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Published on: January 30, 2014
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.
Abstract:
Parkinson's disease (PD), as a neurologically implemented disease with complex etiological factors, has a complex and variable pathogenesis. Accompanying further research, neuroinflammation has been found to be one of the possible factors in its pathogenesis. Microglia, as intrinsic immune cells in the brain, play an important role in maintaining microenvironmental homeostasis in the brain. However, over-activation of neurotoxic microglia in PD promotes neuroinflammation, which further increases dopaminergic (DA) neuronal damage and exacerbates the disease process. Therefore, targeting and regulating the functional state of microglia is expected to be a potential avenue for PD treatment. In addition, plant extracts have shown great potential in the treatment of neurodegenerative disorders due to their abundant resources, mild effects, and the presence of multiple active ingredients. However, it is worth noting that some natural products have certain toxic side effects, so it is necessary to pay attention to distinguish medicinal ingredients and usage and dosage when using to avoid aggravating the progression of diseases. In this review, the roles of microglia with different functional states in PD and the related pathways inducing microglia to transform into neuroprotective states are described. At the same time, it is discussed that abscisic acid (ABA) may regulate the polarization of microglia by targeting them, promote their transformation into neuroprotective state, reduce the neuroinflammatory response in PD, and provide a new idea for the treatment of PD and the selection of drugs.
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.
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