Journal of Functional Foods· 2026Q1
Peony seed oil alleviates selected cognitive deficits in D-galactose-treated mice
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- Q1SCImago
- 2026year
Short summary
Peony seed oil (PSO) significantly improved cognitive performance in D-galactose-induced cognitive impairment in mice, preserving hippocampal morphology and upregulating key synapse-related genes.
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Key points
- Peony seed oil (PSO) improved cognitive performance in mice with D-galactose-induced impairment.
- PSO administration preserved hippocampal morphology and improved serum oxidative stress indicators.
- PSO upregulated hippocampal mRNA expression of synapse-related genes including Dlg4, Syn1, Slc17a7, Grin1, Grin2b, and Stx1a.
- PSO composition includes 45.60% alpha-linolenic acid, 22.62% linoleic acid, and 17.12% oleic acid.
AI-generated from the title and abstract; the full text is not read.
Abstract
Peony seed oil (PSO) is rich in unsaturated fatty acids, but its effects on cognitive impairment remain unclear. Male C57BL/6J mice received D-galactose (200 mg/kg/day) with or without PSO (2.4, 4.8, or 9.6 mL/kg/day) for 8 weeks. Cognition, hippocampal morphology, serum malondialdehyde and superoxide dismutase, hippocampal synapse-related transcripts, PSO composition, and predictive network pharmacology were assessed. PSO improved Morris water maze and Y-maze performance and was associated with more preserved hippocampal morphology. It also improved serum oxidative stress-related indicators and upregulated hippocampal Dlg4 , Syn1 , Slc17a7 , Grin1 , Grin2b , and Stx1a mRNA. PSO contained 45.60% alpha-linolenic acid, 22.62% linoleic acid, and 17.12% oleic acid. Network analysis generated unvalidated candidate targets and pathways. PSO attenuated D-galactose-induced cognitive deficits, although protein-level, brain oxidative-stress, and mechanistic validation is still required.
The authors' abstract, as published at the source. Journal of Functional Foods, 2026 · DOI ↗
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Field: Cellular and Molecular Neuroscience
Cellular and Molecular NeuroscienceNeuroscience