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On a Novel, Simplified Model Framework Describing Ascorbic Acid Concentration Dynamics

机译:关于描述抗坏血酸浓度动力学的新型简化模型框架

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Ascorbic acid is an essential aminoacid which interacts in several parts of the human body metabolism. The ascorbic acid concentration is controlled by homeostasis, a biological, autonomous control function in the body. Humans are not able to produce ascorbic acid, and the ascorbic acid concentration is maintained by daily oral digestion. Ascorbic acid is buffered in various tissues, such as the adrenal glands, brain, muscles, and other. Excessive ascorbic acid is extracted from the body through urine and intestines. Measuring ascorbic acid concentration in the body is challenging, and special procedures must be followed when extracting a blood sample and performing a concentration analysis. This paper presents a novel, simplified model framework of the ascorbic acid homeostasis in the human body plasma and tissues, including tissues such as adrenal glands, brain, liver, muscles and bone marrow. These tissues also act as ascorbic acid concentration buffers, in case of low oral supply. The dynamic model framework is based on mass balances of ascorbate acid in various tissues, including tissue buffer terms involving the intestine, kidney, adrenal glands, and other critical and noncritical tissues. The interaction between buffer tissues and fluids is maintained by the body homeostasis using chemical transport protein molecules. Additional usage terms describing energy metabolism, body growth, and immune system response are also included. This dynamic model framework, including the ascorbic acid concentration control system, is simulated with assumed parameters based on available literature. The results indicates that further investigations using experiments, in addition to adaptive model parameter estimation schemes and additional model verification tests are needed in order to identify the various model framework parameters to fit the human body ascorbic acid homeostasis and pharmacokinetics.
机译:抗坏血酸是一种必不可少的氨基酸,它在人体新陈代谢的几个部分中相互作用。抗坏血酸的浓度由体内动态平衡机制控制。人类无法产生抗坏血酸,并且每天口服消化可维持抗坏血酸的浓度。抗坏血酸在各种组织(如肾上腺,大脑,肌肉等)中得到缓冲。过量的抗坏血酸是通过尿液和肠道从体内提取的。测量体内抗坏血酸的浓度具有挑战性,并且在提取血液样本并进行浓度分析时必须遵循特殊的程序。本文提出了一种新颖,简化的人体血浆和组织(包括肾上腺,脑,肝,肌肉和骨髓等组织)中抗坏血酸稳态的模型框架。在口服供应不足的情况下,这些组织还充当抗坏血酸浓度的缓冲剂。动态模型框架基于各种组织中抗坏血酸的质量平衡,包括涉及肠,肾,肾上腺和其他关键和非关键组织的组织缓冲液术语。缓冲组织和液体之间的相互作用通过使用化学转运蛋白分子的体内稳态得以维持。还包括描述能量代谢,身体生长和免疫系统反应的其他使用条款。该动态模型框架(包括抗坏血酸浓度控制系统)是根据现有文献使用假定参数进行模拟的。结果表明,除了自适应模型参数估计方案和其他模型验证测试之外,还需要通过实验进行进一步研究,以便确定各种模型框架参数以适应人体抗坏血酸的体内稳态和药代动力学。

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