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饮食诱导肥胖小鼠模型和糖尿病个体中的代谢物谱分析:质谱和质子核磁共振光谱联用研究

Metabolite Profiling in a Diet-Induced Obesity Mouse Model and Individuals with Diabetes: A Combined Mass Spectrometry and Proton Nuclear Magnetic Resonance Spectroscopy Study.

作者信息

Vieira João P P, Ottosson Filip, Jujic Amra, Denisov Vladimir, Magnusson Martin, Melander Olle, Duarte João M N

机构信息

Department of Experimental Medical Science, Faculty of Medicine, Lund University, 22184 Lund, Sweden.

Wallenberg Centre for Molecular Medicine, Lund University, 22100 Lund, Sweden.

出版信息

Metabolites. 2023 Jul 23;13(7):874. doi: 10.3390/metabo13070874.

Abstract

Mass spectrometry (MS) and nuclear magnetic resonance (NMR) spectroscopy techniques have been used extensively for metabolite profiling. Although combining these two analytical modalities has the potential of enhancing metabolite coverage, such studies are sparse. In this study we test the hypothesis that combining the metabolic information obtained using liquid chromatography (LC) MS and H NMR spectroscopy improves the discrimination of metabolic disease development. We induced metabolic syndrome in male mice using a high-fat diet (HFD) exposure and performed LC-MS and NMR spectroscopy on plasma samples collected after 1 and 8 weeks of dietary intervention. In an orthogonal projection to latent structures (OPLS) analysis, we observed that combining MS and NMR was stronger than each analytical method alone at determining effects of both HFD feeding and time-on-diet. We then tested our metabolomics approach on plasma from 56 individuals from the Malmö Diet and Cancer Study (MDCS) cohort. All metabolic pathways impacted by HFD feeding in mice were confirmed to be affected by diabetes in the MDCS cohort, and most prominent HFD-induced metabolite concentration changes in mice were also associated with metabolic syndrome parameters in humans. The main drivers of metabolic disease discrimination emanating from the present study included plasma levels of xanthine, hippurate, 2-hydroxyisovalerate, S-adenosylhomocysteine and dimethylguanidino valeric acid. In conclusion, our combined NMR-MS approach provided a snapshot of metabolic imbalances in humans and a mouse model, which was improved over employment of each analytical method alone.

摘要

质谱(MS)和核磁共振(NMR)光谱技术已被广泛用于代谢物谱分析。尽管将这两种分析方式结合起来有可能提高代谢物覆盖率,但此类研究却很少见。在本研究中,我们检验了这样一个假设,即结合使用液相色谱(LC)-MS和1H NMR光谱获得的代谢信息可改善对代谢性疾病发展的辨别。我们通过高脂饮食(HFD)诱导雄性小鼠发生代谢综合征,并对饮食干预1周和8周后采集的血浆样本进行LC-MS和NMR光谱分析。在正交投影到潜在结构(OPLS)分析中,我们观察到,在确定HFD喂养和饮食时间的影响方面,将MS和NMR结合起来比单独使用每种分析方法的效果更强。然后,我们在来自马尔默饮食与癌症研究(MDCS)队列的56名个体的血浆上测试了我们的代谢组学方法。在小鼠中受HFD喂养影响的所有代谢途径在MDCS队列中均被证实受糖尿病影响,并且在小鼠中最显著的HFD诱导的代谢物浓度变化也与人类的代谢综合征参数相关。本研究中代谢疾病辨别的主要驱动因素包括黄嘌呤、马尿酸盐、2-羟基异戊酸、S-腺苷同型半胱氨酸和二甲基胍基戊酸的血浆水平。总之,我们的NMR-MS联合方法提供了人类和小鼠模型中代谢失衡的概况,相较于单独使用每种分析方法有了改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab84/10385288/736439de6d88/metabolites-13-00874-g001.jpg

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