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虾青素在神经退行性疾病治疗中的生物学活性。

Biological activities of astaxanthin in the treatment of neurodegenerative diseases.

作者信息

Lotfi Alireza, Abroodi Zahra, Khazaei Mozafar

机构信息

Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Department of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Neurodegener Dis Manag. 2024;14(6):241-256. doi: 10.1080/17582024.2024.2433932. Epub 2024 Dec 8.

Abstract

INTRODUCTION

Neurodegenerative diseases (NDs) develop with the gradual advancement of neuronal damage and dysfunction in the central nervous system (CNS). These disorders are mostly the outcomes of the improper sedimentation and accumulation of proteins, such as amyloid-β (Aβ), α-synuclein, and prions. Astaxanthin (AST) exists in different types of living organisms and displays antioxidant and anti-inflammatory functions. This review has concentrated on the therapeutic characteristics of AST on NDs.

METHODS

Data was collected by searching Scopus, PubMed, and Google Scholar databases. Articles selected for this review reported results on the neuroprotective properties of AST on NDs of studies conducted during the years 2000 to 2024.

RESULTS

AST decreases soluble Aβ levels by stimulating the Aβ degradation enzyme. It also reduces inflammation in the substantia nigra (SN) by decreasing IBA1 expression, thereby lessening microglia activity. This carotenoid reduces demyelination by increasing the survival of oligodendrocytes cells and increasing the number of their progenitor cells. AST has antioxidant, anti-inflammatory, and anti-apoptotic properties and can play a role in the treatment of many NDs.

CONCLUSION

There is no definitive treatment for some NDs. The use of AST and natural compounds can be an optimal method for preventing and treating NDs with few side effects.

摘要

引言

神经退行性疾病(NDs)随着中枢神经系统(CNS)中神经元损伤和功能障碍的逐渐发展而出现。这些疾病大多是蛋白质(如β淀粉样蛋白(Aβ)、α-突触核蛋白和朊病毒)异常沉积和积累的结果。虾青素(AST)存在于不同类型的生物体中,具有抗氧化和抗炎功能。本综述集中探讨了AST对神经退行性疾病的治疗特性。

方法

通过检索Scopus、PubMed和谷歌学术数据库收集数据。本综述所选文章报告了2000年至2024年期间进行的关于AST对神经退行性疾病神经保护特性研究的结果。

结果

AST通过刺激Aβ降解酶降低可溶性Aβ水平。它还通过降低IBA1表达减少黑质(SN)中的炎症,从而降低小胶质细胞活性。这种类胡萝卜素通过提高少突胶质细胞的存活率并增加其祖细胞数量来减少脱髓鞘。AST具有抗氧化、抗炎和抗凋亡特性,可在多种神经退行性疾病的治疗中发挥作用。

结论

某些神经退行性疾病尚无确切的治疗方法。使用AST和天然化合物可能是预防和治疗神经退行性疾病且副作用较少的最佳方法。

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