TY - JOUR
T1 - "Classical" and "atypical" antipsychotic drugs
T2 - Differential antagonism of amphetamine- and apomorphine-induced alterations of spontaneous neuronal activity in the neostriatum and nucleus accumbens
AU - Rebec, George V.
AU - Bashore, Theodore R.
AU - Zimmerman, Kenneth S.
AU - Alloway, Kevin
N1 - Funding Information:
This research was supported, in part, by a biomedical research support grant from Indiana University and by USPHS Grant DA-02451 awarded to GVR. The authors wish to thank Karen Brugge for her assistance in conducting some experiments and Suzanne Hull for preparing the illustrations. Sandoz Pharmaceuticals (East Hanover, N J) provided a generous supply of clozapine.
PY - 1979/11
Y1 - 1979/11
N2 - The ability of clozapine and haloperidol to antagonize the depression of firing rate produced by d-amphetamine and apomorphine in the neostriatum and nucleus accumbens was tested in immobilized, locally anesthetized rats. In the neostriatum, an intraperitoneal injection of 2.5 mg/kg d-amphetamine or 1.0 mg/kg apomorphine produced a prolonged inhibition of neuronal activity that was reversed by a subsequent injection of either 20 mg/kg clozapine or 2.0 mg/kg haloperidol. An analysis of the onset and magnitude of the blockade revealed that clozapine was more effective than haloperidol in reversing the amphetamine response but that both antipsychotic drugs produced a comparable blockade of the apomorphine-induced depression. Similar results were obtained in the nucleus accumbens. The data indicate that although clozapine acts equieffectively in the neostriatum and nucleus accumbens, this atypical antipsychotic drug, aside from blocking postsynaptic dopamine receptors, may exert at least some of its effects by preventing dopamine release.
AB - The ability of clozapine and haloperidol to antagonize the depression of firing rate produced by d-amphetamine and apomorphine in the neostriatum and nucleus accumbens was tested in immobilized, locally anesthetized rats. In the neostriatum, an intraperitoneal injection of 2.5 mg/kg d-amphetamine or 1.0 mg/kg apomorphine produced a prolonged inhibition of neuronal activity that was reversed by a subsequent injection of either 20 mg/kg clozapine or 2.0 mg/kg haloperidol. An analysis of the onset and magnitude of the blockade revealed that clozapine was more effective than haloperidol in reversing the amphetamine response but that both antipsychotic drugs produced a comparable blockade of the apomorphine-induced depression. Similar results were obtained in the nucleus accumbens. The data indicate that although clozapine acts equieffectively in the neostriatum and nucleus accumbens, this atypical antipsychotic drug, aside from blocking postsynaptic dopamine receptors, may exert at least some of its effects by preventing dopamine release.
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U2 - 10.1016/0091-3057(79)90036-4
DO - 10.1016/0091-3057(79)90036-4
M3 - Article
C2 - 43515
AN - SCOPUS:0018630558
SN - 0091-3057
VL - 11
SP - 529
EP - 538
JO - Pharmacology Biochemistry and Behavior
JF - Pharmacology Biochemistry and Behavior
IS - 5
ER -