Mary Dayne Sia Tai, Gloria Gamiz-Arco, Aurora Martinez
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引用次数: 0
Abstract
Parkinsonism is the primary type of movement disorder in adults, encompassing a set of clinical symptoms, including rigidity, tremors, dystonia, bradykinesia, and postural instability. These symptoms are primarily caused by a deficiency in dopamine (DA), an essential neurotransmitter in the brain. Currently, the DA precursor levodopa (synthetic L-DOPA) is the standard medication to treat DA deficiency, but it only addresses symptoms rather than provides a cure. In this review, we provide an overview of disorders associated with DA dysregulation and deficiency, particularly Parkinson's disease and rare inherited disorders leading predominantly to dystonia and/or parkinsonism, even in childhood. Although levodopa is relatively effective for the management of motor dysfunctions, it is less effective for severe forms of parkinsonism and is also associated with side effects and a loss of efficacy over time. We present ongoing efforts to reinforce the effect of levodopa and to develop innovative therapies that target the underlying pathogenic mechanisms affecting DA synthesis and transport, increasing neurotransmission through disease-modifying approaches, such as cell-based therapies, nucleic acid- and protein-based biologics, and small molecules.
帕金森病是成人运动障碍的主要类型,包括一系列临床症状,包括僵直、震颤、肌张力障碍、运动迟缓和姿势不稳。这些症状主要是由于缺乏多巴胺(DA)引起的,多巴胺是大脑中一种重要的神经递质。目前,DA 前体左旋多巴(合成 L-DOPA)是治疗 DA 缺乏症的标准药物,但它只能缓解症状,而不能治愈疾病。在这篇综述中,我们将概述与DA调节失调和缺乏有关的疾病,尤其是帕金森病和罕见的遗传性疾病,这些疾病主要导致肌张力障碍和/或帕金森病,甚至在儿童时期就已出现。虽然左旋多巴对运动功能障碍的治疗相对有效,但对严重帕金森病的治疗效果较差,而且随着时间的推移,还伴有副作用和疗效减退。我们正在努力加强左旋多巴的疗效,并开发针对影响 DA 合成和转运的潜在致病机制的创新疗法,通过基于细胞的疗法、基于核酸和蛋白质的生物制剂以及小分子药物等疾病调节方法增加神经传递。
期刊介绍:
Biochemical Society Transactions is the reviews journal of the Biochemical Society. Publishing concise reviews written by experts in the field, providing a timely snapshot of the latest developments across all areas of the molecular and cellular biosciences.
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