Acute exposure to kainic acid (KA) induces neurochemical changes in do
paminergic systems in the brain and the aim of the present study was t
o investigate the acute toxicity of KA upon dopamine D-2 receptors. Ad
ult rats were injected intraperitoneally with either saline or 16 mg/k
g KA. Brains were removed after 4 h. Membrane homogenates were prepare
d from seven brain regions and in addition, frozen coronal sections we
re sectioned for comparative quantitative autoradiographic analysis. D
opamine D-2 receptors were characterised by saturation studies using [
I-125]iodosulpiride, [H-3]raclopride and [H-3]spiperone. KA produced a
2-fold decrease in receptor affinity for [I-125]iodosulpiride and a 2
-fold increase in receptor density in all regions studied except stria
tum. Quantitative autoradiography with [I-125]iodosulpiride showed sim
ilar increases in D-2 labelling following KA except in caudate putamen
, nucleus accumbens and olfactory tubercle. In contrast, there was no
change in [H-3]spiperone binding in whole brain minus striatum nor in
striatum alone after KA treatment. KA produced a significant increase
in B-max for [H-3]raclopride in whole brain minus striatum and in stri
atum alone with minimal changes in affinity. These findings demonstrat
e acute changes in rat brain dopamine D-2 receptors labelled with [I-1
25]iodosulpiride and [H-3]raclopride but not [H-3]spiperone after ECA
treatment predominantly in extra striatal regions. (C) 1998 Elsevier S
cience Ireland Ltd. All rights reserved.