOI: 10.1002/mds.26475
PubMed: 26871939


Affiliations:


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pubmed:26871939

Le document en format XML

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<term>Animals</term>
<term>Antiparkinson Agents (administration & dosage)</term>
<term>Antiparkinson Agents (adverse effects)</term>
<term>Antiparkinson Agents (pharmacology)</term>
<term>Behavior, Animal (drug effects)</term>
<term>Disease Models, Animal</term>
<term>Drug Therapy, Combination</term>
<term>Dyskinesia, Drug-Induced (drug therapy)</term>
<term>Dyskinesia, Drug-Induced (prevention & control)</term>
<term>Female</term>
<term>Levodopa (administration & dosage)</term>
<term>Levodopa (adverse effects)</term>
<term>Levodopa (pharmacology)</term>
<term>Macaca fascicularis</term>
<term>Male</term>
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<term>Piperazines (pharmacology)</term>
<term>Pyrimidines (administration & dosage)</term>
<term>Pyrimidines (pharmacology)</term>
<term>Rats</term>
<term>Rats, Sprague-Dawley</term>
<term>Serotonin Receptor Agonists (administration & dosage)</term>
<term>Serotonin Receptor Agonists (pharmacology)</term>
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<term>Behavior, Animal</term>
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<term>Dyskinesia, Drug-Induced</term>
<term>Parkinson Disease</term>
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<div type="abstract" xml:lang="en">The serotonin 5-HT1A/1B receptor agonist eltoprazine suppressed dyskinetic-like behavior in animal models of Parkinson's disease (PD) but simultaneously reduced levodopa (l-dopa)-induced motility. Moreover, adenosine A2A receptor antagonists, such as preladenant, significantly increased l-dopa efficacy in PD without exacerbating dyskinetic-like behavior.</div>
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<DateCreated>
<Year>2016</Year>
<Month>04</Month>
<Day>15</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>01</Month>
<Day>17</Day>
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<Year>2017</Year>
<Month>01</Month>
<Day>17</Day>
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<ISSN IssnType="Electronic">1531-8257</ISSN>
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<Volume>31</Volume>
<Issue>4</Issue>
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<Year>2016</Year>
<Month>Apr</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Antidyskinetic effect of A2A and 5HT1A/1B receptor ligands in two animal models of Parkinson's disease.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The serotonin 5-HT1A/1B receptor agonist eltoprazine suppressed dyskinetic-like behavior in animal models of Parkinson's disease (PD) but simultaneously reduced levodopa (l-dopa)-induced motility. Moreover, adenosine A2A receptor antagonists, such as preladenant, significantly increased l-dopa efficacy in PD without exacerbating dyskinetic-like behavior.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">We evaluated whether a combination of eltoprazine and preladenant may prevent or suppress l-dopa-induced dyskinesia, without impairing l-dopa's efficacy in relieving motor signs, in 2 PD models: unilateral 6-hydroxydopamine-lesioned rats and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated monkeys.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Rotational behavior and abnormal involuntary movements, or disability and l-dopa-induced dyskinesia were evaluated in 6-hydroxydopamine-lesioned rats and MPTP-treated monkeys, respectively. Moreover, in the rodent striatum, induction of immediate-early gene zif-268, an index of long-term changes, was correlated with dyskinesia.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">In 6-hydroxydopamine-lesioned rats, combined administration of l-dopa (4 mg/kg) plus eltoprazine (0.6 mg/kg) plus preladenant (0.3 mg/kg) significantly prevented or reduced dyskinetic-like behavior without impairing motor activity. Zif-268 was increased in the striatum of rats treated with l-dopa and l-dopa plus preladenant compared with vehicle. In contrast, rats treated with eltoprazine (with or without preladenant) had lower zif-268 activation after chronic treatment in both the dyskinetic and l-dopa-non-primed groups. Moreover, acute l-dopa plus eltoprazine plus preladenant prevented worsening of motor performance (adjusting step) and sensorimotor integration deficit. Similar results were obtained in MPTP-treated monkeys, where a combination of preladenant with eltoprazine was found to counteract dyskinesia and maintain the full therapeutic effects of a low dose of l-dopa.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Our results suggest a promising nondopaminergic pharmacological strategy for the treatment of dyskinesia in PD. © 2016 International Parkinson and Movement Disorder Society.</AbstractText>
<CopyrightInformation>© 2016 International Parkinson and Movement Disorder Society.</CopyrightInformation>
</Abstract>
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<LastName>Pinna</LastName>
<ForeName>Annalisa</ForeName>
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</AffiliationInfo>
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<LastName>Ko</LastName>
<ForeName>Wai Kin D</ForeName>
<Initials>WK</Initials>
<AffiliationInfo>
<Affiliation>Motac Neuroscience Ltd, Manchester, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute of Laboratory Animal Sciences, China Academy of Medical Sciences, Beijing, China.</Affiliation>
</AffiliationInfo>
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<LastName>Costa</LastName>
<ForeName>Giulia</ForeName>
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<Affiliation>Department of Biomedical Sciences, section of Neuropsychopharmacology, University of Cagliari, Cagliari, Italy.</Affiliation>
</AffiliationInfo>
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<ForeName>Elisabetta</ForeName>
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</AffiliationInfo>
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</AffiliationInfo>
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<Initials>N</Initials>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute of Laboratory Animal Sciences, China Academy of Medical Sciences, Beijing, China.</Affiliation>
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<ForeName>Mojgan Aghazadeh</ForeName>
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<Affiliation>Department of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy.</Affiliation>
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<Affiliation>Motac Neuroscience Ltd, Manchester, UK.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute of Laboratory Animal Sciences, China Academy of Medical Sciences, Beijing, China.</Affiliation>
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<AffiliationInfo>
<Affiliation>Université de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.</Affiliation>
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<AffiliationInfo>
<Affiliation>CNRS, Institut des Maladies Neurodégénératives, Bordeaux, France.</Affiliation>
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<LastName>Carta</LastName>
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<Affiliation>Department of Biomedical Sciences, section of Physiology, University of Cagliari, Cagliari, Italy.</Affiliation>
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</Author>
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<LastName>Morelli</LastName>
<ForeName>Micaela</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>National Research Council of Italy, Neuroscience Institute, Cagliari, Italy.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Biomedical Sciences, section of Neuropsychopharmacology, University of Cagliari, Cagliari, Italy.</Affiliation>
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</Author>
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<Month>02</Month>
<Day>12</Day>
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<Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
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<MeshHeading>
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<QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName>
<QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008252" MajorTopicYN="N">Macaca fascicularis</DescriptorName>
</MeshHeading>
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<MeshHeading>
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<MeshHeading>
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<MeshHeading>
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</MeshHeading>
<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D017207" MajorTopicYN="N">Rats, Sprague-Dawley</DescriptorName>
</MeshHeading>
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</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">adenosine A2A receptor antagonist</Keyword>
<Keyword MajorTopicYN="N">dyskinesia</Keyword>
<Keyword MajorTopicYN="N">non-human primate</Keyword>
<Keyword MajorTopicYN="N">rodent</Keyword>
<Keyword MajorTopicYN="N">serotonin 5-HT1A/1B receptor agonist</Keyword>
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<PubMedPubDate PubStatus="revised">
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<Month>09</Month>
<Day>28</Day>
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<Month>2</Month>
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<ArticleId IdType="doi">10.1002/mds.26475</ArticleId>
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<list>
<country>
<li>Italie</li>
<li>Royaume-Uni</li>
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<li>Angleterre</li>
<li>Grand Manchester</li>
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<li>Manchester</li>
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<name sortKey="Costa, Giulia" sort="Costa, Giulia" uniqKey="Costa G" first="Giulia" last="Costa">Giulia Costa</name>
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<name sortKey="Simola, Nicola" sort="Simola, Nicola" uniqKey="Simola N" first="Nicola" last="Simola">Nicola Simola</name>
<name sortKey="Tabrizi, Mojgan Aghazadeh" sort="Tabrizi, Mojgan Aghazadeh" uniqKey="Tabrizi M" first="Mojgan Aghazadeh" last="Tabrizi">Mojgan Aghazadeh Tabrizi</name>
<name sortKey="Tronci, Elisabetta" sort="Tronci, Elisabetta" uniqKey="Tronci E" first="Elisabetta" last="Tronci">Elisabetta Tronci</name>
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<name sortKey="Ko, Wai Kin D" sort="Ko, Wai Kin D" uniqKey="Ko W" first="Wai Kin D" last="Ko">Wai Kin D. Ko</name>
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<name sortKey="Bezard, Erwan" sort="Bezard, Erwan" uniqKey="Bezard E" first="Erwan" last="Bezard">Erwan Bezard</name>
<name sortKey="Li, Qin" sort="Li, Qin" uniqKey="Li Q" first="Qin" last="Li">Qin Li</name>
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