Internal Medicine Department, Faculty of Medical Sciences, FCM, UNICAMP, Campinas, SP, Brazil.
Mediators Inflamm. 2013;2013:986734. doi: 10.1155/2013/986734. Epub 2013 Jun 12.
Obesity is the main condition that is correlated with the appearance of insulin resistance, which is the major link among its comorbidities, such as type 2 diabetes, nonalcoholic fatty liver disease, cardiovascular and neurodegenerative diseases, and several types of cancer. Obesity affects a large number of individuals worldwide; it degrades human health and quality of life. Here, we review the role of the gut microbiota in the pathophysiology of obesity and type 2 diabetes, which is promoted by a bacterial diversity shift mediated by overnutrition. Whole bacteria, their products, and metabolites undergo increased translocation through the gut epithelium to the circulation due to degraded tight junctions and the consequent increase in intestinal permeability that culminates in inflammation and insulin resistance. Several strategies focusing on modulation of the gut microbiota (antibiotics, probiotics, and prebiotics) are being experimentally employed in metabolic derangement in order to reduce intestinal permeability, increase the production of short chain fatty acids and anorectic gut hormones, and promote insulin sensitivity to counteract the inflammatory status and insulin resistance found in obese individuals.
肥胖是与胰岛素抵抗出现相关的主要病症,而胰岛素抵抗是 2 型糖尿病、非酒精性脂肪性肝病、心血管和神经退行性疾病以及多种癌症等合并症的主要环节。肥胖影响着全球大量人群;它降低了人类健康和生活质量。在这里,我们综述了肠道微生物组在肥胖和 2 型糖尿病的病理生理学中的作用,这种作用是由营养过剩引起的细菌多样性变化所推动的。由于紧密连接被破坏以及随之而来的肠道通透性增加,导致整个细菌及其产物和代谢物穿过肠上皮细胞向循环中更多地转移,最终导致炎症和胰岛素抵抗。几种专注于调节肠道微生物组的策略(抗生素、益生菌和益生元)正在被实验性地应用于代谢紊乱中,以降低肠道通透性,增加短链脂肪酸和厌食性肠道激素的产生,并促进胰岛素敏感性,以对抗肥胖个体中存在的炎症状态和胰岛素抵抗。