Curcumin protects rat hippocampal neurons against pseudorabies virus by regulating the BDNF/TrkB pathway

Sci Rep. 2020 Dec 17;10(1):22204. doi: 10.1038/s41598-020-78903-0.

Abstract

Pseudorabies virus (PRV) infection can elicit nervous system disorders. Curcumin has been reported to have neuroprotective effects. However, whether curcumin can protect neurons against PRV infection and the underlying mechanisms remain unclear. In the present study, for the first time, the protective effects of curcumin against PRV-induced oxidative stress, apoptosis, and mitochondrial dysfunction in rat hippocampal neurons and the brain-derived neurotrophic factor (BDNF)/tropomyosin-related kinase B (TrkB) pathway were investigated. Results indicated that PRV with a titer of 3.06 × 106 TCID50 (50% tissue culture infective dose) induced oxidative damage of hippocampal neurons 2 h post-infection and that 10 μM curcumin improved the viability of PRV-infected hippocampal neurons. Blocking the BDNF/TrkB pathway reversed the neuroprotective effects of curcumin, which were imparted by decreasing the PRV-induced upregulation of nitric oxide synthase expression, repressing the PRV-activated mitochondrial apoptotic pathway, and mitochondrial dysfunction. To conclude, curcumin exhibited a neuroprotective role against PRV infection by upregulating the BDNF/TrkB pathway. This study provides insight into the anti-PRV neuroprotective application of curcumin and the underlying mechanism in the prophylaxis and treatment of neurological disorders caused by PRV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antiviral Agents / pharmacology*
  • Apoptosis / drug effects
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cells, Cultured
  • Curcumin / pharmacology*
  • Herpesvirus 1, Suid / drug effects*
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Neuroprotection / drug effects
  • Neuroprotective Agents / pharmacology*
  • Nitric Oxide / metabolism
  • Oxidation-Reduction / drug effects
  • Oxidative Stress / drug effects
  • Pyramidal Cells / drug effects*
  • Pyramidal Cells / metabolism*
  • Pyramidal Cells / virology*
  • Rats
  • Receptor, trkB / metabolism
  • Signal Transduction / drug effects
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Antiviral Agents
  • Brain-Derived Neurotrophic Factor
  • Neuroprotective Agents
  • Nitric Oxide
  • Superoxide Dismutase
  • Ntrk2 protein, rat
  • Receptor, trkB
  • Curcumin