神经保护
神经科学
生物
功能基因组学
粒体自噬
神经退行性变
线粒体
代谢组学
氧化应激
细胞应激反应
计算生物学
细胞代谢
离体
自噬
休眠(计算)
糖酵解
神经可塑性
体内
程序性细胞死亡
模式生物
脑缺血
生物信息学
细胞生物学
作者
Lavanya Gupta,Sriya Amati,K. Dengke,Neel S. Singhal
标识
DOI:10.1016/j.expneurol.2025.115558
摘要
Hibernating animals are a remarkable model for natural neuroprotection, demonstrating profound ischemia tolerance in diverse in vivo and ex vivo models. Recent advances in functional genomics, transcriptomics, proteomics, and metabolomics have enabled detailed dissection of these resilience pathways in brain tissue and cell models derived from hibernating species, such as the Arctic ground squirrel. Major adaptations include shifts from glycolytic to lipid-based and oxidative metabolism, upregulation of antioxidant networks, dynamic regulation of mitochondrial structure and function, and extensive cytoskeletal remodeling to support plasticity. Studies using -omics technologies further highlight critical roles for molecular chaperones, post-transcriptional control, and non-coding regulatory DNA in orchestrating hibernation phenotypes. Functional screens and pre-clinical studies link these pathways to enhanced neuronal survival under metabolic stress in vivo. Lessons from naturally resilient species hold promise for developing more effective neuroprotective and neurorecovery therapies in human stroke and brain injury. Future translational success will require precise, multi-pathway therapeutic strategies that recapitulate the coordinated resilience programs observed in hibernators.
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