Charles Perkins Centre and School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW 2006, Australia; Neuroscience Division, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Sydney, NSW 2010, Australia.
Neuroscience Division, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Sydney, NSW 2010, Australia.
Cell Metab. 2016 Jul 12;24(1):75-90. doi: 10.1016/j.cmet.2016.06.010.
Non-nutritive sweeteners like sucralose are consumed by billions of people. While animal and human studies have demonstrated a link between synthetic sweetener consumption and metabolic dysregulation, the mechanisms responsible remain unknown. Here we use a diet supplemented with sucralose to investigate the long-term effects of sweet/energy imbalance. In flies, chronic sweet/energy imbalance promoted hyperactivity, insomnia, glucose intolerance, enhanced sweet taste perception, and a sustained increase in food and calories consumed, effects that are reversed upon sucralose removal. Mechanistically, this response was mapped to the ancient insulin, catecholamine, and NPF/NPY systems and the energy sensor AMPK, which together comprise a novel neuronal starvation response pathway. Interestingly, chronic sweet/energy imbalance promoted increased food intake in mammals as well, and this also occurs through an NPY-dependent mechanism. Together, our data show that chronic consumption of a sweet/energy imbalanced diet triggers a conserved neuronal fasting response and increases the motivation to eat.
非营养性甜味剂,如三氯蔗糖,被数十亿人食用。虽然动物和人体研究已经证明了合成甜味剂的摄入与代谢失调之间存在联系,但导致这种联系的机制尚不清楚。在这里,我们使用添加三氯蔗糖的饮食来研究甜味/能量失衡的长期影响。在果蝇中,慢性甜味/能量失衡会促进过度活跃、失眠、葡萄糖不耐受、增强对甜味的感知,并持续增加食物和卡路里的摄入,而这些影响在去除三氯蔗糖后会得到逆转。从机制上讲,这种反应可以映射到古老的胰岛素、儿茶酚胺和 NPF/NPY 系统以及能量传感器 AMPK,它们共同构成了一种新的神经元饥饿反应途径。有趣的是,慢性甜味/能量失衡也会促进哺乳动物食物摄入量的增加,而这也是通过 NPY 依赖的机制发生的。总之,我们的数据表明,慢性摄入甜味/能量失衡的饮食会引发一种保守的神经元禁食反应,并增加进食的动力。