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January 6, 2026International Journal of Molecular Sciences3 citationsOpen Access

Propyl Gallate Attenuates Methylglyoxal-Induced Alzheimer-like Cognitive Deficits and Neuroinflammation in Mice

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HTHui-Yun TsaiJQJing QiuHLHan-Wei Liao

Key Points

  • The study aims to assess the protective effects of propyl gallate against methylglyoxal-induced cognitive impairment and neuroinflammation.
  • Mice were administered 1% methylglyoxal in drinking water for eight weeks.
  • Propyl gallate was given orally at doses of 20, 40, or 100 mg/kg/d.
  • Behavioral tests evaluated spatial learning, recognition memory, and anxiety-like behavior.
  • Histological and biochemical analyses quantified neuronal damage and inflammatory markers.
  • Propyl gallate significantly improved learning and memory in mice exposed to methylglyoxal.
  • Treatment reduced tau hyperphosphorylation and amyloid-β accumulation in the hippocampus.
  • Propyl gallate decreased levels of pro-inflammatory cytokines IL-6 and TNF-α.

Abstract

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.

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Cite This Study

Tsai et al. (2026) studied this question.

synapsesocial.com/papers/695d8e5f3483e917927a55e0https://doi.org/10.3390/ijms27010511
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