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Distinct actions of the fermented beverage kefir on host behaviour, immunity and microbiome gut-brain modules in the mouse

机译:发酵饮料kefir对小鼠中宿主行为,免疫和微生物血管脑模块的不同作用

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Mounting evidence suggests a role for the gut microbiota in modulating brain physiology and behaviour, through bi-directional communication, along the gut-brain axis. As such, the gut microbiota represents a potential therapeutic target for influencing centrally mediated events and host behaviour. It is thus notable that the fermented milk beverage kefir has recently been shown to modulate the composition of the gut microbiota in mice. It is unclear whether kefirs have differential effects on microbiota-gut-brain axis and whether they can modulate host behaviour per se. To address this, two distinct kefirs (Fr1 and UK4), or unfermented milk control, were administered to mice that underwent a battery of tests to characterise their behavioural phenotype. In addition, shotgun metagenomic sequencing of ileal, caecal and faecal matter was performed, as was faecal metabolome analysis. Finally, systemic immunity measures and gut serotonin levels were assessed. Statistical analyses were performed by ANOVA followed by Dunnett's post hoc test or Kruskal-Wallis test followed by Mann-Whitney U test. Fr1 ameliorated the stress-induced decrease in serotonergic signalling in the colon and reward-seeking behaviour in the saccharin preference test. On the other hand, UK4 decreased repetitive behaviour and ameliorated stress-induced deficits in reward-seeking behaviour. Furthermore, UK4 increased fear-dependent contextual memory, yet decreased milk gavage-induced improvements in?long-term spatial learning. In the peripheral immune system, UK4 increased the prevalence of Treg cells and interleukin 10 levels, whereas Fr1 ameliorated the milk gavage stress-induced elevation in neutrophil levels and CXCL1 levels. Analysis of the gut microbiota revealed that both kefirs significantly changed the composition and functional capacity of the host microbiota, where specific bacterial species were changed in a kefir-dependent manner. Furthermore, both kefirs increased the capacity of the gut microbiota to produce GABA, which was linked to an increased prevalence in Lactobacillus reuteri. Altogether, these data show that kefir can signal through the microbiota-gut-immune-brain axis and modulate host behaviour. In addition, different kefirs may direct the microbiota toward distinct immunological and behavioural modulatory effects. These results indicate that kefir can positively modulate specific aspects of the microbiota-gut-brain axis and support the broadening of the definition of psychobiotic to include kefir fermented foods.
机译:安装证据表明肠道微生物群在调节脑生理学和行为,通过双向通信沿着肠脑轴来调节脑生理学和行为的作用。因此,肠道微生物A代表了影响中心介导的事件和宿主行为的潜在治疗靶标。因此,值得注意的是,发酵的乳饮料Kefir最近已被证明是调节小鼠中肠道微生物的组成。目前尚不清楚Kefirs是否对微生物液 - 肠轴轴具有差异影响,以及它们是否可以调节宿主行为本身。为了解决这一点,将两个不同的KEFIR(FR1和UK4)或未发酵的牛奶控制施用于经历一部分测试的小鼠,以表征其行为表型。此外,患有嗜睡剂,粘颈和粪便物质的霰弹枪偏心测序,如粪便代谢分析。最后,评估了全身免疫措施和肠道血清素水平。统计分析由Anova进行,然后进行Dunnett的后HOC测试或Kruskal-Wallis测试,然后是Mann-Whitney U测试。 FR1改善了结肠中的结肠中的血清奈奈能信号传导的压力诱导的降低,并在糖精偏好测试中汲取奖励行为。另一方面,UK4减少了重复行为,并改善了奖励行为中的压力引起的赤字。此外,UK4增加了恐惧依赖性的上下文记忆,但牛奶饲料诱导的改进减少了?长期空间学习。在外周免疫系统中,UK4增加了Treg细胞和白细胞介素10水平的患病率,而FR1改善了乳汁胁迫诱导的中性粒细胞水平和CXCL1水平的升高。肠道微生物群的分析表明,凯夫尔均显着改变了宿主微生物群的组成和功能能力,其中特异性细菌物种以依赖于Kefir依赖性的方式改变。此外,Kefirs都增加了肠道微生物群生产GABA的能力,这与Lactobacillus Reuteri的流行增加有关。完全,这些数据表明,Kefir可以通过微生物肠肠 - 肠道脑轴发出信号并调节宿主行为。此外,不同的Kefirs可以将微生物群指向不同的免疫和行为调节效果。这些结果表明,Kefir可以肯定地调节微生物肿瘤脑轴的特异性方面,并支持灵活性定义的扩大,包括Kefir发酵食品。

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