Feruloylated oligosaccharides ameliorate MPTP-induced neurotoxicity in mice by activating ERK/CREB/BDNF/TrkB

Yiru Ding1, Meiyu Zhou1, Ruoyin Zheng1

  • 1Department of Physiology, School of Medicine, Jinan University, Guangzhou 510632, China.

Abstract

Insights

Feruloylated oligosaccharides (FOs) protect dopamine neurons and reduce inflammation in a Parkinson's disease mouse model. These findings suggest FOs may be beneficial for Parkinson's disease prevention and treatment.

Area of Science:

  • Neuroscience
  • Pharmacology
  • Biochemistry

Background:

  • Feruloylated oligosaccharides (FOs) are naturally occurring compounds derived from ferulic acid and oligosaccharides.
  • Parkinson's disease (PD) is a neurodegenerative disorder characterized by the loss of dopaminergic neurons and neuroinflammation.

Purpose of the Study:

  • To investigate the neuroprotective potential of FOs in a mouse model of Parkinson's disease.
  • To determine if FOs can inhibit neuroinflammation and promote the survival of nigrostriatal dopamine neurons.

Main Methods:

  • A Parkinson's disease mouse model was established using 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).
  • Mice were treated with FOs (15 and 30 mg/kg) orally.
  • Neuroprotection was assessed using behavioral tests, immunofluorescence, ELISA, qPCR, and Western blot analysis.

Main Results:

  • FOs significantly increased the survival of dopamine neurons in the substantia nigra pars compacta (SNc).
  • FO treatment inhibited glial activation and reduced the production of inflammatory cytokines.
  • Mechanistic studies indicated that FOs activate the ERK/CREB/BDNF/TrkB signaling pathway.

Conclusions:

  • FOs exhibit neuroprotective effects against MPTP-induced neurodegeneration in mice.
  • The anti-neuroinflammatory effects of FOs may be mediated by the ERK/CREB/BDNF/TrkB pathway.
  • FOs show potential as dietary supplements for the prevention and treatment of Parkinson's disease.

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