A simple rodent assay for the in vivo identification of agents with potential to reduce levodopa-induced dyskinesia in Parkinson's disease

被引:28
作者
Johnston, TH
Lee, J
Gomez-Ramirez, J
Fox, SH
Brotchie, JM
机构
[1] Toronto Western Hosp, Toronto Western Res Inst, Movement Disorders Clin, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Div Neurol, Toronto, ON, Canada
[3] Univ Hlth Network, Toronto Western Hosp, Toronto Western Res Inst, Toronto, ON, Canada
[4] Atuka Ltd, Toronto, ON, Canada
关键词
Parkinson's disease; dyskinesia; rat; L-DOPA; therapeutics;
D O I
10.1016/j.expneurol.2004.10.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
L-DOPA-induced dyskinesia (LID) remains a major complication of the treatment of Parkinson's disease (PD). Whilst the MPTP-lesioned primate provides an excellent animal model in which to develop new therapies, however, it is logistically difficult to employ widely, Thus, a simple rodent assay to screen multiple compounds as candidates for further study of their potential in LID would be a valuable addition to the drug development process. Here, we investigate how agents with demonstrated ability to reduce LID in man and monkey can regulate L-DOPA-induced behaviours in the reserpine-treated rat. Administration Of L-DOPA (125 mg/kg) to reserpine-treated rats elicited high levels of both horizontal and vertical movement. Drugs that have previously been found to reduce LID in parkinsonian primates and PD patients without compromising the anti-parkinsonian efficacy Of L-DOPA selectively and dose-dependently reduce vertical components of activity when co-administered with L-DOPA in the reserpine-treated rat. For instance, amantadine (1 mg/kg) and idazoxan (3 mg/kg) reduced vertical activity by 59% and 83%, respectively, while neither drug had significant effects on horizontal activity. In contrast, haloperidol (1 mg/kg), an agent lacking the ability to selectively reduce LID without compromising the antiparkinsonian actions Of L-DOPA, reduced both horizontal and vertical activity, by 98% and 99%, respectively. We also assessed the actions of an NMDA antagonist, a class of compound proposed to have potential as anti-dyskinetic agents. The effects of MK-801 were dose-dependent (0.01-0.5 mg/kg), at some doses (e.g., 0.05 mg/kg), providing selective reduction of vertical activity (90%), at others (e.g., 0.5 mg/kg), non-selective reduction of vertical and horizontal (99% and 77%, respectively). These observations highlight the association between potential anti-dyskinetic action and a selective reduction in L-DOPA-induced vertical activity in the reserpine-treated rat. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:243 / 250
页数:8
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