Circulating Human Hepcidin-25 Concentrations Display a Diurnal Rhythm, Increase with Prolonged Fasting, and Are Reduced by Growth Hormone Administration

Author:

Troutt Jason S1,Rudling Mats234,Persson Lena234,Ståhle Lars5,Angelin Bo234,Butterfield Anthony M1,Schade Andrew E1,Cao Guoqing1,Konrad Robert J1

Affiliation:

1. Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN

2. Metabolism Unit, Department of Endocrinology, Metabolism and Diabetes, and

3. Department of Medicine, Karolinska Institute at Karolinska University Hospital at Huddinge, Stockholm, Sweden

4. Molecular Nutrition Unit, Department of Bioscience and Nutrition, and

5. Department of Clinical Pharmacology, Karolinska Institute at Karolinska University Hospital at Huddinge, Stockholm, Sweden

Abstract

Abstract BACKGROUND Hepcidin-25 reduces iron absorption by binding to the intestinal iron transporter ferroportin and causing its degradation. Currently, little is known about the basal regulation of circulating hepcidin-25. In addition, although erythropoietin administration has been reported to decrease the circulating hepcidin concentration, information is limited regarding how other stimulators of erythropoiesis, such as growth hormone (GH), might alter hepcidin-25 concentrations. METHODS We used a sensitive and specific hepcidin-25 dual–monoclonal antibody sandwich immunoassay to measure hepcidin-25 in healthy human volunteers at various time points throughout the day and during 3 days of fasting and subsequent refeeding. We also measured hepcidin-25 concentrations in healthy volunteers after GH administration. RESULTS In healthy individuals, hepcidin-25 concentrations displayed a diurnal variation, with concentrations being lowest in the early morning and steadily increasing throughout the day before declining during the evening hours, a pattern that was not influenced by food intake. Prolonged fasting produced statistically significant increases in hepcidin-25 concentrations. Refeeding reversed this process, and GH administration markedly decreased hepcidin-25 concentrations. CONCLUSIONS Our results indicate that in humans, hepcidin-25 exhibits diurnal changes that can be altered by prolonged fasting, which increases hepcidin-25 concentrations approximately 3-fold after 3 days of fasting, possibly owing to a suppression of erythropoiesis that may occur during the fasting state to preserve tissue iron concentrations. In contrast, GH administration decreased hepcidin-25 concentrations by approximately 65%, presumably by stimulating erythropoiesis. These results indicate that circulating hepcidin-25 concentrations display much more dynamic and rapid variation than might have been anticipated previously.

Funder

Eli Lilly and Company

Vetenskapsrådet

Stockholm City Council

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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