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Biology subjects

Dowrick, J. M.

Publications and source records attributed to Dowrick, J. M..

2 recordsLinked to original sources

The biophysical basis of enterocyte homeostasis

We present an approach to analysing cell homeostasis using a bond graph modelling approach that ensures that the conservation laws of physics (conservation of mass, charge, and energy, respectively) are satisfied for the interdependent biochemical, electrical, mechanical, and thermal energy storage mechanisms operating within the cell. We apply the bond graph approach to several cell membrane transport mechanisms and then consider how physics constrains intracellular electrolyte homeostasis for enterocytes (the epithelial absorptive cells of the gut). The model includes the electrogenic sodium-potassium ATPase pump (NKA), the glucose transporter (GLUT2), and an inwardly rectifying potassium channel, all in the basolateral membrane, and the electrogenic sodium-driven glucose transporter (SGLT1) in the apical membrane. Glycolysis converts the imported glucose to ATP to drive NKA. For specified levels of sodium, potassium, and glucose in the blood, the model demonstrates how enterocytes absorb sodium and glucose from the gut and transfer glucose to the blood while maintaining the membrane potential and homeostasis of intracellular sodium and potassium. The Gibbs free energy available from the ATP hydrolysis ensures that the cell operates as a sodium battery with a high external to internal ratio of sodium concentration in order to provide the energy for many other cellular transport processes. We show that the 3:2 stoichiometry of Na+/K+ exchange in NKA, coupled with 2:1 Na+/glucose cotransport in SGLT1, a 1:2:2 ratio between glucose consumption and ATP and water production in glycolysis, and K+ and glucose efflux through Kir and GLUT2, respectively, provides a balanced system that maintains homeostasis of intracellular Na+, K+, glucose, ATP and water, and homeostasis of the membrane potential, under varying levels of transport of glucose from the gut to the blood. We also show how the flux expressions for SLC transporters, ATPase pumps and ion channels can all be expressed in a consistent and thermodynamically valid way.

bioengineering↗

A case for slow-wave morphology as a functional biomarker of gastric disease

AimUnderlying bioelectrical slow waves are critical for regulating gastric motility, and abnormal spatiotemporal slow-wave dysrhythmias are associated with a range of gastrointestinal disorders. However, the definition and role of the morphology of gastric slow-wave signals have remained limited. This study aimed to investigate the potential of gastric slow-wave morphology as an actionable biomarker. MethodsData were repurposed from a study where, following ethical approval, a control cohort (n=9) and a pathological cohort of patients with chronic unexplained nausea and vomiting (CUNV; n=8) underwent intra-operative high-resolution serosal electrical mapping (96-256 electrodes, 4.0-5.2 mm spacing). Slow waves were identified using validated software, and spatiotemporally averaged waveforms were compared between cohorts. These waveforms were replicated in a computational model of gastric slow-wave propagation to explore potential functional implications. ResultsThe slow-wave morphology of the CUNV cohort exhibited a more gradual recovery stroke compared to controls, which manifested as an increase in the normalized recovery stroke area [0.206 (95% CI: 0.169-0.247) vs. 0.134 (95% CI: 0.106-0.166); p=0.011]. Computational modeling showed that these morphological differences could drive spatial slow-wave dysrhythmias. Considering the evident functional importance of gastric slow-wave morphology, we highlighted the three typical morphological features: 1) rapid, brief upstroke, 2) downstroke, and 3) biphasic recovery stroke. ConclusionAltogether, this study presents a case for gastric slow-wave morphology as a biomarker of gastric health and disease and lays a foundation for the standardization of future slow-wave morphology research. PRACTITIONER POINTSO_LIAbnormal spatial slow-wave propagation is associated with a range of gastrointestinal motility disorders, but morphology has had limited consideration. C_LIO_LISlow-wave morphology differs between cohorts of healthy controls and patients with chronic unexplained nausea and vomiting. C_LIO_LIMultiscale mathematical modeling indicates that a disruption to the slow-wave recovery stroke may contribute to spatial disorganization. C_LI

physiology↗