Title of Chapter/Section
Translational Value of Drug Discrimination with Typical and Atypical Antipsychotic Drugs
Title of Book
The Behavioural Neuroscience of Drug Discrimination
Editor(s) of Book
Joseph H. Porter, Adam J. Prus
Place of Publication
Springer International Publishing AG
Year of Publication
Series (if applicable)
Current Topics in Behavioral Neurosciences
This chapter focuses on the translational value of drug discrimination as a preclinical assay for drug development. In particular, the importance of two factors, i.e., training dose and species, for drug discrimination studies with the atypical antipsychotic clozapine is examined. Serotonin receptors appear to be an important pharmacological mechanism mediating clozapine’s discriminative cue in both rats and mice, although differences are clearly evident as antagonism of cholinergic muscarinic receptors is important in rats at a higher training dose (5.0 mg/kg) of clozapine, but not at a lower training dose (1.25 mg/kg). Antagonism of α1 adrenoceptors is a sufficient mechanism in C57BL/6 and 129S2 mice to mimic clozapine’s cue, but not in DBA/2 and B6129S mice, and only produces partial substitution in low-dose clozapine discrimination in rats. Dopamine antagonism produces partial substitution for clozapine in DBA/2, 129S2, and B6129S mice, but not in C57BL/6 mice, and partial substitution is seen with D4 antagonism in low-dose clozapine drug discrimination in rats. Thus, it is evident that clozapine has a complex mixture of receptor contributions towards its discriminative cue based on the data from the four mouse strains that have been tested that is similar to the results from rat studies. A further examination of antipsychotic stimulus properties in humans, particularly in patients with schizophrenia, would go far in evaluating the translational value of the drug discrimination paradigm for antipsychotic drugs.
Prus, Joseph H.; Webster, Kevin; and Prus, Adam J., "Translational Value of Drug Discrimination with Typical and Atypical Antipsychotic Drugs" (2017). Book Sections/Chapters. 57.