首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effects of L-tryptophan on L-DOPA-induced dyskinesia in the 1-methyl-4-phenyl-1 ,2,3,6-tetrahydropyridine (MPTP)-treated macaque model of Parkinson's disease
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Effects of L-tryptophan on L-DOPA-induced dyskinesia in the 1-methyl-4-phenyl-1 ,2,3,6-tetrahydropyridine (MPTP)-treated macaque model of Parkinson's disease

机译:L-色氨酸对帕金森病的1-甲基-4-苯基-1,2,9-四氢吡啶(MPTP)猕猴(MPTP)猕猴(MPTP)猕猴(MPTP)猕猴(MPTP)猕猴(MPTP)的影响

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摘要

In animal models of Parkinson's disease (PD), the serotonergic (5-hydroxytryptamine, 5-HT) system is thought to play an important pathophysiological role in the development and expression of L-3,4-dihydroxyphenylalanine (L-3,4-dihydroxyphenylalanine-DOPA)-induced dyskinesia (LID). These abnormal involuntary movements are associated with the unregulated release of dopamine from 5-HT fibres. Thus, modulating the false neurotransmitter release from 5-HT neurons, via attuning the serotonin tone, may be a potential therapeutic strategy in the treatment of LID. In this study, we investigated the effects of the primary precursor of 5-HT, L-tryptophan, on LID in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated macaques. L-tryptophan treatment (0.5-5.0 g) dramatically abolished the expression of LID. However, this effect was associated with worsening of the therapeutic effects of l-DOPA. These behavioural data further support the role of the serotonergic system in expression of LID, highlighting the difficult challenge of targeting 5-HT neurons for alleviating dyskinesia and maintaining the therapeutic response of l-DOPA.
机译:在帕金森病(Pd)的动物模型中,据认为,血清奈尼(5-羟基 - 羟基胺,5-HT)系统在L-3,4-二羟基苯氨基的发育和表达中发挥着重要的病理生理作用(L-3,4-二羟基苯丙氨酸-DOPA) - 诱导的止吐剂(盖子)。这些异常的非自愿运动与来自5-HT纤维的多巴胺的未调节释放有关。因此,通过调节血清素色调调节5-HT神经元的假神经递质释放,可以是治疗盖子的潜在治疗策略。在这项研究中,我们研究了5-HT,L-色氨酸,盖子在1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP) - 治疗猕猴中的盖子的原发性前体的影响。 L-色氨酸处理(0.5-5.0g)显着废除了盖子的表达。然而,这种效果与L-DOPA的治疗效果恶化有关。这些行为数据进一步支持Serotonergic系统在盖子表达中的作用,突出了靶向5-HT神经元的困难挑战,以减轻止吐剂瘤和维持L-DOPA的治疗反应。

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