丝氨酸
活性氧
细胞生物学
磷酸化
氧化磷酸化
生物化学
生物
调节器
化学
基因
作者
Feng Zheng,Shuai Liu,Wei Tian,Lei Wang,Yuanyuan Chang,Hao Qu,Lei Zheng
出处
期刊:PubMed
日期:2025-07-18
卷期号:11 (29): eadr8592-eadr8592
被引量:1
标识
DOI:10.1126/sciadv.adr8592
摘要
Prolonged sleep deprivation (SD) results in increased accumulation of reactive oxygen species (ROS) in gut, although the underlying mechanisms remain to be elucidated. This study identifies d-serine as a crucial regulator of gut ROS during SD. Knockdown of serine racemase (SR), the enzyme responsible for d-serine production, prevents the enhanced ROS buildup during SD in Drosophila. Gut enterocytes (ECs) respond to γ-aminobutyric acid (GABA) signaling by producing d-serine, which influences downstream N-methyl-d-aspartate receptor (NMDAR) activity and modulates sleep pressure. However, the continuous demand for sleep disrupts this feedback loop. Prolonged SD leads to increased levels of d-serine in the gut, an elevated pyruvate pool in ECs, enhanced mitochondrial oxidative phosphorylation, impaired lipid metabolism in peroxisomes, and the accumulation of harmful ROS. In conclusion, our findings illuminate the metabolic alterations and brain-gut communication pathways that may contribute to the increase in gut d-serine and subsequent ROS accumulation induced by SD.
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