Unitat de Recerca Biomèdica, Hospital Universitari Sant Joan, Institut d'Investigació Sanitària Pere Virgili, Universitat Rovira i Virgili, 43201 Reus, Spain.
Centro de Investigaciones Biológicas (CIB-CSIC), 28040 Madrid, Spain.
Int J Mol Sci. 2017 Oct 28;18(11):2263. doi: 10.3390/ijms18112263.
Prevention of the metabolic consequences of a chronic energy-dense/high-fat diet (HFD) represents a public health priority. Metformin is a strong candidate to be incorporated in alternative therapeutic approaches. We used a targeted metabolomic approach to assess changes related to the multi-faceted metabolic disturbances provoked by HFD. We evaluated the protective effects of metformin and explored how pro-inflammatory and metabolic changes respond when mice rendered obese, glucose-intolerant and hyperlipidemic were switched to diet reversal with or without metformin. Mice treated with metformin and diet-reversal showed a dramatically improved protection against HFD-induced hepatic steatosis, a beneficial effect that was accompanied by a lowering of liver-infiltrating pro-inflammatory macrophages and lower release of pro-inflammatory cytokines. Metformin combined with diet reversal promoted effective weight loss along with better glucose control, lowered levels of circulating cholesterol and triglycerides, and reduced adipose tissue content. Our findings underscored the ability of metformin to target the contribution of branched chain amino acids to adipose tissue metabolism while suppressing mitochondrial-dependent biosynthesis in hepatic tissue. The relationship between adipose tissue and liver might provide clinical potential for combining metformin and dietary modifications to protect against the metabolic damage occurring upon excessive dietary fat intake.
预防慢性高能量/高脂肪饮食(HFD)引起的代谢后果是公共卫生的重点。二甲双胍是一种很有前途的候选药物,可以纳入替代治疗方法。我们使用靶向代谢组学方法来评估与 HFD 引起的多种代谢紊乱相关的变化。我们评估了二甲双胍的保护作用,并探讨了当肥胖、葡萄糖不耐受和高脂血症的小鼠转为逆转饮食时,炎症和代谢变化如何反应,以及是否使用二甲双胍。用二甲双胍和饮食逆转治疗的小鼠对 HFD 引起的肝脂肪变性有明显的保护作用,这种有益的作用伴随着肝内浸润的促炎巨噬细胞减少和促炎细胞因子释放减少。二甲双胍联合饮食逆转不仅促进了有效的体重减轻,还改善了血糖控制,降低了循环胆固醇和甘油三酯水平,并减少了脂肪组织含量。我们的研究结果强调了二甲双胍靶向支链氨基酸对脂肪组织代谢的贡献,同时抑制肝组织中依赖线粒体的生物合成的能力。脂肪组织和肝脏之间的关系可能为联合使用二甲双胍和饮食改变以预防过度饮食脂肪摄入引起的代谢损伤提供临床潜力。