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Metabolite identification in fecal microbiota transplantation mouse livers and combined proteomics with chronic unpredictive mild stress mouse livers

机译:粪便微生物群移植小鼠肝脏中代谢物的鉴定以及蛋白质组学与慢性不可预测的轻度应激小鼠肝脏的结合

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Major depressive disorder (MDD) is a common mood disorder. Gut microbiota may be involved in the pathogenesis of depression via the microbe–gut–brain axis. Liver is vulnerable to exposure of bacterial products translocated from the gut via the portal vein and may be involved in the axis. In this study, germ-free mice underwent fecal microbiota transplantation from MDD patients and healthy controls. Behavioral tests verified the depression model. Metabolomics using gas chromatography–mass spectrometry, nuclear magnetic resonance, and liquid chromatography–mass spectrometry determined the influence of microbes on liver metabolism. With multivariate statistical analysis, 191 metabolites were distinguishable in MDD mice from control (CON) mice. Compared with CON mice, MDD mice showed lower levels for 106 metabolites and higher levels for 85 metabolites. These metabolites are associated with lipid and energy metabolism and oxidative stress. Combined analyses of significantly changed proteins in livers from another depression model induced by chronic unpredictive mild stress returned a high score for the Lipid Metabolism, Free Radical Scavenging, and Molecule Transports network, and canonical pathways were involved in energy metabolism and tryptophan degradation. The two mouse models of depression suggest that changes in liver metabolism might be involved in the pathogenesis of MDD. Conjoint analyses of fecal, serum, liver, and hippocampal metabolites from fecal microbiota transplantation mice suggested that aminoacyl-tRNA biosynthesis significantly changed and fecal metabolites showed a close relationship with the liver. These findings may help determine the biological mechanisms of depression and provide evidence about “depression microbes” impacting on liver metabolism.
机译:重度抑郁症(MDD)是一种常见的情绪障碍。肠道菌群可能通过微生物-肠-脑轴参与了抑郁症的发病机制。肝脏很容易暴露通过门静脉从肠道转移而来的细菌,并且可能累及轴。在这项研究中,无菌小鼠接受了MDD患者和健康对照组的粪便微生物群移植。行为测试验证了抑郁模型。使用气相色谱-质谱,核磁共振和液相色谱-质谱的代谢组学确定了微生物对肝脏代谢的影响。通过多变量统计分析,在MDD小鼠中有191种代谢物与对照(CON)小鼠相区别。与CON小鼠相比,MDD小鼠的106种代谢物含量较低,而85种代谢物含量较高。这些代谢物与脂质和能量代谢以及氧化应激有关。对慢性不可预测的轻度压力诱发的另一种抑郁症模型中的肝脏中显着变化的蛋白质进行的综合分析,在脂质代谢,自由基清除和分子转运网络方面获得了高分,并且经典途径参与了能量代谢和色氨酸降解。两种抑郁症小鼠模型表明,肝脏代谢的变化可能与MDD的发病机理有关。粪便微生物群移植小鼠的粪便,血清,肝脏和海马代谢产物的联合分析表明,氨酰-tRNA的生物合成发生了显着变化,粪便代谢产物与肝脏之间存在密切的关系。这些发现可能有助于确定抑郁症的生物学机制,并提供有关“抑郁症微生物”影响肝脏代谢的证据。

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