Li Jingwen, Liu Tingting, Xian Meiyan, Wei Jianshe
Institute for Sports and Brain Health, School of Physical Education, Henan University, Kaifeng, 475004, Henan, China.
Institute for Brain Sciences Research, School of Life Sciences, Henan University, Kaifeng, 475004, China.
Mol Cell Biochem. 2025 May 13. doi: 10.1007/s11010-025-05299-8.
Neurodegenerative diseases comprise a group of central nervous system disorders marked by progressive neuronal degeneration and dysfunction. Their pathogenesis is multifactorial, involving oxidative stress, mitochondrial dysfunction, excitotoxicity, and neuroinflammation. Recent research has highlighted the potential of exercise as a non-pharmacological intervention for both the prevention and treatment of these disorders. In particular, exercise has received growing attention for its capacity to upregulate the expression and activity of SIRT1, a critical mediator of neuroprotection via downstream signaling pathways. SIRT1, a key member of the Sirtuin family, is a nicotinamide adenine dinucleotide (NAD +)-dependent class III histone deacetylase. It plays an essential role in regulating cellular metabolism, energy homeostasis, gene expression, and cellular longevity. In the context of neurodegenerative diseases, SIRT1 confers neuroprotection by modulating multiple signaling cascades through deacetylation, suppressing neuronal apoptosis, and promoting neural repair and regeneration. Exercise enhances SIRT1 expression and activity by increasing NAD + synthesis and utilization, improving intracellular redox balance, alleviating oxidative stress-induced inhibition of SIRT1, and thereby promoting its activation. Moreover, exercise may indirectly modulate SIRT1 function by influencing interacting molecular networks. This review summarizes recent advances in the therapeutic application of exercise for neurodegenerative diseases, with a focus on SIRT1 as a central mechanism. It examines how exercise mediates neuroprotection through the regulation of SIRT1 and its associated molecular mechanisms and signaling pathways. Finally, the paper discusses the potential applications and challenges of integrating exercise and SIRT1-targeted strategies in the management of neurodegenerative diseases, offering novel perspectives for the development of innovative treatments and improvements in patients' quality of life.
神经退行性疾病是一组以进行性神经元变性和功能障碍为特征的中枢神经系统疾病。其发病机制是多因素的,涉及氧化应激、线粒体功能障碍、兴奋性毒性和神经炎症。最近的研究强调了运动作为预防和治疗这些疾病的非药物干预措施的潜力。特别是,运动因其上调SIRT1表达和活性的能力而受到越来越多的关注,SIRT1是通过下游信号通路发挥神经保护作用的关键介质。SIRT1是沉默调节蛋白家族的关键成员,是一种烟酰胺腺嘌呤二核苷酸(NAD+)依赖性III类组蛋白脱乙酰酶。它在调节细胞代谢、能量稳态、基因表达和细胞寿命方面发挥着重要作用。在神经退行性疾病的背景下,SIRT1通过去乙酰化调节多个信号级联反应、抑制神经元凋亡以及促进神经修复和再生来赋予神经保护作用。运动通过增加NAD+的合成和利用、改善细胞内氧化还原平衡、减轻氧化应激对SIRT1的抑制作用,从而促进其激活,进而增强SIRT1的表达和活性。此外,运动可能通过影响相互作用的分子网络间接调节SIRT1的功能。本综述总结了运动在神经退行性疾病治疗应用方面的最新进展,重点关注SIRT1这一核心机制。它研究了运动如何通过调节SIRT1及其相关分子机制和信号通路来介导神经保护作用。最后,本文讨论了将运动和以SIRT1为靶点的策略整合到神经退行性疾病管理中的潜在应用和挑战,为开发创新治疗方法和改善患者生活质量提供了新的视角。
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