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运动驱动的细胞自噬:通往全身健康的桥梁。

Exercise-driven cellular autophagy: A bridge to systematic wellness.

作者信息

Zhou Xiao-Han, Luo Ya-Xi, Yao Xiu-Qing

机构信息

Department of Rehabilitation, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, PR China.

Department of Rehabilitation, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, PR China; Chongqing Municipality Clinical Research Center for Geriatric Medicine, Chongqing, PR China; Department of Rehabilitation Therapy, Chongqing Medical University, Chongqing, PR China.

出版信息

J Adv Res. 2025 Jan 3. doi: 10.1016/j.jare.2024.12.036.

Abstract

BACKGROUND

Exercise enhances health by supporting homeostasis, bolstering defenses, and aiding disease recovery. It activates autophagy, a conserved cellular process essential for maintaining balance, while dysregulated autophagy contributes to disease progression. Despite extensive research on exercise and autophagy independently, their interplay remains insufficiently understood.

AIM OF REVIEW

This review explores the molecular mechanisms of exercise-induced autophagy in various tissues, focusing on key transduction pathways. It examines how different types of exercise trigger specific autophagic responses, supporting cellular balance and addressing systemic dysfunctions. The review also highlights the signaling pathways involved, their roles in protecting organ function, reducing disease risk, and promoting longevity, offering a clear understanding of the link between exercise and autophagy.

KEY SCIENTIFIC CONCEPTS OF REVIEW

Exercise-induced autophagy is governed by highly coordinated and dynamic pathways integrating direct and indirect mechanical forces and biochemical signals, linking physical activity to cellular and systemic health across multiple organ systems. Its activation is influenced by exercise modality, intensity, duration, and individual biological characteristics, including age, sex, and muscle fiber composition. Aerobic exercises primarily engage AMPK and mTOR pathways, supporting mitochondrial quality and cellular homeostasis. Anaerobic training activates PI3K/Akt signaling, modulating molecules like FOXO3a and Beclin1 to drive muscle autophagy and repair. In pathological contexts, exercise-induced autophagy enhances mitochondrial function, proteostasis, and tissue regeneration, benefiting conditions like sarcopenia, neurodegeneration, myocardial ischemia, metabolic disorders, and cancer. However, excessive exercise may lead to autophagic overactivation, leading to muscle atrophy or pathological cardiac remodeling. This underscores the critical need for balanced exercise regimens to maximize therapeutic efficacy while minimizing risks. Future research should prioritize identifying reliable biomarkers, optimizing exercise protocols, and integrating exercise with pharmacological strategies to enhance therapeutic outcomes.

摘要

背景

运动通过维持体内平衡、增强防御能力和促进疾病恢复来增进健康。运动激活自噬,这是一种对维持平衡至关重要的保守细胞过程,而自噬失调则会促进疾病进展。尽管对运动和自噬已分别进行了广泛研究,但它们之间的相互作用仍未得到充分理解。

综述目的

本综述探讨运动诱导的自噬在各种组织中的分子机制,重点关注关键转导途径。研究不同类型的运动如何引发特定的自噬反应,维持细胞平衡并解决全身功能障碍。该综述还强调了相关的信号通路、它们在保护器官功能、降低疾病风险和促进长寿方面的作用,从而清晰地阐明运动与自噬之间的联系。

综述的关键科学概念

运动诱导的自噬受高度协调且动态的途径调控,这些途径整合了直接和间接的机械力以及生化信号,将身体活动与多个器官系统的细胞和全身健康联系起来。其激活受运动方式、强度、持续时间以及个体生物学特征(包括年龄、性别和肌纤维组成)的影响。有氧运动主要涉及AMPK和mTOR途径,有助于维持线粒体质量和细胞内稳态。无氧训练激活PI3K/Akt信号通路,调节FOXO3a和Beclin1等分子,以驱动肌肉自噬和修复。在病理情况下,运动诱导的自噬可增强线粒体功能、蛋白质稳态和组织再生,对肌肉减少症、神经退行性变、心肌缺血、代谢紊乱和癌症等病症有益。然而,过度运动可能导致自噬过度激活,进而导致肌肉萎缩或病理性心脏重塑。这凸显了制定平衡运动方案的迫切需求,以在将风险降至最低的同时最大化治疗效果。未来的研究应优先确定可靠的生物标志物、优化运动方案,并将运动与药物策略相结合以提高治疗效果。

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