Neuroprotective effect of ketamine against TNF-α-induced necroptosis in hippocampal neurons

J Cell Mol Med. 2021 Apr;25(7):3449-3459. doi: 10.1111/jcmm.16426. Epub 2021 Mar 3.

Abstract

Tumour necrosis factor-α (TNF-α), a crucial cytokine, has various homeostatic and pathogenic bioactivities. The aim of this study was to assess the neuroprotective effect of ketamine against TNF-α-induced motor dysfunction and neuronal necroptosis in male C57BL/6J mice in vivo and HT-22 cell lines in vitro. The behavioural testing results of the present study indicate that ketamine ameliorated TNF-α-induced neurological dysfunction. Moreover, immunohistochemical staining results showed that TNF-α-induced brain dysfunction was caused by necroptosis and microglial activation, which could be attenuated by ketamine pre-treatment inhibiting reactive oxygen species production and mixed lineage kinase domain-like phosphorylation in hippocampal neurons. Therefore, we concluded that ketamine may have neuroprotective effects as a potent inhibitor of necroptosis, which provides a new theoretical and experimental basis for the application of ketamine in TNF-α-induced necroptosis-associated diseases.

Keywords: ketamine; necroptosis; reactive oxygen species; systemic inflammatory response syndrome; tumour necrosis factor-α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Survival
  • Hippocampus / drug effects*
  • Hippocampus / pathology
  • Immunohistochemistry
  • Ketamine / pharmacology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia / drug effects
  • Microglia / metabolism
  • Models, Animal
  • Motor Disorders / chemically induced
  • Motor Disorders / drug therapy*
  • Necrosis / chemically induced
  • Necrosis / drug therapy*
  • Necrosis / pathology
  • Neurons / drug effects*
  • Neurons / pathology
  • Neuroprotective Agents / pharmacology
  • Reactive Oxygen Species / metabolism*
  • Systemic Inflammatory Response Syndrome / drug therapy
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Neuroprotective Agents
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Ketamine