The Development of Lentil Derived Protein-Iron Complexes and Their Effects on Iron Deficiency Anemia in Vitro
Loading...
Date
Authors
Evcan, Ezgi
Güleç, Şükrü
Journal Title
Journal ISSN
Volume Title
Publisher
Open Access Color
Green Open Access
No
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
Iron deficiency anemia (IDA) is the most common nutrient-dependent health problem in the world and could be reversed by commercially available iron supplementation. The form of iron supplement is important due to its toxicity on the gastrointestinal system (GI), so the development of new dietary strategies might be important for the prevention of IDA. It has been shown that plant-based proteins bind to iron and might decrease the free form of iron before absorption and increase iron bioavailability. Thus, we aimed to form lentil derived protein-iron complexes and to test the functional properties of hydrolysed protein-iron complexes in anemic Caco-2 cell line. Our main findings were that (i) lentil derived proteins had the capacity to chelate iron minerals and (ii) hydrolysed protein-iron complexes significantly reduced the mRNA levels of iron regulated divalent metal transporter-1 (DMT1), transferrin receptor (TFR), and ankyrin repeat domain 37 (ANKRD37) marker genes that were induced by iron deficiency anemia. The current findings suggest that hydrolysed protein-iron complexes might have functional properties in iron deficiency anemia in vitro. Further in vivo studies are necessary to show lentil derived proteins and iron might be used as supplements or food additives to reduce the risk of iron deficiency anemia.
Description
Keywords
Iron deficiency anemia, Plant proteins, Iron compounds, Anemia, Iron-Deficiency, Iron, Humans, Lens Plant, Caco-2 Cells, Hydrogen-Ion Concentration, Plant Proteins
Fields of Science
0301 basic medicine, 0303 health sciences, 03 medical and health sciences
Citation
WoS Q
Scopus Q

OpenCitations Citation Count
16
Source
Volume
11
Issue
5
Start Page
4185
End Page
4192
PlumX Metrics
Citations
CrossRef : 15
Scopus : 20
PubMed : 7
Captures
Mendeley Readers : 40
Google Scholar™


