Peripheral Administration of Tumor Necrosis Factor-Alpha Induces Neuroinflammation and Sickness but Not Depressive-Like Behavior in Mice

Biomed Res Int. 2015:2015:716920. doi: 10.1155/2015/716920. Epub 2015 Jul 28.

Abstract

Clinical observations indicate that activation of the TNF-α system may contribute to the development of inflammation-associated depression. Here, we tested the hypothesis that systemic upregulation of TNF-α induces neuroinflammation and behavioral changes relevant to depression. We report that a single intraperitoneal injection of TNF-α in mice increased serum and brain levels of the proinflammatory mediators TNF-α, IL-6, and MCP-1, in a dose- and time-dependent manner, but not IL-1β. Protein levels of the anti-inflammatory cytokine IL-10 increased in serum but not in the brain. The transient release of immune molecules was followed by glial cell activation as indicated by increased astrocyte activation in bioluminescent Gfap-luc mice and elevated immunoreactivity against the microglial marker Iba1 in the dentate gyrus of TNF-α-challenged mice. Additionally, TNF-α-injected mice were evaluated in a panel of behavioral tests commonly used to study sickness and depressive-like behavior in rodents. Our behavioral data imply that systemic administration of TNF-α induces a strong sickness response characterized by reduced locomotor activity, decreased fluid intake, and body weight loss. Depressive-like behavior could not be separated from sickness at any of the time points studied. Together, these results demonstrate that peripheral TNF-α affects the central nervous system at a neuroimmune and behavioral level.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects*
  • Biomarkers / metabolism
  • Brain / metabolism*
  • Brain / pathology
  • Calcium-Binding Proteins / metabolism
  • Chemokine CCL2 / metabolism
  • Depression / metabolism
  • Depression / pathology
  • Encephalitis / chemically induced
  • Encephalitis / metabolism*
  • Encephalitis / pathology
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Inflammation / pathology
  • Interleukin-10 / metabolism
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Microfilament Proteins / metabolism
  • Tumor Necrosis Factor-alpha / adverse effects*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Aif1 protein, mouse
  • Biomarkers
  • Calcium-Binding Proteins
  • Ccl2 protein, mouse
  • Chemokine CCL2
  • IL10 protein, mouse
  • IL1B protein, mouse
  • Interleukin-1beta
  • Interleukin-6
  • Microfilament Proteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-10