Spontaneous orofacial dyskinesias in a captive cynomolgus monkey: implications for tardive dyskinesia.
Identifieur interne : 004E76 ( PubMed/Checkpoint ); précédent : 004E75; suivant : 004E77Spontaneous orofacial dyskinesias in a captive cynomolgus monkey: implications for tardive dyskinesia.
Auteurs : N M Rupniak [Royaume-Uni] ; S J Tye ; M J Steventon ; S. Boyce ; S D IversenSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1990.
English descriptors
- KwdEn :
- Animals, Benzazepines (pharmacology), Disease Models, Animal, Dose-Response Relationship, Drug, Dyskinesia, Drug-Induced (physiopathology), Facial Expression, Facial Muscles (physiopathology), Haloperidol (pharmacology), Macaca fascicularis (physiology), Mastication (physiology), Movement Disorders (physiopathology), Physostigmine (pharmacology), Scopolamine Hydrobromide (pharmacology), Stereotyped Behavior (physiology).
- MESH :
- chemical , pharmacology : Benzazepines, Haloperidol, Physostigmine, Scopolamine Hydrobromide.
- physiology : Macaca fascicularis, Mastication, Stereotyped Behavior.
- physiopathology : Dyskinesia, Drug-Induced, Facial Muscles, Movement Disorders.
- Animals, Disease Models, Animal, Dose-Response Relationship, Drug, Facial Expression.
Abstract
We describe a syndrome of spontaneous orofacial dyskinesias and cage stereotypies in a singly housed adult cynomolgus monkey never previously exposed to neuroleptic drugs. Abnormal movements were readily suppressed by acute treatment with haloperidol (0.03-0.24 mg/kg i.m.) or SCH23390 (0.05-0.2 mg/kg i.m.) but not by physostigmine (0.005-0.04 mg/kg i.m.) or scopolamine (0.0025-0.04 mg/kg i.m.). The symptomatology and response to pharmacological manipulations was indistinguishable from that previously attributed to chronic neuroleptic treatment in primates. Our findings indicate that neuroleptic-induced tardive dyskinesias in most primate studies have not been clearly demonstrated.
DOI: 10.1002/mds.870050410
PubMed: 2259355
Affiliations:
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pubmed:2259355Le document en format XML
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<author><name sortKey="Rupniak, N M" sort="Rupniak, N M" uniqKey="Rupniak N" first="N M" last="Rupniak">N M Rupniak</name>
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<author><name sortKey="Steventon, M J" sort="Steventon, M J" uniqKey="Steventon M" first="M J" last="Steventon">M J Steventon</name>
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<author><name sortKey="Boyce, S" sort="Boyce, S" uniqKey="Boyce S" first="S" last="Boyce">S. Boyce</name>
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<term>Dyskinesia, Drug-Induced (physiopathology)</term>
<term>Facial Expression</term>
<term>Facial Muscles (physiopathology)</term>
<term>Haloperidol (pharmacology)</term>
<term>Macaca fascicularis (physiology)</term>
<term>Mastication (physiology)</term>
<term>Movement Disorders (physiopathology)</term>
<term>Physostigmine (pharmacology)</term>
<term>Scopolamine Hydrobromide (pharmacology)</term>
<term>Stereotyped Behavior (physiology)</term>
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<front><div type="abstract" xml:lang="en">We describe a syndrome of spontaneous orofacial dyskinesias and cage stereotypies in a singly housed adult cynomolgus monkey never previously exposed to neuroleptic drugs. Abnormal movements were readily suppressed by acute treatment with haloperidol (0.03-0.24 mg/kg i.m.) or SCH23390 (0.05-0.2 mg/kg i.m.) but not by physostigmine (0.005-0.04 mg/kg i.m.) or scopolamine (0.0025-0.04 mg/kg i.m.). The symptomatology and response to pharmacological manipulations was indistinguishable from that previously attributed to chronic neuroleptic treatment in primates. Our findings indicate that neuroleptic-induced tardive dyskinesias in most primate studies have not been clearly demonstrated.</div>
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<ArticleTitle>Spontaneous orofacial dyskinesias in a captive cynomolgus monkey: implications for tardive dyskinesia.</ArticleTitle>
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<Abstract><AbstractText>We describe a syndrome of spontaneous orofacial dyskinesias and cage stereotypies in a singly housed adult cynomolgus monkey never previously exposed to neuroleptic drugs. Abnormal movements were readily suppressed by acute treatment with haloperidol (0.03-0.24 mg/kg i.m.) or SCH23390 (0.05-0.2 mg/kg i.m.) but not by physostigmine (0.005-0.04 mg/kg i.m.) or scopolamine (0.0025-0.04 mg/kg i.m.). The symptomatology and response to pharmacological manipulations was indistinguishable from that previously attributed to chronic neuroleptic treatment in primates. Our findings indicate that neuroleptic-induced tardive dyskinesias in most primate studies have not been clearly demonstrated.</AbstractText>
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