# Acer truncatum Bunge seed oil attenuates learning and memory impairment in AD mouse model via modulating gut microbiota and metabolism

**Authors:** Duoduo Ren, Xuejun Chai, Chenyao Xiang, Yongkang Zhao, Penghao Sun, Mengli Wang, Jing Li, Jiayue Wu, Chenju Yi, Shulin Chen, Enyao Li, Shanting Zhao

PMC · DOI: 10.3389/fnut.2026.1757330 · Frontiers in Nutrition · 2026-02-10

## TL;DR

Acer truncatum seed oil improves memory and reduces brain plaques in Alzheimer's mice by changing gut bacteria and boosting beneficial short-chain fatty acids.

## Contribution

This study demonstrates that Acer truncatum seed oil modulates gut microbiota and metabolism to alleviate Alzheimer's-related impairments in mice.

## Key findings

- ASO improves learning, memory, and reduces Aβ deposition in Alzheimer's transgenic mice.
- ASO alters gut microbiota to increase beneficial short-chain fatty acid-producing bacteria.
- Fecal microbiota transplantation and butyrate supplementation also improve cognitive function in these mice.

## Abstract

This study aimed to clarify the neuroprotective effect of Acer truncatum Bunge seed oil (ASO) and its interactions with the gut microbiota in transgenic mice with 5 × Familial Alzheimer's disease (5 × FAD). The AD-transgenic mice were fed with standard diet supplemented with 4% ASO from one to six months of age. The result show that ASO intervention can alleviate learning and memory impairment, enhance motor coordination and endurance, and reduce Aβ deposition in the brains. It also inhibit the proliferation of microglia and astrocytes, decrease the levels of IL-1β, IL-6, and TNF-α in the hippocampus and serum. Then, ASO could increase the Chao1 index and Shannon index, alter the gut microbiota composition, specifically, enhance the growth of gut bacteria correlated with the production of SCFAs, including Ruminococcaceae, Butyricicoccus, Sutterella and others, particularly those related to butyrate production. Additionally, ASO can increase the concentrations of SCFAs in fresh feces and serum, particularly butyric acid. ASO could primarily modulate the biosynthesis of unsaturated fatty acids, glycerophospholipid metabolism, and sphingolipids metabolism in serum. At the same time, Fecal microbiota transplantation (FMT) could reduce Aβ deposition, enhance learning and memory. Finally, Supplementation of sodium Buty also mitigate learning and memory impairments. This study highlights the gut microbiota might be a potential therapeutic target for AD and provides a scientific foundation for developing novel pharmaceuticals or nutraceuticals.

## Linked entities

- **Chemicals:** Aβ (PubChem CID 10246829), IL-6 (PubChem CID 165368475), butyric acid (PubChem CID 264)
- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Genes:** Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, H2-Ab1 (histocompatibility 2, class II antigen A, beta 1) [NCBI Gene 14961] {aka Abeta, H-2Ab, H2-Ab, I-Abeta, IAb, Ia-2}, Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 84027], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Tyms (thymidylate synthase) [NCBI Gene 22171] {aka Ts}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, Thy1 (thymus cell antigen 1, theta) [NCBI Gene 21838] {aka CD90, T25, Thy-1, Thy-1.2, Thy1.1, Thy1.2}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Fancd2 (Fanconi anemia, complementation group D2) [NCBI Gene 211651] {aka 2410150O07Rik, FA-D2, FA4, FACD, FAD, FANCD}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, Vip (vasoactive intestinal polypeptide) [NCBI Gene 22353], Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Diseases:** multiple sclerosis (MESH:D009103), deficits (MESH:D009461), neuropathological (MESH:D009422), cognitive deficits (MESH:D003072), memory deficits (MESH:D008569), neurofibrillary (MESH:D055956), neuronal damage (MESH:D009410), NA (MESH:D011015), FMT (MESH:D005242), deficits in learning and memory (MESH:D007859), amyloid (MESH:C000718787), dementia (MESH:D003704), neurotoxic (MESH:D020258), brain atrophy (MESH:C566985), AD (MESH:D000544), dysbiosis (MESH:D064806), toxicity (MESH:D064420), autism (MESH:D001321), Neuroinflammation (MESH:D000090862), CNS degeneration (MESH:D002493), CNS inflammation (MESH:D007249), neurodegeneration (MESH:D019636), metabolic disturbances (MESH:D024821), Deficiency (MESH:D007153), demyelinating diseases (MESH:D003711), brain disorders (MESH:D001927), mitochondrial dysfunction (MESH:D028361)
- **Chemicals:** SLs (MESH:D013107), OA (MESH:D019301), PB (MESH:D007854), glutamate (MESH:D018698), acetic acid (MESH:D019342), Eicosenoic acid (MESH:C572289), isovaleric acid (MESH:C008216), ROS (MESH:D017382), neomycin (MESH:D009355), sphingosine (MESH:D013110), D-galactose (MESH:D005690), DHA (MESH:C027493), Cer (MESH:D002518), vegetable oils (MESH:D010938), NA (MESH:C013147), SCFA (MESH:D005232), glycine (MESH:D005998), threonine (MESH:D013912), eicosapentaenoic acid (MESH:D015118), Omega-3 (MESH:D010743), LA (MESH:D007811), 2-linoleoylglycerol (MESH:C114955), AlCl3 (MESH:D000077410), Sodium Buty (MESH:D020148), ALA (MESH:D017962), lipid (MESH:D008055), CY (MESH:D003545), C18:0 (MESH:C031183), PFA (MESH:C003043), vancomycin (MESH:D014640), palmitic acid (MESH:D019308), docosahexaenoic acid (MESH:D004281), propionic acid (MESH:C029658), TS (MESH:C009462), beta-glycerophosphate (MESH:C031463), aspartate (MESH:D001224), Buty (MESH:D002087), amino acids (MESH:D000596), EA (MESH:C049811), isobutyric acid (MESH:C020380), lecanemab (MESH:C000612089), serine (MESH:D012694), essential FAs (MESH:D005228), FA (MESH:D005227), Arginine (MESH:D001120), gamma-linolenic acid (MESH:D017965), alanine (MESH:D000409), PC (MESH:D010713), MUFAs (MESH:D005229), streptomycin (MESH:D013307), metronidazole (MESH:D008795), Pc (MESH:C053518), E-EL-H0542 (-), Pe (MESH:C483858), Glycerophosphate (MESH:D005994), valeric acid (MESH:C038780), Helium (MESH:D006371), SM (MESH:D013109), saline (MESH:D012965), cuprizone (MESH:D003471)
- **Species:** Allobaculum (genus) [taxon 174708], Sutterella (genus) [taxon 40544], gut metagenome (species) [taxon 749906], Actinomycetota (actinobacteria, phylum) [taxon 201174], Alicyclobacillus sp. SO (species) [taxon 405202], Acer truncatum (purple-blow maple, species) [taxon 47965], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Butyricicoccus (genus) [taxon 580596], Adlercreutzia (genus) [taxon 447020], Acer (maple trees, genus) [taxon 4022], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Chlamydia (genus) [taxon 810], Streptococcus (genus) [taxon 1301]
- **Mutations:** S0033S, F2163-A, S0101S

## Full text

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## Figures

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## References

76 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929499/full.md

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Source: https://tomesphere.com/paper/PMC12929499