Abstract
The perphenazine and fluphenazine GABA esters 3 and 4 evaluated in rat models for antipsychotic activity displayed a significant decrease of catalepsy associated with increased prolactin blood levels. Efficacy was evaluated in the d-amphetamine-induced hyperactivity model, where perphenazine abolished hyperactivity and induced sedation and catalepsy, whereas 3 reduced hyperactivity without sedation or catalepsy. Thus, 3 (BL-1020) constitutes a prototype of novel antipsychotics possessing GABAergic activity. A phase II study is in progress.
MeSH terms
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Administration, Oral
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Animals
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Antipsychotic Agents / adverse effects
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Antipsychotic Agents / chemical synthesis*
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Antipsychotic Agents / pharmacology
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Biological Availability
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Catalepsy / chemically induced
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Dextroamphetamine
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Dyskinesia, Drug-Induced / etiology*
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Esters
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Fluphenazine / adverse effects
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Fluphenazine / analogs & derivatives
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Fluphenazine / chemical synthesis
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Fluphenazine / pharmacology
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Male
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Perphenazine / adverse effects
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Perphenazine / analogs & derivatives*
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Perphenazine / chemical synthesis*
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Perphenazine / pharmacology
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Prodrugs / adverse effects
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Prodrugs / chemical synthesis*
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Prodrugs / pharmacology
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Prolactin / metabolism
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Rats
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Rats, Wistar
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Schizophrenia / drug therapy
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gamma-Aminobutyric Acid / adverse effects
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gamma-Aminobutyric Acid / analogs & derivatives*
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gamma-Aminobutyric Acid / chemical synthesis*
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gamma-Aminobutyric Acid / pharmacology
Substances
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Antipsychotic Agents
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Esters
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Prodrugs
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gamma-Aminobutyric Acid
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Prolactin
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Perphenazine
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Fluphenazine
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Dextroamphetamine