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
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.