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A mathematical model of brain glucose homeostasis
BACKGROUND: The physiological fact that a stable level of brain glucose is more important than that of blood glucose suggests that the ultimate goal of the glucose-insulin-glucagon (GIG) regulatory system may be homeostasis of glucose concentration in the brain rather than in the circulation. METHOD...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801528/ https://www.ncbi.nlm.nih.gov/pubmed/19943948 http://dx.doi.org/10.1186/1742-4682-6-26 |
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author | Gaohua, Lu Kimura, Hidenori |
author_facet | Gaohua, Lu Kimura, Hidenori |
author_sort | Gaohua, Lu |
collection | PubMed |
description | BACKGROUND: The physiological fact that a stable level of brain glucose is more important than that of blood glucose suggests that the ultimate goal of the glucose-insulin-glucagon (GIG) regulatory system may be homeostasis of glucose concentration in the brain rather than in the circulation. METHODS: In order to demonstrate the relationship between brain glucose homeostasis and blood hyperglycemia in diabetes, a brain-oriented mathematical model was developed by considering the brain as the controlled object while the remaining body as the actuator. After approximating the body compartmentally, the concentration dynamics of glucose, as well as those of insulin and glucagon, are described in each compartment. The brain-endocrine crosstalk, which regulates blood glucose level for brain glucose homeostasis together with the peripheral interactions among glucose, insulin and glucagon, is modeled as a proportional feedback control of brain glucose. Correlated to the brain, long-term effects of psychological stress and effects of blood-brain-barrier (BBB) adaptation to dysglycemia on the generation of hyperglycemia are also taken into account in the model. RESULTS: It is shown that simulation profiles obtained from the model are qualitatively or partially quantitatively consistent with clinical data, concerning the GIG regulatory system responses to bolus glucose, stepwise and continuous glucose infusion. Simulations also revealed that both stress and BBB adaptation contribute to the generation of hyperglycemia. CONCLUSION: Simulations of the model of a healthy person under long-term severe stress demonstrated that feedback control of brain glucose concentration results in elevation of blood glucose level. In this paper, we try to suggest that hyperglycemia in diabetes may be a normal outcome of brain glucose homeostasis. |
format | Text |
id | pubmed-2801528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28015282010-01-05 A mathematical model of brain glucose homeostasis Gaohua, Lu Kimura, Hidenori Theor Biol Med Model Research BACKGROUND: The physiological fact that a stable level of brain glucose is more important than that of blood glucose suggests that the ultimate goal of the glucose-insulin-glucagon (GIG) regulatory system may be homeostasis of glucose concentration in the brain rather than in the circulation. METHODS: In order to demonstrate the relationship between brain glucose homeostasis and blood hyperglycemia in diabetes, a brain-oriented mathematical model was developed by considering the brain as the controlled object while the remaining body as the actuator. After approximating the body compartmentally, the concentration dynamics of glucose, as well as those of insulin and glucagon, are described in each compartment. The brain-endocrine crosstalk, which regulates blood glucose level for brain glucose homeostasis together with the peripheral interactions among glucose, insulin and glucagon, is modeled as a proportional feedback control of brain glucose. Correlated to the brain, long-term effects of psychological stress and effects of blood-brain-barrier (BBB) adaptation to dysglycemia on the generation of hyperglycemia are also taken into account in the model. RESULTS: It is shown that simulation profiles obtained from the model are qualitatively or partially quantitatively consistent with clinical data, concerning the GIG regulatory system responses to bolus glucose, stepwise and continuous glucose infusion. Simulations also revealed that both stress and BBB adaptation contribute to the generation of hyperglycemia. CONCLUSION: Simulations of the model of a healthy person under long-term severe stress demonstrated that feedback control of brain glucose concentration results in elevation of blood glucose level. In this paper, we try to suggest that hyperglycemia in diabetes may be a normal outcome of brain glucose homeostasis. BioMed Central 2009-11-27 /pmc/articles/PMC2801528/ /pubmed/19943948 http://dx.doi.org/10.1186/1742-4682-6-26 Text en Copyright ©2009 Gaohua and Kimura; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gaohua, Lu Kimura, Hidenori A mathematical model of brain glucose homeostasis |
title | A mathematical model of brain glucose homeostasis |
title_full | A mathematical model of brain glucose homeostasis |
title_fullStr | A mathematical model of brain glucose homeostasis |
title_full_unstemmed | A mathematical model of brain glucose homeostasis |
title_short | A mathematical model of brain glucose homeostasis |
title_sort | mathematical model of brain glucose homeostasis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801528/ https://www.ncbi.nlm.nih.gov/pubmed/19943948 http://dx.doi.org/10.1186/1742-4682-6-26 |
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