帕金森病的基因作用和治疗

Falaq Naz, Y. Siddique
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引用次数: 2

摘要

帕金森病(PD)是一种复杂的神经退行性疾病,主要是由于中脑黑质多巴胺能神经元的丧失而引起的。众所周知,多巴胺在黑质中合成,并通过黑质纹状体束转运到纹状体。除了散发形式的帕金森病外,也有家族性帕金森病病例,许多基因(常染色体显性和隐性)都与帕金森病有关。帕金森病没有永久性的治疗方法,迄今为止,左旋多巴治疗被认为是除了多巴胺激动剂之外的最佳选择。在目前的综述中,我们描述了PD的基因,多巴胺的作用,以及用于控制人类PD进展的治疗策略。
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Role of Genes and Treatments for Parkinson’s Disease
Parkinson’s Disease (PD) is a complex neurodegenerative disorder that mainly results due to the loss of dopaminergic neurons in the substantia nigra of the midbrain. It is well known that dopamine is synthesized in substantia nigra and is transported to the striatum via nigrostriatal tract. Besides the sporadic forms of PD, there are also familial cases of PD and number of genes (both autosomal dominant as well as recessive) are responsible for PD. There is no permanent cure for PD and to date, L-dopa therapy is considered to be the best option besides having dopamine agonists. In the present review, we have described the genes responsible for PD, the role of dopamine, and treatment strategies adopted for controlling the progression of PD in humans.
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