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Evaluation of risperidone in the neonatal 6-hydroxydopamine model of Lesch-Nyhan syndrome.

Abstract
Rats were treated as neonates with 6-hydroxydopamine (6-OHDA) 100 mg free base in 10 microl intracisternally. Upon maturation, animals were injected with L-dopa and placed in photocell cages for monitoring of locomotion, stereotypies, and self-mutilation. Pretreatment with either risperidone or SCH-23390 significantly reduced locomotion and stereotypies. SCH-23390 eliminated L-dopa induced self-mutilation in all subjects, while risperidone eliminated self-mutilation in all but one subject.
AuthorsS M Allen, J N Freeman, W M Davis
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 59 Issue 2 Pg. 327-30 (Feb 1998) ISSN: 0091-3057 [Print] United States
PMID9476977 (Publication Type: Journal Article)
Chemical References
  • Benzazepines
  • Dopamine Agents
  • Dopamine Antagonists
  • Sympatholytics
  • Levodopa
  • Oxidopamine
  • Risperidone
Topics
  • Animals
  • Animals, Newborn
  • Behavior, Animal (drug effects)
  • Benzazepines (pharmacology)
  • Disease Models, Animal
  • Dopamine Agents (pharmacology)
  • Dopamine Antagonists (therapeutic use)
  • Dose-Response Relationship, Drug
  • Female
  • Lesch-Nyhan Syndrome (chemically induced, drug therapy, psychology)
  • Levodopa (pharmacology)
  • Male
  • Motor Activity (drug effects)
  • Oxidopamine (toxicity)
  • Rats
  • Rats, Sprague-Dawley
  • Risperidone (therapeutic use)
  • Self Mutilation (drug therapy, psychology)
  • Sympatholytics (toxicity)

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