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The opiate antagonist naloxone suppresses a rodent model of tardive dyskinesia

✍ Scribed by Dr. A. Jon Stoessl; Elizabeth Polanski; Hanna Frydryszak


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
778 KB
Volume
8
Category
Article
ISSN
0885-3185

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✦ Synopsis


Abstract

The effects of both opiate agonists and the opiate antagonist naloxone were examined in a rodent model of tardive dyskinesia (TD). Chronic (˜20 weeks) administration of fluphenazine resulted in the emergence of vacuous chewing mouth movements (VCMs), a response which may be a useful model for this disorder. Fluphenazine‐induced VCMs were not affected by a variety of selective opiate agonists administered intracerebroventricularly, but were potently suppressed by subcutaneous administration of the opiate antagonist naloxone. These findings suggest that increased opiate transmission may contribute to the pathogenesis of TD. Further investigation of the role of opiate antagonists in treating this disorder are warranted.


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The effects of bilateral excitotoxic lesions of the subthalamic nucleus on vacuous chewing movements induced by chronic neuroleptic therapy were examined in the rat. Fluphenazine decanoate (25 mg/kgi.m. q 3 weeks X 24 weeks) inducedvacuous chewing movements, as previously described. This response wa