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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Levetiracetam Potentiates the Antidyskinetic Action of Amantadine in the 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-Lesioned Primate Model of Parkinson's Disease
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Levetiracetam Potentiates the Antidyskinetic Action of Amantadine in the 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-Lesioned Primate Model of Parkinson's Disease

机译:左乙拉西坦增强金刚烷胺在1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)致帕金森病灵长类动物模型中的抗运动障碍作用

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摘要

Levetiracetam (LEV) (Keppra;UCB Pharma,Brussels,Belgium) has recently been reported to have antidyskinetic activity against levodopa (L-DOPA)-induced dyskinesia in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-lesioned marmoset and macaque models of Parkinson's disease.Amantadine is frequently used as adjunctive therapy for L-DOPA-induced dyskinesia,but adverse effects limit its clinical utility.The current study was designed to investigate whether LEV can potentiate the antidyskinetic action of amantadine.The antiparkinsonian and antidyskinetic effects of LEV (13 and 60 mg/kg) and amantadine (0.01,0.03,0.1,and 0.3 mg/kg),administered alone and in combination,were assessed in the MPTP-lesioned marmoset model of L-DOPA-induced dyskinesia (n=12).LEV (60 mg/kg) and amantadine (0.3 mg/kg) administered alone significantly reduced L-DOPA-induced dyskinesia without compromising the antiparkinsonian action of L-DOPA.Lower doses were without any significant effects.The combination of LEV (60 mg/kg) and amantadine (0.01,0.03,0.1,and 0.3 mg/kg) significantly decreased dyskinesia severity,without compromising the antiparkinsonian action of L-DOPA,more efficaciously than LEV or amantadine monotherapy.These results support the concept that normalization of different pathophysiological mechanisms (i.e.,altered synchronization between neurons and enhanced N-methyl-D-aspartate transmission) has a greater efficacy.Combined LEV/amantadine therapy might be useful as an adjunct to L-DOPA to treat dyskinetic side effects and to expand the population of Parkinson's disease patients who benefit from treatment with amantadine alone.
机译:左乙拉西坦(LEV)(Keppra; UCB Pharma,Brussels,Belgium)最近被报道具有抗左旋多巴(L-DOPA)引起的运动障碍的运动障碍活性,该运动障碍是由1-methyl-4-phenyl-1,2,3,6-四氢吡啶(MPTP)损伤的mar猴和帕金森氏病的猕猴模型。金刚烷胺经常用作L-DOPA诱导的运动障碍的辅助治疗,但不良反应限制了其临床实用性。本研究旨在研究LEV是否可以增强抗运动性在MPTP损伤的mo猴模型中评估了LEV(13和60 mg / kg)和金刚烷胺(0.01、0.03、0.1和0.3 mg / kg)单独或组合给药的抗帕金森病和抗运动障碍作用L-DOPA引起的运动障碍(n = 12)。单独服用LEV(60 mg / kg)和金刚烷胺(0.3 mg / kg)可以显着减轻L-DOPA引起的运动障碍,而不会损害L-DOPA的抗帕金森病作用。没有任何明显的影响。 LEV(60 mg / kg)和金刚烷胺(0.01、0.03、0.1和0.3 mg / kg)显着降低了运动障碍的严重程度,而没有损害L-DOPA的抗帕金森病作用,比LEV或金刚烷胺单一疗法更有效。这些结果支持了这一概念。不同病理生理机制的正常化(即神经元之间同步性的改变和N-甲基-D-天冬氨酸的传递增强)具有更高的疗效。LEV /金刚烷胺联合治疗可能是L-DOPA的辅助治疗运动障碍性副作用和扩大仅从金刚烷胺治疗中受益的帕金森氏病患者的人数。

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