The chelation of colonic luminal iron by a unique sodium alginate for the improvement of gastrointestinal health
Research output: Contribution to journal › Article › peer-review
Colleges, School and Institutes
SCOPE: Scope: Iron is an essential nutrient. However, in animal models, excess unabsorbed dietary iron residing within the colonic lumen has been shown to exacerbate inflammatory bowel disease and intestinal cancer. Therefore the aims of this study were to screen a panel of alginates to identify a therapeutic that can chelate this pool of iron and thus be beneficial for intestinal health.
SCOPE: Methods and results: Using several in vitro intestinal models it is evident that only one alginate (Manucol LD) of the panel tested was able to inhibit intracellular iron accumulation as assessed by iron mediated ferritin induction, transferrin receptor expression, intracellular (59) Fe concentrations and by measuring iron flux across a Caco-2 monolayer. Additionally, Manucol LD suppressed iron absorption in mice which was associated with increased faecal iron levels indicating iron chelation within the gastrointestinal tract. Furthermore, the bioactivity of Manucol LD was found to be highly dependent on both its molecular weight and its unique compositional sequence.
SCOPE: Conclusion: Manucol LD could be useful for the chelation of this detrimental pool of unabsorbed iron and it could be fortified in foods to enhance intestinal health. This article is protected by copyright. All rights reserved.
|Journal||Molecular Nutrition & Food Research|
|Early online date||2 May 2016|
|Publication status||E-pub ahead of print - 2 May 2016|