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糖尿病、肥胖与肠道菌群。

Diabetes, obesity and gut microbiota.

机构信息

Université catholique de Louvain, WELBIO (Walloon Excellence in Life sciences and BIOtechnology), Louvain Drug Research Institute, Metabolism and Nutrition Research Group, Av. E. Mounier, 73 Box B1.73.11, B-1200 Brussels, Belgium.

出版信息

Best Pract Res Clin Gastroenterol. 2013 Feb;27(1):73-83. doi: 10.1016/j.bpg.2013.03.007.

Abstract

The gut microbiota composition has been associated with several hallmarks of metabolic syndrome (e.g., obesity, type 2 diabetes, cardiovascular diseases, and non-alcoholic steatohepatitis). Growing evidence suggests that gut microbes contribute to the onset of the low-grade inflammation characterising these metabolic disorders via mechanisms associated with gut barrier dysfunctions. Recently, enteroendocrine cells and the endocannabinoid system have been shown to control gut permeability and metabolic endotoxaemia. Moreover, targeted nutritional interventions using non-digestible carbohydrates with prebiotic properties have shown promising results in pre-clinical studies in this context, although human intervention studies warrant further investigations. Thus, in this review, we discuss putative mechanisms linking gut microbiota and type 2 diabetes. These data underline the advantage of investigating and changing the gut microbiota as a therapeutic target in the context of obesity and type 2 diabetes.

摘要

肠道微生物群落的组成与多种代谢综合征的特征有关(例如肥胖、2 型糖尿病、心血管疾病和非酒精性脂肪性肝炎)。越来越多的证据表明,肠道微生物通过与肠道屏障功能障碍相关的机制,有助于这些代谢紊乱的低度炎症的发生。最近,肠内分泌细胞和内源性大麻素系统已被证明可以控制肠道通透性和代谢性内毒素血症。此外,在这方面的临床前研究中,使用具有益生元特性的不可消化碳水化合物进行靶向营养干预已显示出有希望的结果,尽管需要进一步的人体干预研究。因此,在这篇综述中,我们讨论了将肠道微生物群与 2 型糖尿病联系起来的假设机制。这些数据强调了在肥胖和 2 型糖尿病的背景下,将肠道微生物群作为治疗靶点进行研究和改变的优势。

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