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细胞外囊泡、细胞穿透肽和微小RNA作为帕金森病和阿尔茨海默病未来的新型治疗干预手段

Extracellular Vesicles, Cell-Penetrating Peptides and miRNAs as Future Novel Therapeutic Interventions for Parkinson's and Alzheimer's Disease.

作者信息

Keighron Cameron Noah, Avazzadeh Sahar, Goljanek-Whysall Katarzyna, McDonagh Brian, Howard Linda, Ritter Thomas, Quinlan Leo R

机构信息

Physiology School of Medicine, University of Galway, H91 TK33 Galway, Ireland.

Cellular Physiology Research Laboratory (CPRL), School of Medicine, University of Galway, H91 TK33 Galway, Ireland.

出版信息

Biomedicines. 2023 Feb 28;11(3):728. doi: 10.3390/biomedicines11030728.

Abstract

Neurodegeneration is hallmarked by the progressive loss of dopaminergic neurons and/or a significant increase in protein aggregates in the brain. Neurodegenerative diseases are a leading cause of death worldwide with over 15 million people currently suffering from either Parkinson's disease (PD) or Alzheimer's disease (AD). PD is often characterized by both motor and non-motor symptoms, including muscle rigidity, tremors and bradykinesia, with AD displaying symptoms of confusion and dementia. The current mainstay of therapeutics includes pharmacological approaches such as levodopa to replace dopamine in PD patients, deep brain stimulation in affected regions of the brain and physical therapy. However, these treatments are typically not disease-modifying, though they do help at least for some time with symptom management. These treatments often also fail due to their inability to cross the blood-brain barrier. There is a need to develop new strategies to target neurodegeneration in an ever-ageing population. First, we review the current PD and AD treatments and their limitations. Second, we review the current use of extracellular vesicles (EVs), cell-penetrating peptides (CPPs) and miRNAs as neuroprotective agents. Finally, we discuss the possibility of exploiting these as a combinatory therapeutic, alongside some potential drawbacks.

摘要

神经退行性变的特征是大脑中多巴胺能神经元逐渐丧失和/或蛋白质聚集体显著增加。神经退行性疾病是全球主要的死亡原因之一,目前有超过1500万人患有帕金森病(PD)或阿尔茨海默病(AD)。PD通常表现为运动和非运动症状,包括肌肉僵硬、震颤和运动迟缓,而AD则表现为认知混乱和痴呆症状。目前的主要治疗方法包括药理学方法,如左旋多巴用于替代PD患者体内的多巴胺、对大脑受影响区域进行深部脑刺激以及物理治疗。然而,这些治疗通常并不能改变疾病进程,尽管它们至少在一段时间内有助于症状管理。这些治疗方法往往还会因为无法穿过血脑屏障而失效。在人口老龄化日益严重的情况下,需要开发针对神经退行性变的新策略。首先,我们回顾当前PD和AD的治疗方法及其局限性。其次,我们回顾细胞外囊泡(EVs)、细胞穿透肽(CPPs)和微小RNA(miRNAs)作为神经保护剂的当前应用情况。最后,我们讨论将这些作为联合治疗方法的可能性以及一些潜在的缺点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d947/10045119/36586b32b442/biomedicines-11-00728-g001.jpg

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