Geng Chunmei, Qiao Yi, Guo Yujin, Han Wenxiu, Wu Bin, Wang Changshui, Zhang Jun, Chen Dan, Yang Mengqi, Jiang Pei
Institute of Clinical Pharmacy & Pharmacology, Jining First People's Hospital, Jining Medical University, Jining 272011, China.
Department of Public Health, Jining Medical University, Jining 272011, China.
Ann Transl Med. 2019 Dec;7(23):781. doi: 10.21037/atm.2019.11.21.
Prolonged exposure to stress triggers depression, threatening human health. Thus, to thoroughly understand the underlying pathophysiologic mechanism of chronic unpredictable mild stress (CUMS)-induced depression is urgently needed. Ultra-high-performance liquid chromatography-mass spectroscopy (UPLC-MS)-based lipidomic and metabolomic approaches has been used for discovering metabolite biomarkers to develop new diagnostic and therapeutic means. Thus, our study aimed to conduct integrated metabolomics and lipidomics to identify metabolites and lipids biomarkers in the hippocampus in rat models of CUMS-induced depression.
Twelve eight-week-old male Sprague-Dawley rats (weight 210±30 g) were randomly distributed to one of the following two groups (n=6): control or CUMS. Established UPLC-MS-based lipidomic and metabolomic approaches were used to determine the metabolites and lipids in the hippocampus of rats. SICMA-P and GraphPad software were performed to discover potential metabolites and lipids biomarkers in the hippocampus of rats between the two groups.
A total of 35 potential metabolites and 171 lipids were identified and found to be mainly related to amino acid and lipid metabolism. These metabolites were involved in different metabolic pathways and connected to each other, which might participate in the occurrence and development of depression.
Our findings underlined the metabolites, lipids and metabolic pathways that were changed in the hippocampus in CUMS compared to the controls, providing novel insights in the metabolism in the hippocampus of rats and revealing the new lipid-related targets.
长期暴露于应激会引发抑郁症,威胁人类健康。因此,迫切需要深入了解慢性不可预测轻度应激(CUMS)诱导的抑郁症的潜在病理生理机制。基于超高效液相色谱-质谱联用(UPLC-MS)的脂质组学和代谢组学方法已被用于发现代谢物生物标志物,以开发新的诊断和治疗手段。因此,我们的研究旨在进行综合代谢组学和脂质组学研究,以鉴定CUMS诱导的抑郁症大鼠模型海马体中的代谢物和脂质生物标志物。
将12只8周龄雄性Sprague-Dawley大鼠(体重210±30 g)随机分为以下两组之一(n = 6):对照组或CUMS组。采用基于UPLC-MS的脂质组学和代谢组学方法测定大鼠海马体中的代谢物和脂质。使用SICMA-P和GraphPad软件发现两组大鼠海马体中潜在的代谢物和脂质生物标志物。
共鉴定出35种潜在代谢物和171种脂质,发现它们主要与氨基酸和脂质代谢有关。这些代谢物参与不同的代谢途径并相互关联,可能参与抑郁症的发生和发展。
我们的研究结果强调了与对照组相比,CUMS大鼠海马体中发生变化的代谢物、脂质和代谢途径,为大鼠海马体的代谢提供了新的见解,并揭示了新的脂质相关靶点。