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帕金森病治疗中的新老挑战

Old and new challenges in Parkinson's disease therapeutics.

作者信息

Pires Ana O, Teixeira F G, Mendes-Pinheiro B, Serra Sofia C, Sousa Nuno, Salgado António J

机构信息

Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.

Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.

出版信息

Prog Neurobiol. 2017 Sep;156:69-89. doi: 10.1016/j.pneurobio.2017.04.006. Epub 2017 Apr 27.

Abstract

Parkinson's disease (PD) is a neurodegenerative disorder characterized by the degeneration of dopaminergic neurons and/or loss od neuronal projections, in several dopaminergic networks. Current treatments for idiopathic PD rely mainly on the use of pharmacologic agents to improve motor symptomatology of PD patients. Nevertheless, so far PD remains an incurable disease. Therefore, it is of utmost importance to establish new therapeutic strategies for PD treatment. Over the last 20 years, several molecular, gene and cell/stem-cell therapeutic approaches have been developed with the aim of counteracting or retarding PD progression. The scope of this review is to provide an overview of PD related therapies and major breakthroughs achieved within this field. In order to do so, this review will start by focusing on PD characterization and current treatment options covering thereafter molecular, gene and cell/stem cell-based therapies that are currently being studied in animal models of PD or have recently been tested in clinical trials. Among stem cell-based therapies, those using MSCs as possible disease modifying agents for PD therapy and, specifically, the MSCs secretome contribution to meet the clinical challenge of counteracting or retarding PD progression, will be more deeply explored.

摘要

帕金森病(PD)是一种神经退行性疾病,其特征是多个多巴胺能网络中的多巴胺能神经元变性和/或神经元投射丧失。目前特发性帕金森病的治疗主要依赖使用药物来改善帕金森病患者的运动症状。然而,迄今为止帕金森病仍然是一种无法治愈的疾病。因此,建立新的帕金森病治疗策略至关重要。在过去20年里,已经开发了几种分子、基因和细胞/干细胞治疗方法,旨在对抗或延缓帕金森病的进展。本综述的范围是概述与帕金森病相关的治疗方法以及该领域取得的重大突破。为了做到这一点,本综述将首先关注帕金森病的特征和当前的治疗选择,随后涵盖目前正在帕金森病动物模型中研究或最近已在临床试验中测试的基于分子、基因和细胞/干细胞的治疗方法。在基于干细胞的治疗方法中,将更深入地探讨那些使用间充质干细胞作为可能改善帕金森病病情的药物,特别是间充质干细胞分泌组在应对或延缓帕金森病进展的临床挑战方面的作用。

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