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Antagonist thioxanthenes

The differential clinical actions of DA blockers on the DA receptor subtypes have not been defined with precision. Most neuroleptics appear to act at both D-1 and D-2 receptors. Some differences exist, however. The thioxanthenes bind to sites related to both DA receptor subtypes, but the butyrophenones seem to prefer sites assocaited with D-2 receptors, binding only weakly to those identified with D-1 receptors. Sulpiride, molindone and metoclopramide are relatively selective D-2 antagonists. [Pg.150]

Conventional antipsychotic (neuroleptic, thioxanthene, dopamine 2 antagonist)... [Pg.181]

Dopamine-receptor antagonists having antipsychotic properties, such as phenothiazine, butyrophenone, and thioxanthene derivatives, and Gl-stimulant drugs, such as metoclopramide, are contraindicated with pergolide. The... [Pg.561]

Phenothiazines, butyrophenones, diphenylbutylpiperidines and thioxanthenes can oppose the effects of levodopa because of their dopamine antagonist properties, causing deterioration of motor function in Parkinson s disease. The antipsychotic effects and ex-trapyramidal adverse effects of these drugs can be opposed by levodopa. Of the atypical antipsychotics, risperidone and olanzapine cause deterioration in motor function in Parkinson s disease. Ziprasidone may act similarly, and there have been reports with quetiapine. Clozapine does not have this effect. [Pg.683]


See other pages where Antagonist thioxanthenes is mentioned: [Pg.359]    [Pg.144]    [Pg.354]    [Pg.1320]    [Pg.359]    [Pg.15]    [Pg.25]    [Pg.28]    [Pg.251]    [Pg.923]    [Pg.924]    [Pg.260]    [Pg.259]    [Pg.47]    [Pg.359]    [Pg.683]    [Pg.791]    [Pg.791]    [Pg.793]   
See also in sourсe #XX -- [ Pg.24 ]




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