Ea. Jones et al., Intrastriatal GABA(A) receptor blockade does not alter dopamine D-1/D-2 receptor interactions in the intact rat striatum, NEUROSCIENC, 102(2), 2001, pp. 381-389
The purpose of this study was to investigate the effects of intrastriatal b
lockade of GABA(A) receptors on dopamine D-1/D-2 receptor interactions in t
he intact rat striatum. Muscarinic receptors mediate the ability of the D-2
receptor antagonist, eticlopride, to block an increase in striatonigral ne
uropeptide messenger RNA stimulated by the full D-1 agonist, SKF-82958. How
ever, because D-2 receptor antagonists activate striatopallidal neurons, it
is possible that increased GABA release from local medium spiny axon colla
terals also contributes to the ability of eticlopride to block the effects
of SKF-82958. This hypothesis was addressed by infusing the GABA(A) recepto
r antagonist, bicuculline, into the dorsal striatum in rats treated with et
iclopride and SKF-82958. In contrast to the actions of the muscarinic antag
onist, scopolamine, bicuculline did not affect the increase in behaviors in
duced by SKF-82958 or the ability of eticlopride to block them. Quantitativ
e in situ hybridization demonstrated that bicuculline did not significantly
affect basal preprodynorphin messenger RNA, nor did it affect the ability
of eticlopride to decrease SKF-82958-induced preprodynorphin messenger RNA.
However, the level of the preprodynorphin hybridization signal in bicucull
ine plus SKF-82958-treated rats was significantly lower than in saline plus
SKF-82958-treated rats. In contrast, bicuculline, eticlopride or SKF-82958
by themselves increased basal preproenkephalin messenger RNA. However, the
re was no significant interaction among bicuculline, eticlopride and SKF-82
958 on preproenkephalin messenger RNA levels.
These data indicate that blockade of striatal GABA(A) receptors has only a
subtle effect on acute dopamine agonist-induced changes in gene expression.
These results are discussed in the context of local intrastriatal interact
ions. (C) 2001 IBRO. Published by Elsevier Science Ltd. All rights reserved
.