MRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK; Institute of Clinical Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UK.
Institute for Experimental Medicine, Kiel University, 24105 Kiel, Germany.
Cell Metab. 2020 Apr 7;31(4):710-725.e7. doi: 10.1016/j.cmet.2020.02.016. Epub 2020 Mar 19.
High-sugar diets cause thirst, obesity, and metabolic dysregulation, leading to diseases including type 2 diabetes and shortened lifespan. However, the impact of obesity and water imbalance on health and survival is complex and difficult to disentangle. Here, we show that high sugar induces dehydration in adult Drosophila, and water supplementation fully rescues their lifespan. Conversely, the metabolic defects are water-independent, showing uncoupling between sugar-induced obesity and insulin resistance with reduced survival in vivo. High-sugar diets promote accumulation of uric acid, an end-product of purine catabolism, and the formation of renal stones, a process aggravated by dehydration and physiological acidification. Importantly, regulating uric acid production impacts on lifespan in a water-dependent manner. Furthermore, metabolomics analysis in a human cohort reveals that dietary sugar intake strongly predicts circulating purine levels. Our model explains the pathophysiology of high-sugar diets independently of obesity and insulin resistance and highlights purine metabolism as a pro-longevity target.
高糖饮食会导致口渴、肥胖和代谢失调,从而引发 2 型糖尿病和寿命缩短等疾病。然而,肥胖和水失衡对健康和生存的影响是复杂的,难以理清。在这里,我们表明高糖会导致成年果蝇脱水,而水的补充则能完全挽救它们的寿命。相反,代谢缺陷与水无关,表明高糖诱导的肥胖和胰岛素抵抗与体内生存能力下降之间存在解偶联。高糖饮食会促进尿酸(嘌呤代谢的终产物)的积累和肾结石的形成,而脱水和生理酸化会加剧这一过程。重要的是,尿酸生成的调节会以依赖水的方式影响寿命。此外,在人类队列中的代谢组学分析表明,饮食中的糖摄入量强烈预测循环嘌呤水平。我们的模型独立于肥胖和胰岛素抵抗解释了高糖饮食的病理生理学,并强调了嘌呤代谢作为一种长寿目标。