Department of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Leioa, Spain; Neurodegenerative Diseases, Biocruces Health Research Institute, Barakaldo, Spain.
Université de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France; Centre National de la Recherche Scientifique, Institut des Maladies Neurodégénératives, UMR 5293, Bordeaux, France.
Int Rev Neurobiol. 2019;146:259-279. doi: 10.1016/bs.irn.2019.06.013. Epub 2019 Jul 18.
Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons in the substantia nigra, the depletion of striatal dopamine and the presence of Lewy aggregates containing alpha-synuclein. Clinically, there are motor impairments involving cardinal movement symptoms, bradykinesia, resting tremor, muscle rigidity, and postural abnormalities, along with non-motor symptoms such as sleep, behavior and mood disorders. The current treatment for PD focuses on restoring dopaminergic neurotransmission by l-3,4-dihydroxyphenylalanine (levodopa), which loses therapeutic efficacy and induces disabling abnormal involuntary movements known as levodopa-induced dyskinesia (LID) after several years. Evidence indicates that the pathophysiology of both PD and LID disorders is also associated with the dysfunctional activity of the serotonergic (5-HT) neurons that may be responsible for motor and non-motor disturbances. The main population of 5-HT neurons is located in the dorsal raphe nuclei (DRN), which provides extensive innervation to almost the entire neuroaxis and controls multiple functions in the brain. The degeneration of DRN 5-HT neurons occurs in early PD. These neurons can also take exogenous levodopa to transform it into dopamine, which may disturb neuron activity. This review will provide an overview of the underlying mechanisms responsible for 5-HT dysfunction and its clinical relevance in PD and dyskinesia.
帕金森病(PD)的特征是黑质多巴胺能神经元变性、纹状体多巴胺耗竭和含有α-突触核蛋白的路易小体的存在。临床上,存在涉及主要运动症状、运动徐缓、静止性震颤、肌肉僵硬和姿势异常的运动障碍,以及非运动症状,如睡眠、行为和情绪障碍。目前,PD 的治疗方法主要集中在通过 l-3,4-二羟基苯丙氨酸(左旋多巴)恢复多巴胺能神经传递,然而,经过数年,左旋多巴会失去治疗效果,并引起致残的异常不自主运动,即左旋多巴诱导的运动障碍(LID)。有证据表明,PD 和 LID 障碍的病理生理学也与 5-羟色胺(5-HT)神经元的功能障碍活动有关,这可能是导致运动和非运动障碍的原因。5-HT 神经元的主要群体位于中缝背核(DRN),它对几乎整个神经轴提供广泛的神经支配,并控制大脑中的多种功能。DRN 5-HT 神经元在早期 PD 中就会发生变性。这些神经元还可以摄取外源性的左旋多巴并将其转化为多巴胺,这可能会干扰神经元活动。本综述将概述导致 5-HT 功能障碍的潜在机制及其在 PD 和运动障碍中的临床相关性。