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Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction

机译:应激敏感大鼠肠脑轴功能障碍模型的代谢组和微生物组分析

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摘要

Stress negatively impacts gut and brain health. Individual differences in response to stress have been linked to genetic and environmental factors and more recently, a role for the gut microbiota in the regulation of stress-related changes has been demonstrated. However, the mechanisms by which these factors influence each other are poorly understood, and there are currently no established robust biomarkers of stress susceptibility. To determine the metabolic and microbial signatures underpinning physiological stress responses, we compared stress-sensitive Wistar Kyoto (WKY) rats to the normo-anxious Sprague Dawley (SD) strain. Here we report that acute stress-induced strain-specific changes in brain lipid metabolites were a prominent feature in WKY rats. The relative abundance of Lactococcus correlated with the relative proportions of many brain lipids. In contrast, plasma lipids were significantly elevated in response to stress in SD rats, but not in WKY rats. Supporting these findings, we found that the greatest difference between the SD and WKY microbiomes were the predicted relative abundance of microbial genes involved in lipid and energy metabolism. Our results provide potential insights for developing novel biomarkers of stress vulnerability, some of which appear genotype specific.
机译:压力会对肠道和大脑健康产生负面影响。个体对压力反应的差异与遗传和环境因素有关,最近,肠道菌群在调节压力相关变化中的作用已得到证实。但是,这些因素相互影响的机制了解甚少,目前还没有建立明确的应激敏感性生物标记。为了确定支撑生理应激反应的代谢和微生物特征,我们将应激敏感的Wistar Kyoto(WKY)大鼠与正常焦虑的Sprague Dawley(SD)菌株进行了比较。在这里,我们报告说,急性应激诱导的脑脂质代谢产物的菌株特异性变化是WKY大鼠的显着特征。乳酸球菌的相对丰度与许多脑脂质的相对比例相关。相反,在SD大鼠中,血浆脂质响应压力而明显升高,但在WKY大鼠中却没有。支持这些发现,我们发现SD和WKY微生物组之间的最大差异是参与脂质和能量代谢的微生物基因的预测相对丰度。我们的结果为开发压力脆弱性的新生物标志物提供了潜在的见识,其中一些生物标志物似乎是基因型特异性的。

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