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NOP RECEPTOR AGONISTS FOR THE TREATMENT OF L-DOPA INDUCED DYSKINESIAS

机译:NOP受体激动剂用于治疗L-多巴诱发的运动障碍

摘要

The present invention relates to the chronic treatment with L,3-4-dihydroxyphenylalanine (L-DOPA). Chronic L-DOPA administration still represents the most effective pharmacological therapy of Parkinson's disease (PD) although it is invariably associated with the appearance (within 5-10 years after start of the therapy, in about 80 % of patients) of motor complications that limit its clinical effectiveness and greatly reduce the quality of life of patients (Obeso et al., 2000). These motor complications encompass motor fluctuations (e.g. wearing off and 'on-off fluctuations) and abnormal involuntary movements or dyskinesias (peak dose and diphasic dyskinesias, dystonia). We report for the first time that in an animal model of dyskinesias, administration of agonists at nociceptin/orphanin FQ receptors, termed NOP receptors, dramatically reduces abnormal involuntary movements induced by L-DOPA administration. NOP receptor agonists thus represent a novel class of drugs useful for the treatment of L-DOPA induced dyskinesias.
机译:本发明涉及用L,3-4-二羟基苯丙氨酸(L-DOPA)的慢性治疗。长期服用L-DOPA仍代表帕金森氏病(PD)的最有效药理疗法,尽管它总是与运动并发症的出现(在治疗开始后5-10年内,约80%的患者)相关,但这种局限性它的临床有效性大大降低了患者的生活质量(Obeso等,2000)。这些运动并发症包括运动波动(例如磨损和'on-off波动)和异常的不自主运动或运动障碍(峰值剂量和两相运动障碍,肌张力障碍)。我们首次报道,在运动障碍的动物模型中,对伤害性感受器/孤啡肽FQ受体(称为NOP受体)的激动剂的施用显着减少了由L-DOPA施用引起的异常不自主运动。因此,NOP受体激动剂代表了用于治疗L-DOPA诱导的运动障碍的新型药物。

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