Feeney Sierra P, McCarthy Jordan M, Petruconis Cecilia R, Tudor Jennifer C
Department of Biology, College of Arts and Sciences, Saint Joseph's University, Philadelphia, PA 19131, USA.
Sci Signal. 2025 Apr 8;18(881):eadp9358. doi: 10.1126/scisignal.adp9358.
Sleep loss dysregulates cellular metabolism and energy homeostasis. Highly metabolically active cells, such as neurons, enter a catabolic state during periods of sleep loss, which consequently disrupts physiological functioning. Specific to the central nervous system, sleep loss results in impaired synaptogenesis and long-term memory, effects that are also characteristic of neurodegenerative diseases. In this review, we describe how sleep deprivation increases resting energy expenditure, leading to the development of a negative energy balance-a state with insufficient metabolic resources to support energy expenditure-in highly active cells like neurons. This disruption of energetic homeostasis alters the balance of metabolites, including adenosine, lactate, and lipid peroxides, such that energetically costly processes, such as synapse formation, are attenuated. During sleep loss, metabolically active cells shunt energetic resources away from those processes that are not acutely essential, like memory formation, to support cell survival. Ultimately, these findings characterize sleep loss as a metabolic disorder.
睡眠不足会破坏细胞代谢和能量平衡。高度活跃的代谢细胞,如神经元,在睡眠不足期间会进入分解代谢状态,从而扰乱生理功能。在中枢神经系统中,睡眠不足会导致突触形成受损和长期记忆受损,这些影响也是神经退行性疾病的特征。在这篇综述中,我们描述了睡眠剥夺如何增加静息能量消耗,导致负能量平衡的发展——一种代谢资源不足以支持能量消耗的状态——在像神经元这样的高活性细胞中。这种能量平衡的破坏改变了包括腺苷、乳酸和脂质过氧化物在内的代谢物平衡,使得诸如突触形成等能量消耗大的过程减弱。在睡眠不足期间,代谢活跃的细胞将能量资源从那些并非急需的过程(如记忆形成)转移开,以支持细胞存活。最终,这些发现将睡眠不足表征为一种代谢紊乱。