Gut microbiota reconstitution and control of α-synucleinopathy with β-glucans: a promising approach for individuals with parkinson's disease.

IF 3.5 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Faezeh Hatami, Zahra Aghelan, Mahan Rezaie Pouya, Melina Moulaeian, Ali Rastegari, Seyed Hosien Abtahi, Shaghayegh Hoseini
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引用次数: 0

Abstract

Parkinson's disease (PD) ranks as the second most prevalent neurodegenerative condition affecting individuals in their middle age and beyond. Its hallmark features include the abnormal accumulation of α-synuclein protein and the progressive loss of dopaminergic neurons. A substantial body of evidence supports the notion that an imbalance in the gut microbiome, known as dysbiosis, contributes to the misfolding and accumulation of α-synuclein, a key pathological feature of PD. This finding raises the possibility that restoring the gut microbiome, particularly the bacteria associated with α-synuclein, could serve as a promising therapeutic approach for PD. There is evidence that β-glucan can play an important role in the reconstitution of gut microbiome. In this regard, this study reviews the evidence showing the role of β-glucan in reducing α-synuclein accumulation and mitigating the progression of PD. This scooping review study presents promising prospects for advancing novel therapeutic approaches to benefit individuals with PD.

肠道菌群重建和β-葡聚糖控制α-突触核蛋白病:帕金森病患者的一种有希望的方法
帕金森病(PD)是影响中年及以上人群的第二大常见神经退行性疾病。其显著特征是α-突触核蛋白的异常积累和多巴胺能神经元的进行性丧失。大量证据支持这样一种观点,即肠道微生物群的失衡,即生态失调,导致α-突触核蛋白的错误折叠和积累,这是PD的一个关键病理特征。这一发现提出了一种可能性,即恢复肠道微生物群,特别是与α-突触核蛋白相关的细菌,可能是一种有希望的PD治疗方法。有证据表明β-葡聚糖在肠道菌群的重建中起重要作用。因此,本研究综述了β-葡聚糖在减少α-突触核蛋白积累和减缓PD进展中的作用。这项回顾性研究为推进PD患者的新型治疗方法提供了有希望的前景。
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来源期刊
Metabolic brain disease
Metabolic brain disease 医学-内分泌学与代谢
CiteScore
5.90
自引率
5.60%
发文量
248
审稿时长
6-12 weeks
期刊介绍: Metabolic Brain Disease serves as a forum for the publication of outstanding basic and clinical papers on all metabolic brain disease, including both human and animal studies. The journal publishes papers on the fundamental pathogenesis of these disorders and on related experimental and clinical techniques and methodologies. Metabolic Brain Disease is directed to physicians, neuroscientists, internists, psychiatrists, neurologists, pathologists, and others involved in the research and treatment of a broad range of metabolic brain disorders.
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