帕金森病、糖尿病和认知障碍。

Mohammad R Ashraghi, Gennaro Pagano, Sotirios Polychronis, Flavia Niccolini, Marios Politis
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引用次数: 0

摘要

背景:帕金森病是一种慢性神经退行性疾病,其特征是多巴胺能神经元的进行性丧失。帕金森病的病理生理机制尚不清楚。线粒体功能障碍、蛋白质异常聚集、神经炎症增加和脑糖代谢障碍是胰岛素抵抗、糖尿病和神经变性的共同过程,并被认为是帕金森病和认知障碍发展的关键机制。目的:综述帕金森病与糖尿病和认知功能障碍共同的病理生理基础的实验和临床证据。抗糖尿病药物和最近的胰岛素抵抗专利也可能被重新定位在帕金森病的治疗中。方法:采用MEDLINE数据库进行综述。结果:常见的抗糖尿病治疗方法,如DPP4抑制剂、GLP-1激动剂和二甲双胍,在治疗帕金森病和动物和人类认知障碍方面显示出希望。糖尿病和帕金森氏病之间常见的神经退行性变的病理生理学研究为新的治疗提供了可能。过去5年发布的专利可用于针对特定病理生理蛋白(如Nurr1、PINK1和NrF2)的帕金森病治疗新方法,而改善血脑屏障穿透的专利可提高现有治疗方法的疗效。结论:使用GLP-1激动剂和DPP-4抑制剂治疗PD的进一步研究是有必要的,因为它们显示出了希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Parkinson's Disease, Diabetes and Cognitive Impairment.

Background: Parkinson's disease is a chronic neurodegenerative disorder characterized by a progressive loss of dopaminergic neurons. The pathophysiological mechanisms underlying Parkinson's are still unknown. Mitochondrial dysfunction, abnormal protein aggregation, increased neuroinflammation and impairment of brain glucose metabolism are shared processes among insulinresistance, diabetes and neurodegeneration and have been suggested as key mechanisms in development of Parkinson's and cognitive impairment.

Objective: To review experimental and clinical evidence of underlying Parkinson's pathophysiology in common with diabetes and cognitive impairment. Anti-diabetic agents and recent patents for insulin-resistance that might be repositioned in the treatment of Parkinson's also have been included in this review.

Method: A narrative review using MEDLINE database.

Results: Common antidiabetic treatments such as DPP4 inhibitors, GLP-1 agonists and metformin have shown promise in the treatment of Parkinson's disease and cognitive impairment in animals and humans. Study of the pathophysiology of neurodegeneration common between diabetes and Parkinson's disease has given rise to new treatment possibilities. Patents published in the last 5 years could be used in novel approaches to Parkinson's treatment by targeting specific pathophysiology proteins, such as Nurr1, PINK1 and NrF2, while patents to improve penetration of the blood brain barrier could allow improved efficacy of existing treatments.

Conclusion: Further studies using GLP-1 agonists and DPP-4 inhibitors to treat PD are warranted as they have shown promise.

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