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首页> 外文期刊>Scientific reports. >Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization
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Cocaine Induces Inflammatory Gut Milieu by Compromising the Mucosal Barrier Integrity and Altering the Gut Microbiota Colonization

机译:可卡因通过损害粘膜屏障完整性并改变肠道微生物群殖民化来诱导炎症肠云

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Cocaine use disorder (CUD), a major health crisis, has traditionally been considered a complication of the CNS; however, it is also closely associated with malnourishment and deteriorating gut health. In light of emerging studies on the potential role of gut microbiota in neurological disorders, we sought to understand the causal association between CUD and gut dysbiosis. Using a comprehensive approach, we confirmed that cocaine administration in mice resulted in alterations of the gut microbiota. Furthermore, cocaine-mediated gut dysbiosis was associated with upregulation of proinflammatory mediators including NF-κB and IL-1β. In vivo and in vitro analyses confirmed that cocaine altered gut-barrier composition of the tight junction proteins while also impairing epithelial permeability by potentially involving the MAPK/ERK1/2 signaling. Taken together, our findings unravel a causal link between CUD, gut-barrier dysfunction and dysbiosis and set a stage for future development of supplemental strategies for the management of CUD-associated gut complications.
机译:可卡因使用障碍(CUD),一种主要的健康危机,传统上被认为是CNS的并发症;然而,它也与营养不良和恶化的肠道健康密切相关。鉴于Gut Microbiota在神经系统疾病中的潜在作用的新出现的研究,我们试图了解CUD与肠道脱泻之间的因果关系。使用综合方法,我们证实了小鼠中的可卡因管理导致肠道微生物群的改变。此外,可卡因介导的肠道功能细胞与促炎介质的上调有关,包括NF-κB和IL-1β。体内和体外分析证实,可卡因改变了紧密结蛋白的肠道阻隔组合物,同时通过潜在涉及MAPK / ERK1 / 2信号传导,还损害上皮渗透性。我们的研究结果一起揭开了CUD,肠道屏障功能障碍和消化不良之间的因果关系,并设定了未来发展的补充策略的阶段,以管理CUD相关的肠道并发症。

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