Impaired recovery from peritoneal inflammation in a mouse model of mild dietary zinc restriction

Mol Nutr Food Res. 2016 Mar;60(3):672-81. doi: 10.1002/mnfr.201500688. Epub 2016 Feb 2.

Abstract

Scope: Mild dietary zinc (Zn) deficiency is wide-spread in human populations, but the effect on Zn-dependent processes of immune function and healing are not well understood. The consequences of mild dietary Zn restriction were examined in two mouse models of inflammation and recovery.

Methods and results: Male C57BL/6 mice were fed a Zn adequate diet (ZA, 30 mg Zn/kg diet), or diets containing sub-optimal Zn levels (ZM, 15 mg Zn/kg diet; ZD, 10 mg Zn/kg diet) for 30 days before a thioglycollate peritonitis challenge. Plasma lipid profiles were distinct, with greater Zn restriction resulting in a greater impact on metabolites. The milder ZM diet was selected for immune studies. Peritoneal macrophages from ZM mice displayed increased phagocytosis and amplified pro-inflammatory cytokine (IL-1β, IL-6, and TNFα) release compared to ZA, at baseline and after a secondary LPS challenge. Splenocytes isolated from ZM mice displayed an increase in IL-6 and a reduction in anti-inflammatory IL-4 compared to ZA. Cytokine levels in plasma were unaltered. Following mechanical manipulation of the intestines to induce ileus, ZM mice had delayed intestinal transit compared to ZA.

Conclusion: Mild Zn deficiency enhances local inflammatory responses, amplifying macrophage functions and delaying recovery from acute insults within the peritoneum.

Keywords: Ileus; Inflammation; Macrophage; Peritonitis; Zinc deficiency.

MeSH terms

  • Animals
  • Arachidonic Acid / metabolism
  • Cytokines / metabolism
  • Disease Models, Animal
  • Lipids / blood
  • Lysophosphatidylcholines / blood
  • Macrophages, Peritoneal / immunology
  • Macrophages, Peritoneal / physiology*
  • Male
  • Mice, Inbred C57BL
  • Peritonitis / etiology*
  • Phagocytosis / physiology
  • Zinc / deficiency*
  • Zinc / metabolism
  • Zinc / pharmacology

Substances

  • Cytokines
  • Lipids
  • Lysophosphatidylcholines
  • Arachidonic Acid
  • Zinc