ArticleJournal of translational medicine2025
Stigmasterol exerts antioxidant effects through activation of the Keap1/Nrf2 signaling pathway in Parkinson's disease model.
Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Stigmasterol ameliorates obesity-associated insulin resistance by activating the PPARγ pathway and alleviating oxidative stress.Frontiers in endocrinology · 2026Article
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Authors and funding
6 authors.
Funding
Abstract
backgroundGiven that there is not yet a fully effective treatment for Parkinson's disease (PD), further research into therapeutic agents is necessary to enhance PD patients' clinical performance and quality of life. Stigmasterol (ST) exerts some pharmacological effects on the nervous system, such as antioxidant, anti-apoptosis, anti-inflammation, and modulation of autophagy, but its potential effects on PD are unclear. This study aimed to determine whether ST exerted neuroprotective benefits in a PD model and to clarify the underlying molecular mechanism.
methodsWe performed behavioral, immunohistochemical, immunofluorescence, western blot, and biochemical index assays in 1-methyl-4-phenylpyridinium (MPP
resultsWe found that ST in the PD model activated the Kelch-like ECH-associated protein 1 (Keap1)/nuclear factor-erythroid 2-related factor 2 (Nrf2) signaling pathway and promoted the Nrf2 nuclear translocation. Additionally, it increased the antioxidant enzymes expression, thereby attenuating reactive oxygen species (ROS)-induced oxidative stress, which in turn, slowed the dopaminergic neuron loss by inhibiting apoptotic pathways, and improved the tyrosine hydroxylase (TH) protein expression, and helped reduce motor impairments in the PD mouse model.
conclusionsOur results indicate that ST has an antioxidant role in the PD model through activating the Keap1/Nrf2 signaling pathway, offering a theoretical foundation for its potential therapeutic use in PD treatment.
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