Friedman M I, Tordoff M G, Ramirez I
Brain Res Bull. 1986 Dec;17(6):855-9. doi: 10.1016/0361-9230(86)90099-7.
Inhibition of glycolysis and fatty acid oxidation by combined treatment with 2-deoxyglucose (2DG) and methyl palmoxirate, or inhibition of glycolysis and lipolysis by combined treatment with 2DG and nicotonic acid synergistically increased food intake in rats. Methyl palmoxirate treatment alone increased food intake in rats fed a high-fat, but not low-fat diet. These results provide direct evidence for a mechanism in the control of food intake that integrates signals generated by the metabolism of glucose and fatty acids. In addition, they strongly indicate a role for fatty acid oxidation in the control of eating and raise the possibility that an interaction between glucose and fat metabolism underlies the link between regulation of body fat stores and short-term food intake.
联合使用2-脱氧葡萄糖(2DG)和棕榈酰肉碱治疗抑制糖酵解和脂肪酸氧化,或者联合使用2DG和烟酸治疗抑制糖酵解和脂解,均可协同增加大鼠的食物摄入量。单独使用棕榈酰肉碱治疗可增加高脂饮食而非低脂饮食大鼠的食物摄入量。这些结果为控制食物摄入量的机制提供了直接证据,该机制整合了由葡萄糖和脂肪酸代谢产生的信号。此外,它们有力地表明脂肪酸氧化在进食控制中起作用,并增加了葡萄糖和脂肪代谢之间的相互作用是身体脂肪储存调节与短期食物摄入量之间联系基础的可能性。