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J Pharmacol Exp Ther 1999 Aug;290(2):731-9

Nicotinic acetylcholine receptor agonist SIB-1508Y improves cognitive
functioning in chronic low-dose MPTP-treated monkeys.

Schneider JS, Tinker JP, Van Velson M, Menzaghi F, Lloyd GK
Department of Pathology, Anatomy, and Cell Biology, Thomas Jefferson
University, Philadelphia, Pennsylvania.

Monkeys that receive chronic low-dose 1-methyl-4-phenyl-1,2,3,
6-tetrahydropyridine (MPTP) administration have difficulty performing
numerous cognitive tasks. This study further examines the extent to which
chronic low-dose MPTP exposure affects performance of a visual memory task
[variable delayed response (VDR)] with both attentional and short-term
memory components and assesses the effects of the novel neuronal nicotinic
acetylcholine receptor agonist SIB-1508Y and levodopa on cognitive task
performance. Before MPTP treatment, these monkeys displayed a
delay-dependent decrement in performance on the VDR task and performed well
on delayed matching-to-sample and visual pattern discrimination tasks.
Chronic low-dose MPTP treatment caused a shift to a delay-independent
pattern of responding on the VDR task, such that short-delay trials were
performed as poorly as long-delay trials. There were also deficits in
performing the delayed matching-to-sample task, whereas visual
discrimination performance remained intact. SIB-1508Y normalized the pattern
of response on the VDR task by significantly improving performance on
short-delay trials and on the delayed matching-to-sample task. These effects
lasted up to 24 to 48 h after SIB-1508Y administration. Neither levodopa nor
nicotine significantly improved task performance. These results suggest that
chronic low-dose MPTP exposure results in a cognitive disturbance that can
be corrected by the nicotinic acetylcholine receptor agonist SIB-1508Y but
not by levodopa. Thus, SIB-1508Y may be useful in the treatment of the
cognitive deficits in Parkinson's disease.

PMID: 10411585, UI: 99340176
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