Combating Dopaminergic Neurodegeneration in Parkinson’s Disease through Nanovesicle Technology

神经退行性变 帕金森病 多巴胺能 医学 神经炎症 多巴胺 神经科学 疾病 药品 药理学 神经保护 自噬 生物 内科学 细胞凋亡 生物化学
作者
Rubina Roy,Rajib Paul,Pallab Bhattacharya,Anupom Borah
出处
期刊:ACS Chemical Neuroscience [American Chemical Society]
卷期号:14 (16): 2830-2848 被引量:3
标识
DOI:10.1021/acschemneuro.3c00070
摘要

Parkinson's disease (PD) is characterized by dopaminergic neurodegeneration, resulting in dopamine depletion and motor behavior deficits. Since the discovery of L-DOPA, it has been the most prescribed drug for symptomatic relief in PD, whose prolonged use, however, causes undesirable motor fluctuations like dyskinesia and dystonia. Further, therapeutics targeting the pathological hallmarks of PD including α-synuclein aggregation, oxidative stress, neuroinflammation, and autophagy impairment have also been developed, yet PD treatment is a largely unmet success. The inception of the nanovesicle-based drug delivery approach over the past few decades brings add-on advantages to the therapeutic strategies for PD treatment in which nanovesicles (basically phospholipid-containing artificial structures) are used to load and deliver drugs to the target site of the body. The present review narrates the characteristic features of nanovesicles including their blood–brain barrier permeability and ability to reach dopaminergic neurons of the brain and finally discusses the current status of this technology in the treatment of PD. From the review, it becomes evident that with the assistance of nanovesicle technology, the therapeutic efficacy of anti-PD pharmaceuticals, phyto-compounds, as well as that of nucleic acids targeting α-synuclein aggregation gained a significant increment. Furthermore, owing to the multiple drug-carrying abilities of nanovesicles, combination therapy targeting multiple pathogenic events of PD has also found success in preclinical studies and will plausibly lead to effective treatment strategies in the near future.
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