International journal of molecular sciences · 2026
Propyl Gallate Attenuates Methylglyoxal-Induced Alzheimer-like Cognitive Deficits and Neuroinflammation in Mice.
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Tsai Hui-Yun, Qiu Jing, Liao Han-Wei, Chang Chi-I, Chen Yu-Hsiang, Ho Chi-Tang, Chen Yu-Kuo
Аннотация
Methylglyoxal (MG), a reactive dicarbonyl metabolite associated with diabetes and metabolic disorders, contributes to carbonyl stress, neuroinflammation, and Alzheimer-like neurodegeneration. This study investigated the neuroprotective effects of propyl gallate (PG), a phenolic antioxidant widely used as a food additive, against MG-induced cognitive impairment in mice. Male C57BL/6J mice were exposed to 1% MG in drinking water for eight weeks and orally administered PG (20, 40, or 100 mg/kg/d). Behavioral tests demonstrated that PG significantly improved spatial learning and recognition memory and alleviated anxiety-like behavior induced by MG. Histological and biochemical analyses revealed that PG reduced hippocampal neuronal damage, suppressed tau hyperphosphorylation and amyloid-β (Aβ) accumulation, and attenuated the overexpression of pro-inflammatory cytokines TNF-α and IL-6. Furthermore, PG increased PI3K expression and Akt phosphorylation while reducing activation of GSK-3β, counteracting the MG-induced suppression of this pathway and aligning with reduced tau hyperphosphorylation. These findings indicate that PG protects against MG-related cognitive dysfunction through modulation of neuroinflammatory responses and survival-related signaling pathways, highlighting its potential as a neuroprotective dietary antioxidant for metabolic stress-associated neurodegenerative disorders.
Предметные рубрики MeSH
AnimalsPyruvaldehydeMiceAlzheimer DiseaseMalePropyl GallateCognitive DysfunctionGlycogen Synthase Kinase 3 betaNeuroprotective AgentsMice, Inbred C57BLHippocampustau ProteinsPhosphorylationNeuroinflammatory DiseasesAmyloid beta-PeptidesSignal TransductionPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktDisease Models, Animal