肠道菌群和代谢物的改变有助于术后睡眠障碍。

Q1 Health Professions
Hui Zhong, Meiru Jiang, Kun Yuan, Fang Sheng, Xiuyun Xu, Yong Cui, Xijia Sun, Wenfei Tan
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引用次数: 0

摘要

背景:肠道菌群的组成及其代谢产物影响术后患者的睡眠。方法:我们旨在阐明肠道菌群紊乱调节宿主术后睡眠障碍的病理生理机制。在这项研究中,我们探讨了麻醉、手术和术后睡眠时间对术后被分类为睡眠不良(PS)和睡眠良好(GS)的个体粪便微生物群和代谢物的影响,并通过双谱指数进行了诊断。我们还对伪无菌(PGF)大鼠进行了粪便微生物群移植,并应用Western blotting、免疫组织化学和肠通透性分析来确定其作用的潜在机制。结果:研究发现,PS组术后粪便代谢产物色氨酸和犬尿氨酸水平明显高于GS组。PGF组大鼠的快速眼动睡眠(REM)低于GS组大鼠(GS-PGF: 11.4%±1.6%,PS-PGF: 4.8%±2.0%,p)结论:术后肠道生态失调和5-羟色胺代谢缺陷可能导致术后睡眠障碍。临床医生和睡眠研究人员可能会从这项研究中获得新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alterations in gut microbiota and metabolites contribute to postoperative sleep disturbances

Alterations in gut microbiota and metabolites contribute to postoperative sleep disturbances

Background

The composition of the intestinal flora and the resulting metabolites affect patients' sleep after surgery.

Methods

We intended to elucidate the mechanisms by which disordered intestinal flora modulate the pathophysiology of postoperative sleep disturbances in hosts. In this study, we explored the impacts of anesthesia, surgery, and postoperative sleep duration on the fecal microbiota and metabolites of individuals classified postprocedurally as poor sleepers (PS) and good sleepers (GS), as diagnosed by the bispectral index. We also performed fecal microbiota transplantation in pseudo-germ-free (PGF) rats and applied Western blotting, immunohistochemistry, and gut permeability analyses to identify the potential mechanism of its effect.

Results

Research finding shows the PS group had significantly higher postoperative stool levels of the metabolites tryptophan and kynurenine than the GS group. PGF rats that received gut microbiota from PSs exhibited less rapid eye movement (REM) sleep than those that received GS microbiota (GS-PGF: 11.4% ± 1.6%, PS-PGF: 4.8% ± 2.0%, p < 0.001). Measurement of 5-hydroxytryptophan (5-HTP) levels in the stool, serum, and prefrontal cortex (PFC) indicated that altered 5-HTP levels, including reduced levels in the PFC, caused sleep loss in PGF rats transplanted with PS gut flora. Through the brain–gut axis, the inactivity of tryptophan hydroxylase 1 (TPH1) and TPH2 in the colon and PFC, respectively, caused a loss of REM sleep in PGF rats and decreased the 5-HTP level in the PFC.

Conclusions

These findings indicate that postoperative gut dysbiosis and defective 5-HTP metabolism may cause postoperative sleep disturbances. Clinicians and sleep researchers may gain new insights from this study.

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CiteScore
5.50
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