Treatment of Tourette's Syndrome with RO22–1319, a D-2-Receptor Antagonist
- 11 October 1984
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 311 (15) , 989
- https://doi.org/10.1056/nejm198410113111517
Abstract
To the Editor: Haloperidol is the current treatment of choice for Tourette's syndrome.1 However, the reduction of motor and vocal tics in response to this nonspecific dopamine-receptor blocker is often limited by adverse effects, which can prevent treatment with a dosage adequate for symptom control or lead to noncompliance. The extrapyramidal side effects of haloperidol are assumed to result from nigrostriatal dopamine-receptor blockade.1 RO22–1319, representing a new class of drugs designed for three-dimensional computer models of receptors, is a novel dopamine-receptor antagonist.2 It is a water-soluble pyrroloisoquinoline derivative, whose chemical structure is different from that of other antipsychotic agents (rac. . . .Keywords
This publication has 2 references indexed in Scilit:
- Pharmacological effects of Ro 22-1319: A new antipsychotic agentPsychopharmacology, 1983
- Dopamine receptor model and its application in the design of a new class of rigid pyrrolo[2,3-g]isoquinoline antipsychoticsJournal of Medicinal Chemistry, 1981