Over-expression of TSPO in the hippocampal CA1 area alleviates cognitive dysfunction caused by lipopolysaccharide in mice

Brain Res. 2016 Sep 1:1646:402-409. doi: 10.1016/j.brainres.2016.06.001. Epub 2016 Jun 2.

Abstract

The translocator protein 18kDa (TSPO) is closely related to regulation of immune/inflammatory response. However, the putative role and signaling mechanisms of TSPO in regulation of neuroinflammation remain unclear. GV287 lentiviral vectors mediating TSPO over-expression were injected into bilateral hippocampal CA1 areas to test whether TSPO over-expression was neuroprotective in lipopolysaccharide (LPS)-induced mice model. Finasteride, a blocker of allopregnanolone production, was used to test whether the protective effects were related to steroideogenesis. The results demonstrated that TSPO over-expression increased progesterone and allopregnanolone synthesis. TSPO over-expression in CA1 area improved LPS-induced cognitive deficiency in mice and this cognitive improvement was reversed by finasteride administration. These data suggest that up-regulation of TSPO level during neuroinflammation may be an adaptive response mechanism, a way to provide more neurosteroids. We confer that TSPO could be an attractive drug target for controlling neuroinflammation in the future.

Keywords: Allopregnanolone; Cognition; Finasteride; Lps; Neuroinflammation; Tspo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CA1 Region, Hippocampal / drug effects
  • CA1 Region, Hippocampal / metabolism*
  • Cognitive Dysfunction / complications
  • Cognitive Dysfunction / metabolism*
  • Encephalitis / chemically induced
  • Encephalitis / complications
  • Encephalitis / metabolism*
  • Finasteride / administration & dosage
  • Genetic Vectors / administration & dosage
  • Lentivirus / physiology
  • Lipopolysaccharides
  • Male
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Pregnanolone / metabolism
  • Progesterone / metabolism
  • Receptors, GABA / metabolism*
  • Up-Regulation / drug effects

Substances

  • Bzrp protein, mouse
  • Lipopolysaccharides
  • Receptors, GABA
  • Progesterone
  • Finasteride
  • Pregnanolone