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• W2132151012 abstract "It has been suggested that the favorable side-effect profiles of atypical antipsychotics (e.g. clozapine and amisulpride) are related to their ∼100-fold faster dissociation from dopamine D2 receptors (D2R) compared with typical antipsychotics (e.g. haloperidol and chlorpromazine). Fast dissociation would entail rapidly reversible antagonism; however, this has not been thoroughly studied using functional assays. We compared the reversibilities of D2R antagonism by 17 compounds using an electrophysiological method to measure dopamine-evoked potassium channel activation via D2R. Varying rates and amplitudes of D2R response recovery were observed following antagonist removal. Whereas recovery rates differed 15-fold between atypical drugs, recovery from clozapine and amisulpride antagonism was, unexpectedly, less than twofold faster than from chlorpromazine. The recovery amplitude correlated with calculated water solubility and lipid/water distribution coefficients, suggesting variable drug partitioning into cell membranes. Our data do not support the notion that the rate of reversibility of D2R antagonism is what distinguishes atypical from typical antipsychotics." @default.
• W2132151012 created "2016-06-24" @default.
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• W2132151012 date "2013-09-30" @default.
• W2132151012 modified "2023-10-12" @default.
• W2132151012 title "Typical and atypical antipsychotics do not differ markedly in their reversibility of antagonism of the dopamine D2 receptor" @default.
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• W2132151012 doi "https://doi.org/10.1017/s1461145713000801" @default.
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