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Vol. 288, Issue 3, 1093-1100, March 1999
prah,
ivin and
an
Sket
University of Ljubljana, School of Medicine, Institute of
Pathophysiology, Ljubljana, Slovenia
LEK-8829
[9,10-didehydro-N-methyl-(2-propynyl)-6-methyl-8-aminomethylergoline
bimaleinate] is an antagonist of dopamine D2 receptors and
serotonin (5-HT)2 and 5-HT1A receptors in
intact animals and a D1 receptor agonist in
dopamine-depleted animals. In the present study, we used rats with
unilateral striatal lesions with ibotenic acid (IA) to investigate the
dopamine receptor activities of LEK-8829 in a model with innervated
dopamine receptors. The IA-lesioned rats circled ipsilaterally when
challenged with apomorphine, the mixed agonist on
D1/D2 receptors. LEK-8829 induced a
dose-dependent contralateral turning that was blocked by D1
receptor antagonist SCH-23390. The treatment with D1
receptor agonist SKF-82958 induced ipsilateral turning, whereas the
treatment with D2 receptor antagonist haloperidol induced
contralateral posture. The combined treatment with SKF-82958 and
haloperidol resulted in a weak contralateral turning, indicating the
possible receptor mechanism of contralateral turning induced by
LEK-8829. Bromocriptine induced a weak ipsilateral turning that
was blocked by haloperidol. The ipsilateral turning induced by
bromocriptine was significantly potentiated by the coadministration of
a low dose but not by a high dose of LEK-8829. The potentiation of
turning was blocked either by SCH-23390 or by haloperidol. The
potentiation of ipsilateral turning suggests the costimulation of
D2 and D1 receptors by bromocriptine and LEK-8829, respectively, whereas the lack of potentiation by the highest
dose of LEK-8829 may be explained by the opposing activity of LEK-8829
and bromocriptine at D2 receptors. We propose that the
D2 and 5HT2 receptor-blocking and
D1 receptor-stimulating profile of LEK-8829 is promising
for the treatment of negative symptoms of schizophrenia.
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