Abstract

Dietary protein has been shown to increase iron (Fe) absorption by improving bioavailability. Little data are available on the effect of dietary protein on Fe transporter expression.As part of a study designed to evaluate the impact of dietary protein on mineral homeostasis, a whole genome microarray screen was performed using RNA prepared from duodenal intestinocytes of rats ingesting low (5%) or high (40%) casein diets for one week. Of 91 genes that were significantly up‐regulated in the 40% group, 3 were Fe transporters. DMT1 expression was 2.5‐fold greater in the 40% compared to the 5% group, while Cybrd1 and Tfrc were 1.6‐fold greater. Q‐PCR using the same RNA employed in the microarray screen confirmed these findings.When compared to the level of expression on a 20% diet (usual rat chow), DMT1 was 4‐fold higher in the 40% group (p<0.001), Cybrd1 was 2.2‐fold higher (p<0.05) while Tfrc was not different.To determine if the observed changes in expression of DMT1 and Cybrd1 were associated with changes in Fe homeostasis, a balance study was performed in rats ingesting 5, 20 and 40% protein diets. By the Kruskal‐Wallis test there was a significant effect of dietary protein on Fe balance and by post hoc analysis Fe absorption was greater in animals consuming the 40% vs. 5% diet (p<0.01).These data suggest that increasing dietary protein augments Fe absorption in part by inducing the expression of duodenal Fe transporters.Grant Funding Source: USDA

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.