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从大脑到肌肉:肌肉组织在神经退行性疾病中的作用

From Brain to Muscle: The Role of Muscle Tissue in Neurodegenerative Disorders.

作者信息

Duranti Elisa, Villa Chiara

机构信息

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

出版信息

Biology (Basel). 2024 Sep 12;13(9):719. doi: 10.3390/biology13090719.

Abstract

Neurodegenerative diseases (NDs), like amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD), and Parkinson's disease (PD), primarily affect the central nervous system, leading to progressive neuronal loss and motor and cognitive dysfunction. However, recent studies have revealed that muscle tissue also plays a significant role in these diseases. ALS is characterized by severe muscle wasting as a result of motor neuron degeneration, as well as alterations in gene expression, protein aggregation, and oxidative stress. Muscle atrophy and mitochondrial dysfunction are also observed in AD, which may exacerbate cognitive decline due to systemic metabolic dysregulation. PD patients exhibit muscle fiber atrophy, altered muscle composition, and α-synuclein aggregation within muscle cells, contributing to motor symptoms and disease progression. Systemic inflammation and impaired protein degradation pathways are common among these disorders, highlighting muscle tissue as a key player in disease progression. Understanding these muscle-related changes offers potential therapeutic avenues, such as targeting mitochondrial function, reducing inflammation, and promoting muscle regeneration with exercise and pharmacological interventions. This review emphasizes the importance of considering an integrative approach to neurodegenerative disease research, considering both central and peripheral pathological mechanisms, in order to develop more effective treatments and improve patient outcomes.

摘要

神经退行性疾病(NDs),如肌萎缩侧索硬化症(ALS)、阿尔茨海默病(AD)和帕金森病(PD),主要影响中枢神经系统,导致神经元进行性丧失以及运动和认知功能障碍。然而,最近的研究表明,肌肉组织在这些疾病中也起着重要作用。ALS的特征是由于运动神经元变性导致严重的肌肉萎缩,以及基因表达、蛋白质聚集和氧化应激的改变。AD中也观察到肌肉萎缩和线粒体功能障碍,这可能由于全身代谢失调而加剧认知衰退。PD患者表现出肌纤维萎缩、肌肉组成改变以及肌肉细胞内α-突触核蛋白聚集,这导致运动症状和疾病进展。全身炎症和蛋白质降解途径受损在这些疾病中很常见,突出了肌肉组织在疾病进展中的关键作用。了解这些与肌肉相关的变化提供了潜在的治疗途径,如靶向线粒体功能、减轻炎症以及通过运动和药物干预促进肌肉再生。这篇综述强调了采用综合方法进行神经退行性疾病研究的重要性,既要考虑中枢病理机制,也要考虑外周病理机制,以便开发更有效的治疗方法并改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a62/11428675/0610dd091882/biology-13-00719-g001.jpg

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