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肠道微生物群是引发肥胖、全身炎症和胰岛素抵抗的关键因素。

Gut microbiota as a key player in triggering obesity, systemic inflammation and insulin resistance.

作者信息

Escobedo Galileo, López-Ortiz Eduardo, Torres-Castro Israel

机构信息

Hospital General de México.

出版信息

Rev Invest Clin. 2014 Sep-Oct;66(5):450-9.

Abstract

Obesity-related systemic inflammation contributes to develop insulin resistance. The main factors involved in the relationship of obesity with systemic inflammation and insulin resistance have not been completely elucidated. Microbiota includes around 1013 to 1014 microbes harboring the human gut, which are clustered in approximately a thousand different bacterial species. Several studies suggest that imbalance in the intestinal bacterial population could result in obesity, systemic inflammation and metabolic dysfunction. Here, we review the main bacterial groups observed in obesity as well as their possible role in increasing the intestinal permeability and lipopolysaccharide-related endotoxemia. Furthermore, we point out the role of intestinal dysbiosis in the inflammatory activation of macrophages with the ability to infiltrate in the visceral adipose tissue and induce insulin resistance. Finally, we discuss the apparent beneficial use of prebiotics and probiotics in ameliorating both systemic inflammation and metabolic dysfunction. Present information may be useful in the future design of novel therapies focused on treating obesity and insulin resistance by restoring the gut microbiota balance.

摘要

肥胖相关的全身炎症会促使胰岛素抵抗的发展。肥胖与全身炎症及胰岛素抵抗之间关系所涉及的主要因素尚未完全阐明。微生物群包括栖息在人类肠道中的约10¹³至10¹⁴个微生物,它们聚集在大约一千种不同的细菌物种中。多项研究表明,肠道细菌种群失衡可能导致肥胖、全身炎症和代谢功能障碍。在此,我们综述了在肥胖中观察到的主要细菌群体及其在增加肠道通透性和脂多糖相关内毒素血症方面可能发挥的作用。此外,我们指出肠道微生物群失调在巨噬细胞炎症激活中的作用,这些巨噬细胞能够浸润内脏脂肪组织并诱导胰岛素抵抗。最后,我们讨论了益生元和益生菌在改善全身炎症和代谢功能障碍方面明显的有益作用。目前的信息可能有助于未来设计新的疗法,通过恢复肠道微生物群平衡来治疗肥胖和胰岛素抵抗。

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