S. J. Franks
Modelling the role of enzymatic pathways in the metabolism of docosahexaenoic acid by monocytes and its association with osteoarthritic pain
Franks, S. J.; Gowler, P. R.W.; Dunster, J. L.; Turnbull, J.; Gohir, S. A.; Kelly, A.; Valdes, A. M.; King, J. R.; Barrett, D. A.; Chapman, V.; Preston, S.
Authors
P. R.W. Gowler
J. L. Dunster
Dr James Turnbull JAMES.TURNBULL@NOTTINGHAM.AC.UK
RESEARCH FELLOW
S. A. Gohir
A. Kelly
Professor ANA VALDES Ana.Valdes@nottingham.ac.uk
PROFESSOR OF MOLECULAR & GENETIC EPIDEMIOLOGY
Professor JOHN KING JOHN.KING@NOTTINGHAM.AC.UK
PROFESSOR OF THEORETICAL MECHANICS
D. A. Barrett
Professor VICTORIA CHAPMAN VICTORIA.CHAPMAN@NOTTINGHAM.AC.UK
PROFESSOR OF NEUROPHARMACOLOGY
Professor SIMON PRESTON simon.preston@nottingham.ac.uk
PROFESSOR OF STATISTICS AND APPLIED MATHEMATICS
Abstract
Chronic pain is a major cause of disability and suffering in osteoarthritis (OA) patients. Endogenous specialised pro-resolving molecules (SPMs) curtail pro-inflammatory responses. One of the SPM intermediate oxylipins, 17-hydroxydocasahexaenoic acid (17-HDHA, a metabolite of docosahexaenoic acid (DHA)), is significantly associated with OA pain. The aim of this multidisciplinary work is to develop a mathematical model to describe the contributions of enzymatic pathways (and the genes that encode them) to the metabolism of DHA by monocytes and to the levels of the down-stream metabolites, 17-HDHA and 14-hydroxydocasahexaenoic acid (14-HDHA), motivated by novel clinical data from a study involving 30 participants with OA. The data include measurements of oxylipin levels, mRNA levels, measures of OA severity and self-reported pain scores. We propose a system of ordinary differential equations to characterise associations between the different datasets, in order to determine the homeostatic concentrations of DHA, 17-HDHA and 14-HDHA, dependent upon the gene expression of the associated metabolic enzymes. Using parameter-fitting methods, local sensitivity and uncertainty analysis, the model is shown to fit well qualitatively to experimental data. The model suggests that up-regulation of some ALOX genes may lead to the down-regulation of 17-HDHA and that dosing with 17-HDHA increases the production of resolvins, which helps to down-regulate the inflammatory response. More generally, we explore the challenges and limitations of modelling real data, in particular individual variability, and also discuss the value of gathering additional experimental data motivated by the modelling insights.
Citation
Franks, S. J., Gowler, P. R., Dunster, J. L., Turnbull, J., Gohir, S. A., Kelly, A., Valdes, A. M., King, J. R., Barrett, D. A., Chapman, V., & Preston, S. (2024). Modelling the role of enzymatic pathways in the metabolism of docosahexaenoic acid by monocytes and its association with osteoarthritic pain. Mathematical Biosciences, 374, Article 109228. https://doi.org/10.1016/j.mbs.2024.109228
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 3, 2024 |
Online Publication Date | Jun 6, 2024 |
Publication Date | 2024-08 |
Deposit Date | Jun 7, 2024 |
Publicly Available Date | Jun 7, 2025 |
Journal | Mathematical Biosciences |
Print ISSN | 0025-5564 |
Electronic ISSN | 1879-3134 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 374 |
Article Number | 109228 |
DOI | https://doi.org/10.1016/j.mbs.2024.109228 |
Keywords | Docosahexaenoic acid; Metabolites; Osteoarthritis; Gene expression; Mathematical model |
Public URL | https://nottingham-repository.worktribe.com/output/35733525 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0025556424000889?via%3Dihub |
Additional Information | This article is maintained by: Elsevier; Article Title: Modelling the role of enzymatic pathways in the metabolism of docosahexaenoic acid by monocytes and its association with osteoarthritic pain; Journal Title: Mathematical Biosciences; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.mbs.2024.109228; Content Type: article; Copyright: © 2024 The Author(s). Published by Elsevier Inc. |
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