Effects of acute and subchronic administration of typical and atypical antipsychotic drugs on the neurotensin system of the rat brain

Citation
B. Kinkead et al., Effects of acute and subchronic administration of typical and atypical antipsychotic drugs on the neurotensin system of the rat brain, J PHARM EXP, 295(1), 2000, pp. 67-73
Citations number
40
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
ISSN journal
00223565 → ACNP
Volume
295
Issue
1
Year of publication
2000
Pages
67 - 73
Database
ISI
SICI code
0022-3565(200010)295:1<67:EOAASA>2.0.ZU;2-U
Abstract
The acute and subchronic effects of a variety of doses of a prototype typic al (haloperidol) or one of several atypical antipsychotic drugs (clozapine, olanzapine, risperidone, quetiapine, or sertindole) on regional brain neur otensin (NT) tissue concentrations, and NT receptor binding were examined. Acute administration of haloperidol, clozapine, olanzapine, and risperidone dose-dependently increased NT tissue concentrations in the nucleus accumbe ns. Haloperidol, olanzapine, risperidone, and sertindole also increased NT tissue concentrations in the caudate nucleus. NT tissue concentrations in t he nucleus accumbens and caudate remained elevated after 14-day administrat ion of haloperidol, olanzapine, sertindole, and risperidone. In contrast, a t the doses studied, quetiapine decreased NT tissue concentrations in the n ucleus accumbens; clozapine had no effect. Haloperidol significantly increa sed NT receptor binding in the substantia nigra after 14-day administration . All of the atypical antipsychotic drugs decreased NT receptor binding in the nucleus accumbens and in the substantia nigra. Although these studies d o not conclusively support the hypothesis that increased NT neurotransmissi on is involved in the clinically relevant effects of all antipsychotic drug s, the extant evidence clearly suggests that further study is warranted. In consistencies in the data suggest that differential effects of antipsychoti c drug administration on subpopulations of NT neurons must be scrutinized f urther.