# NeuproGemp, a polyphenol-rich botanical formula, ameliorates Alzheimer’s-like pathology in APP/PS1 mice via inhibition of human glutaminyl cyclase

**Authors:** Tien-Sheng Tseng, Chia-Ching Liaw, Young-Ji Shiao, Ya-I Huang, Yu-Hsiu Cheng, Wang-Chuan Chen, Keng-Chang Tsai

PMC · DOI: 10.3389/fphar.2025.1673532 · Frontiers in Pharmacology · 2025-10-21

## TL;DR

NeuproGemp, a plant-based formula, reduces Alzheimer's-like symptoms in mice by inhibiting a key enzyme involved in amyloid formation.

## Contribution

NeuproGemp is shown to inhibit human glutaminyl cyclase, offering a novel multi-target botanical approach for Alzheimer's.

## Key findings

- NeuproGemp improved burrowing behavior and reduced escape latency in Alzheimer's mice.
- The formula reduced Aβ1-42 and pE-Aβ3-42 levels and decreased plaque-associated gliosis.
- Pentagalloylglucose, a key compound in NeuproGemp, strongly inhibits human glutaminyl cyclase.

## Abstract

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by cognitive decline and amyloid-β (Aβ) accumulation. Increasing evidence suggests that dietary bioactive compounds may modulate neurodegenerative processes. Here, we evaluated the neuroprotective potential of NeuproGemp, a traditional Chinese functional food formula composed of Gastrodia elata, Paeoniae Radix Rubra, and the immunomodulatory protein GMI from Ganoderma microsporum, in APP/PS1 transgenic mice. Oral supplementation (300 mg/kg/day, 6–8 weeks) significantly improved ethological behaviors, including a ∼150% enhancement in burrowing performance (150 ± 25 g vs. 60 ± 40 g in controls), and reduced escape latency in the Morris water maze (Day 4: p < 0.05; Day 6: p < 0.01). Histological analyses demonstrated attenuated plaque-associated gliosis, with microglial/astroglial clusters reduced from 95 ± 22 to 55 ± 11 per section (p < 0.01), alongside increased hippocampal neurogenesis (DCX + cells: 49 vs. 18 cells/mm, p < 0.001). ELISA revealed reductions of ∼30% in soluble Aβ1-42 and ∼50% in pyroglutamate-modified Aβ3-42 (pE-Aβ3-42). High-performance liquid chromatography identified pentagalloylglucose (PGG) as the principal polyphenolic constituent of Paeoniae Radix Rubra, which exhibited potent human glutaminyl cyclase (hQC) inhibition (IC50 = 0.09 μM; KD = 63.7 nM). Molecular modeling and dynamics simulations further supported stable binding interactions of PGG and tannic acid with hQC. Collectively, these findings indicate that NeuproGemp, enriched in neuroactive polyphenols, exerts multi-targeted modulation of amyloidogenic pathways and represents a promising botanical intervention for mitigating AD-related neuropathology.

## Linked entities

- **Proteins:** GMI (GEM interacting protein), DCX (doublecortin)
- **Chemicals:** pentagalloylglucose (PubChem CID 65238), tannic acid (PubChem CID 16129778)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)
- **Species:** Gastrodia elata (taxon 91201), Ganoderma microsporum (taxon 34462)

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, DCX (doublecortin) [NCBI Gene 1641] {aka DBCN, DC, LISX, SCLH, XLIS}, QPCT (glutaminyl-peptide cyclotransferase) [NCBI Gene 25797] {aka GCT, QC, sQC}, PSEN1 (presenilin 1) [NCBI Gene 5663] {aka ACNINV3, AD3, CMD1U, FAD, PS-1, PS1}
- **Diseases:** AD (MESH:D000544), gliosis (MESH:D005911), neurodegenerative disorder (MESH:D019636), cognitive decline (MESH:D003072)
- **Chemicals:** PGG (MESH:C435084), polyphenol (MESH:D059808), NeuproGemp (-), pyroglutamate (MESH:D011761)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Gastrodia elata (species) [taxon 91201], Ganoderma microsporum (species) [taxon 34462]
- **Cell lines:** pE — Homo sapiens (Human), Transformed cell line (CVCL_6D81)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12582971/full.md

## References

134 references — full list in the complete paper: https://tomesphere.com/paper/PMC12582971/full.md

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Source: https://tomesphere.com/paper/PMC12582971