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Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis

BACKGROUND: In mammals, vasopressin (AVP) is released from magnocellular neurons of the hypothalamus when osmotic pressure exceeds a fixed set-point. AVP participates to the hydromineral homeostasis (HH) by controlling water excretion at the level of the kidneys. Our current understanding of the HH...

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Autores principales: Nadeau, Louis, Arbour, Danielle, Mouginot, Didier
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939538/
https://www.ncbi.nlm.nih.gov/pubmed/20738873
http://dx.doi.org/10.1186/1472-6793-10-17
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author Nadeau, Louis
Arbour, Danielle
Mouginot, Didier
author_facet Nadeau, Louis
Arbour, Danielle
Mouginot, Didier
author_sort Nadeau, Louis
collection PubMed
description BACKGROUND: In mammals, vasopressin (AVP) is released from magnocellular neurons of the hypothalamus when osmotic pressure exceeds a fixed set-point. AVP participates to the hydromineral homeostasis (HH) by controlling water excretion at the level of the kidneys. Our current understanding of the HH and AVP secretion is the result of a vast amount of data collected over the five past decades. This experimental data was collected using a number of systems under different conditions, giving a fragmented view of the components involved in HH. RESULTS: Here, we present a high-level model of the rat HH based on selected published results to predict short-term (hours) to long-term (days) variation of six major homeostatic parameters: (1) the extracellular sodium concentration, (2) the AVP concentration, (3) the intracellular volume, (4) the extracellular volume, (5) the urine volume and (6) the water intake. The simulation generates quantitative predictions like the daily mean of the extracellular sodium concentration (142.2 mmol/L), the AVP concentration, (1.7 pg/ml), the intracellular volume (45.3 ml/100 g body weight - bw), the extracellular volume (22.6 ml/100 g bw), the urine volume (11.8 ml/100 g bw) and the cumulative water intake (18 ml/100 g bw). The simulation also computes the dynamics of all these parameters with a high temporal resolution of one minute. This high resolution predicts the circadian fluctuation of the AVP secretion (5 ± 2 pg/ml) and defines the limits of a restoration and a maintenance phase in the HH (2.1 pg/ml). Moreover, the simulation can predict the action of pharmacological compounds that disrupt the HH. As an example, we tested the action of a diuretic (furosemide) combined with a sodium deficient diet to generate quantitative prediction on the extracellular sodium concentration (134 mmol/L) and the need-induced water intake (20.3 ml/100 g bw). These simulated data are compatible with experimental data (136 ± 3 mmol/L and 17.5 ± 3.5 ml/100 g bw, respectively). CONCLUSION: The quantitative agreement of the predictions with published experimental data indicates that our simplified model of the HH integrates most of the essential systems to predict realistic physiological values and dynamics under a set of normal and perturbed hydromineral conditions.
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spelling pubmed-29395382010-09-21 Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis Nadeau, Louis Arbour, Danielle Mouginot, Didier BMC Physiol Research Article BACKGROUND: In mammals, vasopressin (AVP) is released from magnocellular neurons of the hypothalamus when osmotic pressure exceeds a fixed set-point. AVP participates to the hydromineral homeostasis (HH) by controlling water excretion at the level of the kidneys. Our current understanding of the HH and AVP secretion is the result of a vast amount of data collected over the five past decades. This experimental data was collected using a number of systems under different conditions, giving a fragmented view of the components involved in HH. RESULTS: Here, we present a high-level model of the rat HH based on selected published results to predict short-term (hours) to long-term (days) variation of six major homeostatic parameters: (1) the extracellular sodium concentration, (2) the AVP concentration, (3) the intracellular volume, (4) the extracellular volume, (5) the urine volume and (6) the water intake. The simulation generates quantitative predictions like the daily mean of the extracellular sodium concentration (142.2 mmol/L), the AVP concentration, (1.7 pg/ml), the intracellular volume (45.3 ml/100 g body weight - bw), the extracellular volume (22.6 ml/100 g bw), the urine volume (11.8 ml/100 g bw) and the cumulative water intake (18 ml/100 g bw). The simulation also computes the dynamics of all these parameters with a high temporal resolution of one minute. This high resolution predicts the circadian fluctuation of the AVP secretion (5 ± 2 pg/ml) and defines the limits of a restoration and a maintenance phase in the HH (2.1 pg/ml). Moreover, the simulation can predict the action of pharmacological compounds that disrupt the HH. As an example, we tested the action of a diuretic (furosemide) combined with a sodium deficient diet to generate quantitative prediction on the extracellular sodium concentration (134 mmol/L) and the need-induced water intake (20.3 ml/100 g bw). These simulated data are compatible with experimental data (136 ± 3 mmol/L and 17.5 ± 3.5 ml/100 g bw, respectively). CONCLUSION: The quantitative agreement of the predictions with published experimental data indicates that our simplified model of the HH integrates most of the essential systems to predict realistic physiological values and dynamics under a set of normal and perturbed hydromineral conditions. BioMed Central 2010-08-25 /pmc/articles/PMC2939538/ /pubmed/20738873 http://dx.doi.org/10.1186/1472-6793-10-17 Text en Copyright ©2010 Nadeau et al; 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 Article
Nadeau, Louis
Arbour, Danielle
Mouginot, Didier
Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title_full Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title_fullStr Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title_full_unstemmed Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title_short Computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
title_sort computational simulation of vasopressin secretion using a rat model of the water and electrolyte homeostasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939538/
https://www.ncbi.nlm.nih.gov/pubmed/20738873
http://dx.doi.org/10.1186/1472-6793-10-17
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