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Linking intestinal homeostasis and liver disease

机译:连接肠道稳态和肝病

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PURPOSE OF REVIEW: Interactions of the gut microbiome with the host are important in health and disease. Microbial translocation releases bacterial products that play a key role in progression of chronic liver disease by promoting hepatic injury and inflammation. Although this has long been recognized, we are just beginning to understand the circumstances under which the gut becomes leaky and to discover bacterial metabolites that promote liver disease. In this review, we will summarize recent findings from the last 2 years. RECENT FINDINGS: Chronic liver disease is associated with an altered microbiome with both qualitative (dysbiosis) and quantitative (overgrowth) differences. This can be viewed as a loss of the symbiotic relationship between the microflora and the host. An imbalanced intestinal homeostasis results in a breach of the gut barrier and subsequent microbial translocation. However, the contribution of the intestinal microflora is beyond simple microbial translocation as a pathogenic factor. Bacterial metabolites resulting from an imbalanced homeostasis and dysbiosis play also a crucial role in liver disease. SUMMARY: A combination between an initiating liver insult and a disturbance of the gut-host symbiosis synergize in progression of liver disease.
机译:审查目的:肠道微生物组与宿主的相互作用在健康和疾病中都很重要。微生物易位释放通过促进肝损伤和炎症来发挥慢性肝病的进展中发挥关键作用的细菌产品。虽然这已经很久得到了认可,但我们刚刚开始了解肠道变得疏忽的情况,并发现促进肝病的细菌代谢物。在本次审查中,我们将从过去2年中总结最近的结果。最近的发现:慢性肝病与具有定性(困难)和定量(过度生长)差异的改变的微生物组有关。这可以被视为微氟氯和宿主之间的共生关系的丧失。不平衡的肠道稳态导致突破肠道屏障和随后的微生物易位。然而,肠道微生物的贡献超出了简单的微生物易位作为致病因子。由不平衡的稳态和脱敏病引起的细菌代谢物也发挥着肝脏疾病的至关重要作用。概述:启动肝脏损伤与肠道 - 宿主共生的干扰之间的组合在肝病的进展中协同增量。

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