葡萄糖代谢的可扩展数学模型。第一部分:葡萄糖-胰岛素-胰高血糖素基本模型,基本条件和基本动态

Q3 Mathematics
Caleb L. Adams, D. G. Lasseigne
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引用次数: 4

摘要

摘要提出了一个强调胰岛素和胰高血糖素反调节作用的基本模型,以启动一系列旨在探索连续控制和葡萄糖代谢主要方面的模型。三乘三动力系统使用黑匣子对单位过程进行建模,如胰岛素分泌速率和胰高血糖素分泌速率对血糖浓度的依赖性。显示了基础条件对胰岛素抵抗的依赖性以及胰岛素或胰高血糖素分泌的任何缺陷。由于肝葡萄糖的过量产生在糖尿病早期就存在,因此重要的是,数学模型应该像这个说明性模型一样,通过纳入控制胰高血糖素浓度的动力学方程来解释这种影响。所有的解决方案都符合代谢过程的总体特征。检查该模型是否存在影响其有效性的显式和隐式假设,从而确定该模型的第一次扩展应考虑葡萄糖储存和储存葡萄糖的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An extensible mathematical model of glucose metabolism. Part I: the basic glucose-insulin-glucagon model, basal conditions and basic dynamics
Abstract A basic model highlighting the counter-regulatory roles of insulin and glucagon is proposed to start a series of models designed to explore continuous rein control and major aspects of glucose metabolism. The three-by-three dynamical system uses black boxes to model unit processes such as the dependencies of insulin secretion rate and the glucagon secretion rate on blood glucose concentration. The dependency of basal conditions on insulin resistance and any defects in insulin or glucagon secretion are shown. Since over-production of hepatic glucose exists early in the history of diabetes, it is important that mathematical models should account for this effect by inclusion of the dynamical equation governing glucagon concentration as this illustrative model does. All solutions are consistent with gross features of the metabolic process. The model is examined for explicit and implicit assumptions affecting its validity which determines that the first extension to the model should account for glucose storage and the release of stored glucose.
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来源期刊
Letters in Biomathematics
Letters in Biomathematics Mathematics-Statistics and Probability
CiteScore
2.00
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14 weeks
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