de Beaudrap P, Witten G, Biltz G, Perrier E
Institut de Recherche et de Développement. 32, avenue Henri Varagnat, 93143 Bondy cedex, France.
J Theor Biol. 2006 Sep 7;242(1):151-63. doi: 10.1016/j.jtbi.2006.02.009. Epub 2006 Mar 30.
Fuel selection in human muscle is key to explaining insulin resistance. In obesity and type 2 diabetes mellitus, there is an increased content of lipid within and around muscle fibers. Changes in muscle fuel partitioning of lipid, between oxidation and storage of fat, contribute to the accumulation of intramuscular triglycerides and to the pathogenesis of both obesity and type 2 diabetes mellitus. A mathematical model of the aggregated metabolism in skeletal muscle was developed and the effects of fuel selection for lean and obese individuals under fasting conditions, insulin-stimulated conditions, and oscillating insulin conditions were examined. Model results were complementary to prior observations that elevated lipid oxidation during insulin-stimulated conditions is correlated with insulin resistance. The model also adequately simulated metabolic inflexibility between fat and glucose oxidation in the obese individual. A novel sensitivity analysis indicated the strong interaction effects of parameters of glucose and lipid oxidation pathways on the variables of each pathway.
人体肌肉中的燃料选择是解释胰岛素抵抗的关键。在肥胖和2型糖尿病中,肌肉纤维内部及周围的脂质含量增加。肌肉中脂质在氧化和储存之间的燃料分配变化,会导致肌肉内甘油三酯的积累,并促成肥胖和2型糖尿病的发病机制。我们建立了一个骨骼肌聚集代谢的数学模型,并研究了在禁食条件、胰岛素刺激条件和胰岛素振荡条件下,瘦人和肥胖个体的燃料选择效应。模型结果与之前的观察结果相辅相成,即在胰岛素刺激条件下脂质氧化升高与胰岛素抵抗相关。该模型还充分模拟了肥胖个体脂肪和葡萄糖氧化之间的代谢不灵活性。一项新颖的敏感性分析表明,葡萄糖和脂质氧化途径的参数对各途径变量具有强烈的相互作用效应。