Systemic immune activation leads to neuroinflammation and sickness behavior in mice

Mediators Inflamm. 2013:2013:271359. doi: 10.1155/2013/271359. Epub 2013 Jul 10.

Abstract

Substantial evidence indicates an association between clinical depression and altered immune function. Systemic administration of bacterial lipopolysaccharide (LPS) is commonly used to study inflammation-associated behavioral changes in rodents. In these experiments, we tested the hypothesis that peripheral immune activation leads to neuroinflammation and depressive-like behavior in mice. We report that systemic administration of LPS induced astrocyte activation in transgenic GFAP-luc mice and increased immunoreactivity against the microglial marker ionized calcium-binding adapter molecule 1 in the dentate gyrus of wild-type mice. Furthermore, LPS treatment caused a strong but transient increase in cytokine levels in the serum and brain. In addition to studying LPS-induced neuroinflammation, we tested whether sickness could be separated from depressive-like behavior by evaluating LPS-treated mice in a panel of behavioral paradigms. Our behavioral data indicate that systemic LPS administration caused sickness and mild depressive-like behavior. However, due to the overlapping time course and mild effects on depression-related behavior per se, it was not possible to separate sickness from depressive-like behavior in the present rodent model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology*
  • Behavior, Animal
  • Brain / immunology
  • Brain / metabolism
  • Calcium-Binding Proteins / metabolism
  • Choice Behavior
  • Cytokines / blood
  • Cytokines / metabolism
  • Depression / immunology*
  • Disease Models, Animal
  • Feeding Behavior
  • Illness Behavior*
  • Immunohistochemistry
  • Inflammation / pathology*
  • Lipopolysaccharides / chemistry
  • Luminescence
  • Male
  • Mice
  • Mice, Transgenic
  • Microfilament Proteins / metabolism
  • Microglia / metabolism
  • Neurons / metabolism
  • Sucrose / chemistry

Substances

  • Aif1 protein, mouse
  • Calcium-Binding Proteins
  • Cytokines
  • Lipopolysaccharides
  • Microfilament Proteins
  • Sucrose