Diurnal variations in iron concentrations and expression of genes involved in iron absorption and metabolism in pigs

Biochem Biophys Res Commun. 2017 Sep 2;490(4):1210-1214. doi: 10.1016/j.bbrc.2017.06.187. Epub 2017 Jul 1.

Abstract

Diurnal variations in serum iron levels have been well documented in clinical studies, and serum iron is an important diagnostic index for iron-deficiency anemia. However, the underlying mechanism of dynamic iron regulation in response to the circadian rhythm is still unclear. In this study, we investigated daily variations in iron status in the plasma and liver of pigs. The transcripts encoding key factors involved in iron uptake and homeostasis were evaluated. The results showed that iron levels in the plasma and liver exhibited diurnal rhythms. Diurnal variations were also observed in transcript levels of divalent metal transporter 1 (DMT1), membrane-associated ferric reductase 1 (DCYTB), and transferrin receptor (TfR) in the duodenum and jejunum, as well as hepcidin (HAMP) and TfR in the liver. Moreover, the results showed a network in which diurnal variations in systemic iron levels were tightly regulated by hepcidin and Tf/TfR via DCYTB and DMT1. These findings provide new insights into circadian iron homeostasis regulation. The diurnal variations in serum iron levels may also have pathophysiological implications for clinical diagnostics related to iron deficiency anemia in pigs.

Keywords: Diurnal variation; Homeostasis; Iron; Pig; Up take.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cation Transport Proteins / genetics*
  • Cation Transport Proteins / metabolism
  • Circadian Rhythm / physiology*
  • FMN Reductase / genetics*
  • FMN Reductase / metabolism
  • Iron / blood*
  • Iron / metabolism*
  • Liver / chemistry
  • Liver / metabolism
  • Receptors, Transferrin / genetics*
  • Receptors, Transferrin / metabolism
  • Swine

Substances

  • Cation Transport Proteins
  • Receptors, Transferrin
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Iron
  • FMN Reductase
  • ferric citrate iron reductase