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色氨酸和苯丙氨酸产生的肠道细菌代谢产物可诱导小鼠褪黑素合成并延长睡眠时间。

Gut Bacterial Metabolites from Tryptophan and Phenylalanine Induce Melatonin Synthesis and Extend Sleep Duration in Mice.

作者信息

Lee Ji-Hyeok, Hwang Su Jung, Ham Song Lim, Kim Jonghwan, Bang Hye Jung, Park Joon-Suk, Jang Hyun-Hee, Kim Tae Yang, Park Jeong Woo, Seo Young Rok, Kim Byeong Soo, Kim Gon Sup, Lee Hyo-Jong, Kim Chung Sub

机构信息

Department of Biohealth Regulatory Science, Sungkyunkwan University, Suwon 16419, Republic of Korea.

School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.

出版信息

ACS Omega. 2024 Oct 15;9(43):43875-43883. doi: 10.1021/acsomega.4c06923. eCollection 2024 Oct 29.

Abstract

The human gut microbiota significantly influences various physiological systems, including immune, nervous, and metabolic systems. Recent studies suggest that gut microbiota may affect sleep quality with certain bacteria and metabolites being linked to sleep patterns. However, the underlying chemical signaling pathway remains unclear. In this study, we investigated the effect of four gut bacteria-derived metabolites, tryptamine (), indolokine A5 (), 2-(1'-indole-3'-carbonyl)-thiazole-4-carboxylic acid methyl ester (ITE, ), and phenethylamine (PEA, ), on sleep characteristics in mice and melatonin biosynthesis pathways in zebrafish. Their sleep-promoting effects were evaluated in a pentobarbital-induced sleep mouse model, revealing significant increases in sleep duration and blood melatonin levels, particularly with ITE () and PEA (). Further tests in zebrafish embryos showed that ITE () and PEA () increased the expression of genes for melatonin biosynthesis (, , , and ) in a concentration-dependent manner, indicating their potential as therapeutic agents for sleep disorders.

摘要

人类肠道微生物群对包括免疫、神经和代谢系统在内的各种生理系统有显著影响。最近的研究表明,肠道微生物群可能会影响睡眠质量,某些细菌和代谢产物与睡眠模式有关。然而,潜在的化学信号通路仍不清楚。在本研究中,我们研究了四种肠道细菌衍生的代谢产物,色胺()、吲哚洛金A5()、2-(1'-吲哚-3'-羰基)-噻唑-4-羧酸甲酯(ITE,)和苯乙胺(PEA,)对小鼠睡眠特征和斑马鱼褪黑素生物合成途径的影响。在戊巴比妥诱导的睡眠小鼠模型中评估了它们的促睡眠作用,结果显示睡眠时间和血液褪黑素水平显著增加,尤其是ITE()和PEA()。在斑马鱼胚胎中的进一步测试表明,ITE()和PEA()以浓度依赖的方式增加了褪黑素生物合成相关基因(、、、和)的表达,表明它们作为睡眠障碍治疗药物的潜力。

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