ArticleMolecular biology reports2026
Acteoside alleviates high glucose-induced ROS accumulation and ferroptosis in ARPE-19 cells by activating the NRF2 signaling pathway.
Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
objectiveThe role of Acteoside (ACT) in regulating ferroptosis of retinal pigment epithelial (RPE) cells in diabetic retinopathy (DR) through the NRF2 pathway was investigated.
methodsAn in vitro DR model was constructed by inducing ARPE-19 cells with 33 mmol/L high glucose (HG), and a C57BL/6 mouse DR model was established via intraperitoneal injection of STZ and treated with different doses of ACT. Ferroptosis was assessed using CCK-8 assay, kits, BODIPY-C11 staining, and Western blot. NRF2 nuclear translocation was examined by immunofluorescence. Retinal damage was evaluated by HE staining.
resultsCompared to the NG group, the HG group showed significantly reduced ARPE-19 cell viability, increased intracellular Fe
conclusionACT alleviated HG-induced ROS accumulation and ferroptosis in ARPE-19 cells by activating the NRF2 pathway, and ACT upregulated NRF2 and inhibited ferroptosis in the retina of DR mice, thereby ameliorating retinal injury.
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