Premium
Effects of D 2 dopamine receptor antagonists on fos protein expression in the striatal complex and entorhinal cortex of the nonhuman primate
Author(s) -
Deutch Ariel Y.,
Lewis David A.,
Whitehead Richard E.,
Elsworth J.D.,
Iadarola Michael J.,
Redmond D. Eugene,
Roth Robert H.
Publication year - 1996
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/(sici)1098-2396(199607)23:3<182::aid-syn7>3.0.co;2-4
Subject(s) - nucleus accumbens , haloperidol , dopamine receptor d2 , striatum , dopamine , entorhinal cortex , neuroscience , chemistry , pharmacology , medicine , endocrinology , biology , hippocampus
Recent studies have reported that acute administration of dopamine D 2 receptor antagonists increases expression of the immediate early gene c‐ fos in the rat striatal complex. There have been no corresponding studies of the effects of D 2 antagonists in primate species. Since all clinically effective antipsychotic drugs share D 2 receptor antagonism, it is important to define the extent to which these drugs may alter expression of c‐ fos or its protein product, Fos, in primates. We therefore examined the effects of administration of two D 2 receptor antagonists, haloperidol and metoclopramide, on Fos expression in the striatum and temporal cortices of the vervet monkey. Metoclopramide does not appear to possess significant antipsychotic efficacy but potently produces extrapyramidal side effects, while haloperidol is an effective antipsychotic drug that produces extrapyramidal side effects. Both drugs increased the number of Fos‐like immunoreactive (Fos‐li) neurons in the caudate nucleus and putamen; the numbers of Fos‐li neurons in these regions were increased in both the patch and matrix compartments. Haloperidol but not metoclopramide increased the number of Fos‐li neurons in the nucleus accumbens shell. Similarly, haloperidol but not metoclopramide increased the number of Fos‐li neurons in the entorhinal cortex. Neither drug altered Fos expression in the inferior temporal cortex. These data suggest that the dorsolateral caudate nucleus and putamen may be sites at which D 2 receptor antagonists elicit extrapyramidal side effects, and the nucleus accumbens shell and entorhinal cortex may be loci at which the therapeutic actions of antipsychotic drugs are manifested. © 1996 Wiley‐Liss, Inc.