Mild to Moderate Food Deprivation Increases Hepcidin and Results in Hypoferremia and Tissue Iron Sequestration in Mice
Short-term starvation and severe food deprivation (FD) reduce dietary iron absorption and restricts iron to tissues, thereby limiting the amount of iron available for erythropoiesis. These effects may be mediated by increases in the iron regulatory hormone hepcidin; however, whether mild to moderate...
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Published in: | The Journal of nutrition Vol. 152; no. 10; p. 2198 |
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01-10-2022
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Abstract | Short-term starvation and severe food deprivation (FD) reduce dietary iron absorption and restricts iron to tissues, thereby limiting the amount of iron available for erythropoiesis. These effects may be mediated by increases in the iron regulatory hormone hepcidin; however, whether mild to moderate FD has similar effects on hepcidin and iron homeostasis is not known.
To determine the effects of varying magnitudes and durations of FD on hepcidin and indicators of iron status in male and female mice.
Male and female C57BL/6J mice (14 wk old; n = 170) were randomly assigned to consume AIN-93M diets ad libitum (AL) or varying magnitudes of FD (10%, 20%, 40%, 60%, 80%, or 100%). FD was based on the average amount of food consumed by the AL males or females, and food was split into morning and evening meals. Mice were euthanized at 48 h and 1, 2, and 3 wk, and hepcidin and indicators of iron status were measured. Data were analyzed by Pearson correlation and one-way ANOVA.
Liver hepcidin mRNA was positively correlated with the magnitude of FD at all time points (P < 0.05). At 3 wk, liver hepcidin mRNA increased 3-fold with 10% and 20% FD compared with AL and was positively associated with serum hepcidin (R = 0.627, P < 0.0001). Serum iron was reduced by ∼65% (P ≤ 0.01), and liver nonheme iron concentrations were ∼75% greater (P ≤ 0.01) with 10% and 20% FD for 3 wk compared with AL. Liver hepcidin mRNA at 3 wk was positively correlated with liver Bmp6 (R = 0.765, P < 0.0001) and liver gluconeogenic enzymes (R = >0.667, P < 0.05) but not markers of inflammation (P > 0.05).
FD increases hepcidin in male and female mice and results in hypoferremia and tissue iron sequestration. These findings suggest that increased hepcidin with FD may contribute to the disturbances in iron homeostasis with undernutrition. |
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AbstractList | Short-term starvation and severe food deprivation (FD) reduce dietary iron absorption and restricts iron to tissues, thereby limiting the amount of iron available for erythropoiesis. These effects may be mediated by increases in the iron regulatory hormone hepcidin; however, whether mild to moderate FD has similar effects on hepcidin and iron homeostasis is not known.
To determine the effects of varying magnitudes and durations of FD on hepcidin and indicators of iron status in male and female mice.
Male and female C57BL/6J mice (14 wk old; n = 170) were randomly assigned to consume AIN-93M diets ad libitum (AL) or varying magnitudes of FD (10%, 20%, 40%, 60%, 80%, or 100%). FD was based on the average amount of food consumed by the AL males or females, and food was split into morning and evening meals. Mice were euthanized at 48 h and 1, 2, and 3 wk, and hepcidin and indicators of iron status were measured. Data were analyzed by Pearson correlation and one-way ANOVA.
Liver hepcidin mRNA was positively correlated with the magnitude of FD at all time points (P < 0.05). At 3 wk, liver hepcidin mRNA increased 3-fold with 10% and 20% FD compared with AL and was positively associated with serum hepcidin (R = 0.627, P < 0.0001). Serum iron was reduced by ∼65% (P ≤ 0.01), and liver nonheme iron concentrations were ∼75% greater (P ≤ 0.01) with 10% and 20% FD for 3 wk compared with AL. Liver hepcidin mRNA at 3 wk was positively correlated with liver Bmp6 (R = 0.765, P < 0.0001) and liver gluconeogenic enzymes (R = >0.667, P < 0.05) but not markers of inflammation (P > 0.05).
FD increases hepcidin in male and female mice and results in hypoferremia and tissue iron sequestration. These findings suggest that increased hepcidin with FD may contribute to the disturbances in iron homeostasis with undernutrition. |
Author | Barney, Jr, David E Margolis, Lee M Murphy, Robert D Murphy, Nancy E Hennigar, Stephen R James, Kelsey M Ippolito, James R Miller, Katelyn M Gwin, Jess A McClung, James P Pasiakos, Stefan M |
Author_xml | – sequence: 1 givenname: Robert D surname: Murphy fullname: Murphy, Robert D organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA – sequence: 2 givenname: Kelsey M surname: James fullname: James, Kelsey M organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA – sequence: 3 givenname: James R surname: Ippolito fullname: Ippolito, James R organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA – sequence: 4 givenname: David E surname: Barney, Jr fullname: Barney, Jr, David E organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA – sequence: 5 givenname: Katelyn M surname: Miller fullname: Miller, Katelyn M organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA – sequence: 6 givenname: Nancy E surname: Murphy fullname: Murphy, Nancy E organization: Military Nutrition Division, US Army Research Institute of Environmental Medicine, Natick, MA, USA – sequence: 7 givenname: Jess A surname: Gwin fullname: Gwin, Jess A organization: Military Nutrition Division, US Army Research Institute of Environmental Medicine, Natick, MA, USA – sequence: 8 givenname: Stefan M surname: Pasiakos fullname: Pasiakos, Stefan M organization: Military Performance Division, US Army Research Institute of Environmental Medicine, Natick, MA, USA – sequence: 9 givenname: James P surname: McClung fullname: McClung, James P organization: Military Nutrition Division, US Army Research Institute of Environmental Medicine, Natick, MA, USA – sequence: 10 givenname: Lee M surname: Margolis fullname: Margolis, Lee M organization: Military Nutrition Division, US Army Research Institute of Environmental Medicine, Natick, MA, USA – sequence: 11 givenname: Stephen R surname: Hennigar fullname: Hennigar, Stephen R email: stephen.hennigar@pbrc.edu organization: Department of Nutrition and Integrative Physiology, Florida State University, Tallahassee, FL, USA; Pennington Biomedical Research Center, Baton Rouge, LA, USA. Electronic address: stephen.hennigar@pbrc.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36774177$$D View this record in MEDLINE/PubMed |
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Keywords | malnutrition undernutrition energy balance gluconeogenesis iron status |
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SubjectTerms | Animals Female Food Deprivation Hepcidins - genetics Iron Male Mice Mice, Inbred C57BL RNA, Messenger |
Title | Mild to Moderate Food Deprivation Increases Hepcidin and Results in Hypoferremia and Tissue Iron Sequestration in Mice |
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