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二甲双胍作为前驱期帕金森病潜在神经保护剂的观点

Metformin as a Potential Neuroprotective Agent in Prodromal Parkinson's Disease-Viewpoint.

作者信息

Sportelli Carolina, Urso Daniele, Jenner Peter, Chaudhuri K Ray

机构信息

National Parkinson Foundation International Centre of Excellence, King's College Hospital, London, United Kingdom.

Institute of Psychiatry, Psychology & Neuroscience, King's College, London, United Kingdom.

出版信息

Front Neurol. 2020 Jun 12;11:556. doi: 10.3389/fneur.2020.00556. eCollection 2020.

Abstract

To date, there are no clinically effective neuroprotective or disease-modifying treatments that can halt Parkinson's disease (PD) progression. The current clinical approach focuses on symptomatic management. This failure may relate to the complex neurobiology underpinning the development of PD and the absence of true translational animal models. In addition, clinical diagnosis of PD relies on presentation of motor symptoms which occur when the neuropathology is already established. These multiple factors could contribute to the unsuccessful development of neuroprotective treatments for PD. Prodromal symptoms develop years prior to formal diagnosis and may provide an excellent tool for early diagnosis and better trial design. Patients with idiopathic rapid eye movement behavior disorder (iRBD) have the highest risk of developing PD and could represent an excellent group to include in neuroprotective trials for PD. In addition, repurposing drugs with excellent safety profiles is an appealing strategy to accelerate drug discovery. The anti-diabetic drug metformin has been shown to target diverse cellular pathways implicated in PD progression. Multiple studies have, additionally, observed the benefits of metformin to counteract other age-related diseases. The purpose of this viewpoint is to discuss metformin's neuroprotective potential by outlining relevant mechanisms of action and the selection of iRBD patients for future clinical trials in PD.

摘要

迄今为止,尚无临床有效的神经保护或疾病修饰疗法能够阻止帕金森病(PD)的进展。目前的临床方法侧重于对症治疗。这种失败可能与PD发生发展背后复杂的神经生物学以及缺乏真正可转化的动物模型有关。此外,PD的临床诊断依赖于运动症状的出现,而这些症状在神经病理学已经确立时才会出现。这些多种因素可能导致PD神经保护治疗的研发失败。前驱症状在正式诊断前数年就已出现,可能为早期诊断和更好的试验设计提供绝佳工具。特发性快速眼动睡眠行为障碍(iRBD)患者患PD的风险最高,可能是纳入PD神经保护试验的理想人群。此外,重新利用具有良好安全性的药物是加速药物研发的一种有吸引力的策略。抗糖尿病药物二甲双胍已被证明可作用于与PD进展相关的多种细胞途径。另外,多项研究观察到二甲双胍对对抗其他与年龄相关疾病的益处。本文观点的目的是通过概述相关作用机制以及选择iRBD患者用于未来PD临床试验,来探讨二甲双胍的神经保护潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2d/7304367/47ac7324880a/fneur-11-00556-g0001.jpg

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