Department of Emergency, Xijing Hospital, Air Force Medical University, Xi'an, 710032, Shaanxi, China.
Mol Biotechnol. 2024 Aug;66(8):1961-1969. doi: 10.1007/s12033-023-00809-9. Epub 2023 Jul 29.
This study aims to reveal the metabolic differences between SDC-1 knockout mice and wild-type mice and the metabolic differences caused by shock in SDC-1 knockout mice by integrating transcriptomics and metabolomics. A total of 1009 differential metabolites were differentially expressed based on untargeted metabolomics and high-resolution mass spectrometry detection techniques. According to Kyoto Encyclopedia of Genes and Genomes enrichment, SDC-1 knockout significantly altered fat digestion and absorption, GnRH signaling pathway, fructose and mannose metabolism, and some other amino-related metabolic pathways and significantly modulated positively regulated longevity regulatory pathways, longevity regulatory pathways-worm, nicotinamide and niacinamide metabolism, and vitamin digestion and absorption pathways after its shock. Our findings indicate that SDC-1 knockout may have potential therapeutic effects in hemorrhagic shock by increasing nicotinamide metabolism.
本研究旨在通过整合转录组学和代谢组学,揭示 SDC-1 敲除小鼠与野生型小鼠之间的代谢差异,以及 SDC-1 敲除小鼠休克引起的代谢差异。基于非靶向代谢组学和高分辨率质谱检测技术,共检测到 1009 种差异表达的差异代谢物。根据京都基因与基因组百科全书富集分析,SDC-1 敲除显著改变了脂肪消化和吸收、GnRH 信号通路、果糖和甘露糖代谢以及其他一些与氨基酸相关的代谢途径,并显著正向调节了长寿调控途径、长寿调控途径-线虫、烟酰胺和烟酸代谢以及维生素消化和吸收途径休克后。我们的研究结果表明,SDC-1 敲除可能通过增加烟酰胺代谢在出血性休克中具有潜在的治疗作用。