van Sloun Bart, Goossens Gijs H, Erdõs Balázs, O'Donovan Shauna D, Singh-Povel Cécile M, Geurts Jan M W, van Riel Natal A W, Arts Ilja C W
TiFN, Wageningen, the Netherlands.
Maastricht Centre for Systems Biology (MaCSBio), Maastricht University, Maastricht, the Netherlands.
iScience. 2023 Feb 18;26(3):106218. doi: 10.1016/j.isci.2023.106218. eCollection 2023 Mar 17.
Current computational models of whole-body glucose homeostasis describe physiological processes by which insulin regulates circulating glucose concentrations. While these models perform well in response to oral glucose challenges, interaction with other nutrients that impact postprandial glucose metabolism, such as amino acids (AAs), is not considered. Here, we developed a computational model of the human glucose-insulin system, which incorporates the effects of AAs on insulin secretion and hepatic glucose production. This model was applied to postprandial glucose and insulin time-series data following different AA challenges (with and without co-ingestion of glucose), dried milk protein ingredients, and dairy products. Our findings demonstrate that this model allows accurate description of postprandial glucose and insulin dynamics and provides insight into the physiological processes underlying meal responses. This model may facilitate the development of computational models that describe glucose homeostasis following the intake of multiple macronutrients, while capturing relevant features of an individual's metabolic health.
当前全身葡萄糖稳态的计算模型描述了胰岛素调节循环葡萄糖浓度的生理过程。虽然这些模型在应对口服葡萄糖挑战时表现良好,但未考虑与影响餐后葡萄糖代谢的其他营养素(如氨基酸)的相互作用。在此,我们开发了一种人类葡萄糖 - 胰岛素系统的计算模型,该模型纳入了氨基酸对胰岛素分泌和肝脏葡萄糖生成的影响。此模型应用于不同氨基酸挑战(有或无葡萄糖共同摄入)、干乳蛋白成分和乳制品后的餐后葡萄糖和胰岛素时间序列数据。我们的研究结果表明,该模型能够准确描述餐后葡萄糖和胰岛素动态,并深入了解餐后反应背后的生理过程。该模型可能有助于开发描述多种宏量营养素摄入后葡萄糖稳态的计算模型,同时捕捉个体代谢健康的相关特征。