Progress in Neuro-Psychopharmacology and Biological Psychiatry 1990-01-01

Evidence that lack of brain dopamine during development can increase the susceptibility for aggression and self-injurious behavior by influencing D1-dopamine receptor function.

G R Breese, H E Criswell, R A Mueller

Index: Prog. Neuropsychopharmacol. Biol. Psychiatry 14 Suppl , S65-80, (1990)

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Abstract

1. Lesch-Nyhan disease has a defined neurological lesion that is accompanied by abnormal motor function, aggression and self-injurious behavior. 2. The dopamine deficiency in Lesch-Nyhan disease has been modelled by destroying dopamine-containing neurons in neonatal rats with 6-hydroxydopamine. 3. Because D1-dopamine antagonists will block self-injurious behavior induced by L-DOPA in neonatal-6-OHDA-lesioned rats, D1-dopamine antagonists are proposed as a potential therapy for aggression and self-injurious behavior in patients with these symptoms. 4. The determination that the drug SCH-12679, which exhibited effectiveness against aggressiveness in mentally retarded patients, is a D1-dopamine antagonist supports the view that new D1-dopamine antagonists being developed will be an effective therapy for some types of aberrant behavior in this population.

Related Compounds

Structure Name/CAS No. Articles
SCH-12679 MALEATE Structure SCH-12679 MALEATE
CAS:39624-66-3