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Opportunities for plant-derived enhancers for iron, zinc, and calcium bioavailability: A review

Journal

Publisher

WILEY
DOI: 10.1111/1541-4337.12669

Keywords

mineral bioaccessibility; bioavailability enhancers; pulse protein; digestive tract; functional foods

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Understanding the mechanisms of interactions between dietary elements, their salts, and complexing/binding ligands is crucial for managing deficiency and toxicity. Despite some research on plant macro/micronutrients as bioavailability enhancing ligands, the understanding of their role in improving element bioavailability is still limited. Further research is needed to elucidate the binding behavior of potential ligands in the human diet and validate their effects using pharmacokinetic approaches and GI models.
Understanding of the mechanism of interactions between dietary elements, their salts, and complexing/binding ligands is vital to manage both deficiency and toxicity associated with essential element bioavailability. Numerous mineral ligands are found in both animal and plant foods and are known to exert bioactivity via element chelation resulting in modulation of antioxidant capacity or micobiome metabolism among other physiological outcomes. However, little is explored in the context of dietary mineral ligands and element bioavailability enhancement, particularly with respect to ligands from plant-derived food sources. This review highlights a novel perspective to consider various plant macro/micronutrients as prospective bioavailability enhancing ligands of three essential elements (Fe, Zn, and Ca). We also delineate the molecular mechanisms of the ligand-binding interactions underlying mineral bioaccessibility at the luminal level. We conclude that despite current understandings of some of the structure-activity relationships associated with strong mineral-ligand binding, the physiological links between ligands as element carriers and uptake at targeted sites throughout the gastrointestinal (GI) tract still require more research. The binding behavior of potential ligands in the human diet should be further elucidated and validated using pharmacokinetic approaches and GI models.

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