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Exercise training-induced! modification of the gut microbiota persists after microbiota colonization and attenuates the response to chemically-induced colitis in gnotobiotic mice

机译:运动培训诱导! 微生物群殖民化后肠道微生物的修饰持续,并衰减肾病小鼠中的化学诱导的结肠炎的响应

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Exercise reduces the risk of inflammatory disease by modulating a variety of tissue and cell types, including those within the gastrointestinal tract. Recent data indicates that exercise can also alter the gut microbiota, but little is known as to whether these changes affect host function. Here, we use a germ-free (GF) animal model to test whether exercise-induced modifications in the gut microbiota can directly affect host responses to microbiota colonization and chemically-induced colitis. Donor mice (n = 19) received access to a running wheel (n = 10) or remained without access (n = 9) for a period of six weeks. After euthanasia, cecal contents were pooled by activity treatment and transplanted into two separate cohorts of GF mice. Two experiments were then conducted. First, mice were euthanized five weeks after the microbiota transplant and tissues were collected for analysis. A second cohort of GF mice were colonized by donor microbiotas for four weeks before dextran-sodium-sulfate was administered to induce acute colitis, after which mice were euthanized for tissue analysis. We observed that microbial transplants from donor (exercised or control) mice led to differences in microbiota β-diversity, metabolite profiles, colon inflammation, and body mass in recipient mice five weeks after colonization, We also demonstrate that colonization of mice with a gut microbiota from exercise-trained mice led to an attenuated response to chemical colitis, evidenced by reduced colon shortening, attenuated mucus depletion and augmented expression of cytokines involved in tissue regeneration. Exercise-induced modifications in the gut microbiota can mediate host-microbial interactions with potentially beneficial outcomes for the host.
机译:通过调节各种组织和细胞类型,锻炼降低炎症疾病的风险,包括胃肠道内的组织和细胞类型。最近的数据表明,锻炼也可以改变肠道微生物群,但很少称这些变化是否会影响主机函数。在这里,我们使用无菌(GF)动物模型来测试肠道微生物的运动诱导的修饰是否可以直接影响对微生物群殖民化和化学诱导的结肠炎的宿主反应。供体小鼠(n = 19)接收到运行轮(n = 10)的访问,或者在六周内没有访问(n = 9)。在安乐死后,通过活性处理合并螯合含量并移植成两个单独的GF小鼠的群体。然后进行两种实验。首先,在收集微生物脂蛋白移植和组织以进行分析后,将小鼠安乐死。在给予葡聚糖 - 硫酸钠诱导急性结肠炎之前,通过供体微生物溶解的第二次GF小鼠群组群体通过供体微生物瘤焚烧四周,之后将小鼠对组织分析安乐死。我们观察到来自供体(锻炼或对照)小鼠的微生物移植导致殖民化五周内的微生物瘤β-多样性,代谢物谱,结肠炎症,结肠炎症和体重的差异,我们还证明了用肠道微生物的小鼠定植从运动训练的小鼠导致对化学结肠炎的衰减反应,通过降低的结肠缩短证明,减毒的粘液耗尽和组织再生中参与细胞因子的增强表达。肠道微生物群中的运动诱导的修饰可以介导与宿主的潜在有益结果的宿主微生物相互作用。

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