A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products

There are no known physiological-based digestion models that depict glucoraphanin (GR) to sulforaphane (SR) conversion and subsequent absorption. The aim of this research was to make a physiological-based digestion model that includes SR formation, both by endogenous myrosinase and gut bacterial enz...

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Autores principales: Quchat Shekarri, Matthijs Dekker
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/b88533f3681c4f8b886f938e6a0d8a05
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spelling oai:doaj.org-article:b88533f3681c4f8b886f938e6a0d8a052021-11-25T17:35:19ZA Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products10.3390/foods101127612304-8158https://doaj.org/article/b88533f3681c4f8b886f938e6a0d8a052021-11-01T00:00:00Zhttps://www.mdpi.com/2304-8158/10/11/2761https://doaj.org/toc/2304-8158There are no known physiological-based digestion models that depict glucoraphanin (GR) to sulforaphane (SR) conversion and subsequent absorption. The aim of this research was to make a physiological-based digestion model that includes SR formation, both by endogenous myrosinase and gut bacterial enzymes, and to simulate the SR bioavailability. An 18-compartment model (mouth, two stomach, seven small intestine, seven large intestine, and blood compartments) describing transit, reactions and absorption was made. The model, consisting of differential equations, was fit to data from a human intervention study using Mathwork’s Simulink and Matlab software. SR urine metabolite data from participants who consumed different broccoli products were used to estimate several model parameters and validate the model. The products had high, medium, low, and zero myrosinase content. The model’s predicted values fit the experimental values very well. Parity plots showed that the predicted values closely matched experimental values for the high (<i>r</i><sup>2</sup> = 0.95), and low (<i>r</i><sup>2</sup> = 0.93) products, but less so for the medium (<i>r</i><sup>2</sup> = 0.85) and zero (<i>r</i><sup>2</sup> = 0.78) myrosinase products. This is the first physiological-based model to depict the unique bioconversion processes of bioactive SR from broccoli. This model represents a preliminary step in creating a predictive model for the biological effect of SR, which can be used in the growing field of personalized nutrition.Quchat ShekarriMatthijs DekkerMDPI AGarticlephysiological-based modelsulforaphaneglucoraphanincompartmental modelbroccolibioavailabilityChemical technologyTP1-1185ENFoods, Vol 10, Iss 2761, p 2761 (2021)
institution DOAJ
collection DOAJ
language EN
topic physiological-based model
sulforaphane
glucoraphanin
compartmental model
broccoli
bioavailability
Chemical technology
TP1-1185
spellingShingle physiological-based model
sulforaphane
glucoraphanin
compartmental model
broccoli
bioavailability
Chemical technology
TP1-1185
Quchat Shekarri
Matthijs Dekker
A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
description There are no known physiological-based digestion models that depict glucoraphanin (GR) to sulforaphane (SR) conversion and subsequent absorption. The aim of this research was to make a physiological-based digestion model that includes SR formation, both by endogenous myrosinase and gut bacterial enzymes, and to simulate the SR bioavailability. An 18-compartment model (mouth, two stomach, seven small intestine, seven large intestine, and blood compartments) describing transit, reactions and absorption was made. The model, consisting of differential equations, was fit to data from a human intervention study using Mathwork’s Simulink and Matlab software. SR urine metabolite data from participants who consumed different broccoli products were used to estimate several model parameters and validate the model. The products had high, medium, low, and zero myrosinase content. The model’s predicted values fit the experimental values very well. Parity plots showed that the predicted values closely matched experimental values for the high (<i>r</i><sup>2</sup> = 0.95), and low (<i>r</i><sup>2</sup> = 0.93) products, but less so for the medium (<i>r</i><sup>2</sup> = 0.85) and zero (<i>r</i><sup>2</sup> = 0.78) myrosinase products. This is the first physiological-based model to depict the unique bioconversion processes of bioactive SR from broccoli. This model represents a preliminary step in creating a predictive model for the biological effect of SR, which can be used in the growing field of personalized nutrition.
format article
author Quchat Shekarri
Matthijs Dekker
author_facet Quchat Shekarri
Matthijs Dekker
author_sort Quchat Shekarri
title A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
title_short A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
title_full A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
title_fullStr A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
title_full_unstemmed A Physiological-Based Model for Simulating the Bioavailability and Kinetics of Sulforaphane from Broccoli Products
title_sort physiological-based model for simulating the bioavailability and kinetics of sulforaphane from broccoli products
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/b88533f3681c4f8b886f938e6a0d8a05
work_keys_str_mv AT quchatshekarri aphysiologicalbasedmodelforsimulatingthebioavailabilityandkineticsofsulforaphanefrombroccoliproducts
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AT matthijsdekker physiologicalbasedmodelforsimulatingthebioavailabilityandkineticsofsulforaphanefrombroccoliproducts
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