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首页> 外文期刊>PLoS Computational Biology >Quantifying the Contribution of the Liver to Glucose Homeostasis: A Detailed Kinetic Model of Human Hepatic Glucose Metabolism
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Quantifying the Contribution of the Liver to Glucose Homeostasis: A Detailed Kinetic Model of Human Hepatic Glucose Metabolism

机译:量化肝脏对葡萄糖稳态的贡献:人类肝葡萄糖代谢的详细动力学模型。

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Despite the crucial role of the liver in glucose homeostasis, a detailed mathematical model of human hepatic glucose metabolism is lacking so far. Here we present a detailed kinetic model of glycolysis, gluconeogenesis and glycogen metabolism in human hepatocytes integrated with the hormonal control of these pathways by insulin, glucagon and epinephrine. Model simulations are in good agreement with experimental data on (i) the quantitative contributions of glycolysis, gluconeogenesis, and glycogen metabolism to hepatic glucose production and hepatic glucose utilization under varying physiological states. (ii) the time courses of postprandial glycogen storage as well as glycogen depletion in overnight fasting and short term fasting (iii) the switch from net hepatic glucose production under hypoglycemia to net hepatic glucose utilization under hyperglycemia essential for glucose homeostasis (iv) hormone perturbations of hepatic glucose metabolism. Response analysis reveals an extra high capacity of the liver to counteract changes of plasma glucose level below 5 mM (hypoglycemia) and above 7.5 mM (hyperglycemia). Our model may serve as an important module of a whole-body model of human glucose metabolism and as a valuable tool for understanding the role of the liver in glucose homeostasis under normal conditions and in diseases like diabetes or glycogen storage diseases.
机译:尽管肝脏在葡萄糖稳态中起着至关重要的作用,但到目前为止,尚缺乏人类肝葡萄糖代谢的详细数学模型。在这里,我们提出了人类肝细胞中糖酵解,糖异生和糖原代谢的详细动力学模型,并结合了胰岛素,胰高血糖素和肾上腺素对这些途径的激素控制。模型模拟与(i)在不同生理状态下糖酵解,糖异生和糖原代谢对肝葡萄糖生成和肝葡萄糖利用的定量贡献与实验数据高度吻合。 (ii)过夜禁食和短期禁食后餐后糖原存储的时间过程以及糖原耗竭的时间过程(iii)从低血糖下的净肝葡萄糖产生切换为葡萄糖稳态所需的高血糖下的净肝葡萄糖利用(iv)激素扰动肝葡萄糖代谢。响应分析显示,肝脏具有超高的能力来抵消低于5 mM(低血糖)和高于7.5 mM(高血糖)的血浆葡萄糖水平的变化。我们的模型可作为人体葡萄糖代谢全身模型的重要模块,并可作为了解肝脏在正常条件下以及在糖尿病或糖原贮积病等疾病中葡萄糖稳态中作用的重要工具。

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