Mol Biol Rep. 2025 Aug 7;52(1):799. doi: 10.1007/s11033-025-10893-6.
ABSTRACT
BACKGROUND: Alzheimer’s disease (AD) is characterized by amyloid-β (Aβ) deposition, which triggers oxidative stress and neuronal damage. Atractylenolide III (AT-III), a plant-derived monomer with antioxidant properties, has shown promise but its neuroprotective effects in AD remain unclear.
METHODS: We established an AD mice model via intracerebroventricular Aβ₁₋₄₂ injection and evaluated AT-III’s neuroprotective effects using behavioral tests, electrophysiological recordings, Western blot, and ELISA. Additionally, we assessed AT-III’s protective effects against hydrogen peroxide (H2O2)-induced oxidative stress in Neuro-2 A (N2A) cells.
RESULTS: AT-III mitigated cognitive and long-term potentiation (LTP) deficits induced by Aβ1-42. It also reduced oxidative stress by decreasing pro-oxidants and increasing anti-oxidants. Furthermore, AT-III activated the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway in the model mice, consequently enhancing the expression of Nrf2, heme oxygenase-1 (HO-1), and superoxide dismutase-1 (SOD-1). In N2A cells, AT-III significantly attenuated H2O2-induced cytotoxicity and oxidative stress, further supporting its role in neuroprotection.
CONCLUSIONS: These results suggest that AT-III may exert neuroprotective effects through antioxidant properties, thereby ameliorating cognitive impairment induced by Aβ1-42. These findings indicate that AT-III could be a potential therapeutic agent for AD.
PMID:40775454 | DOI:10.1007/s11033-025-10893-6
