Function and Mechanism of Abscisic Acid on Microglia-Induced Neuroinflammation in Parkinson's Disease

Tingting Han1, Yuxiang Xu1, Haixuan Liu1

  • 1Institute for Brain Sciences Research, School of Life Sciences, Henan University, Kaifeng 475004, China.

Insights

Neuroinflammation contributes to Parkinson's disease (PD) pathogenesis. Targeting microglia polarization with abscisic acid (ABA) may offer a novel therapeutic strategy for PD by reducing neuroinflammation and protecting dopaminergic neurons.

Area of Science:

  • Neuroscience
  • Immunology
  • Pharmacology

Background:

  • Parkinson's disease (PD) pathogenesis involves complex etiological factors, with neuroinflammation emerging as a key contributor.
  • Microglia, the brain's intrinsic immune cells, play a dual role; their over-activation in PD exacerbates dopaminergic neuronal damage via neuroinflammation.

Purpose of the Study:

  • To review the roles of microglia in different functional states within PD pathogenesis.
  • To explore pathways that induce microglia to adopt neuroprotective states.
  • To discuss abscisic acid (ABA) as a potential therapeutic agent for modulating microglial polarization in PD.

Main Methods:

  • Literature review focusing on microglial function in PD.
  • Analysis of pathways involved in microglial polarization.
  • Examination of plant extracts, specifically abscisic acid, for therapeutic potential in neurodegenerative disorders.

Main Results:

  • Over-activated microglia promote neuroinflammation, worsening PD progression.
  • Targeting microglial functional states presents a promising therapeutic avenue for PD.
  • Abscisic acid (ABA) shows potential in regulating microglial polarization towards a neuroprotective phenotype.

Conclusions:

  • Modulating microglial polarization is a viable strategy for PD treatment.
  • Abscisic acid (ABA) may reduce PD-associated neuroinflammation by promoting neuroprotective microglia.
  • This research offers new insights for PD drug development and treatment selection.