Intestinal transport characteristics and metabolism of C-glucosyl dihydrochalcone, aspalathin
Date
2017
Journal Title
Journal ISSN
Volume Title
Publisher
MDPI
Abstract
Insight into the mechanisms of intestinal transport and metabolism of aspalathin will provide important information for dose optimisation, in particular for studies using mouse models. Aspalathin transportation across the intestinal barrier (Caco-2 monolayer) tested at 1–150 µM had an apparent rate of permeability (Papp) typical of poorly absorbed compounds (1.73 × 10⁻⁶cm/s). Major glucose transporters, sodium glucose linked transporter 1 (SGLT1) and glucose transporter 2 (GLUT2), and efflux protein (P-glycoprotein, PgP) (1.84 × 10⁻⁶ cm/s; efflux ratio: 1.1) were excluded as primary transporters, since the Papp of aspalathin was not affected by the presence of specific inhibitors. The Papp of aspalathin was also not affected by constituents of aspalathin-enriched rooibos extracts, but was affected by high glucose concentration (20.5 mM), which decreased the Papp value to 2.9 × 10⁻⁷ cm/s. Aspalathin metabolites (sulphated, glucuronidated and methylated) were found in mouse urine, but not in blood, following an oral dose of 50 mg/kg body weight of the pure compound. Sulphates were the predominant metabolites. These findings suggest that aspalathin is absorbed and metabolised in mice to mostly sulphate conjugates detected in urine. Mechanistically, we showed that aspalathin is not actively transported by the glucose transporters, but presumably passes the monolayer paracellularly.
Description
CITATION: Bowles, S., et al. 2017. Intestinal transport characteristics and metabolism of C-glucosyl dihydrochalcone, aspalathin. Molecules, 22(4):554, doi:10.3390/molecules22040554.
The original publication is available at https://www.mdpi.com
The original publication is available at https://www.mdpi.com
Keywords
Bioavailability, Metabolism, Aspalathin
Citation
Bowles, S., et al. 2017. Intestinal transport characteristics and metabolism of C-glucosyl dihydrochalcone, aspalathin. Molecules, 22(4):554, doi:10.3390/molecules22040554