# Sanshen San Formula Hinders Cognitive Function and Pathology in Alzheimer's Disease Through Potentiating the Function of Synapse

**Authors:** Shiquan Chang, Nana Ding, Yalin Li, Ying Li, Ziling Tang, Junping Pan, Li Yan, Jiaxu Chen

PMC · DOI: 10.1111/cns.70349 · 2025-04-09

## TL;DR

A traditional Chinese herbal formula improves cognitive function and reduces Alzheimer's disease pathology in mice by enhancing synapse and mitochondrial function.

## Contribution

Sanshen San is shown to be a multi-target therapeutic strategy for Alzheimer's disease through synaptic and metabolic mechanisms.

## Key findings

- Sanshen San improves cognitive performance in Aβ1-42-injected and 5xFAD mouse models.
- The formula reduces Aβ plaque burden and enhances microglial phagocytosis.
- SSS restores synaptic integrity and neurotransmitter balance, particularly in the dopaminergic system.

## Abstract

Alzheimer's disease (AD) constitutes a devastating neurodegenerative disorder, manifested by amyloid‐β aggregation, phosphorylated tau accumulation, and progressive cognitive deterioration. Current therapeutic interventions remain predominantly symptomatic, underscoring the urgency for more efficacious treatment strategies.

This study elucidated the therapeutic potential of Sanshen San (SSS), a traditional Chinese herbal formula encompassing Polygala Radix, Pini Radix in Poria, and Acori Tatarinowii Rhizoma, on cognitive function and AD pathology.

We implemented both acute Aβ1‐42‐injected mice and 5xFAD transgenic mouse models. The therapeutic efficacy of SSS was assessed through behavioral paradigms including Y‐maze, Novel Object Recognition, and Morris Water Maze. Molecular mechanisms were delineated utilizing RNA sequencing, metabolomics analysis, immunofluorescence staining, Golgi‐Cox staining, transmission electron microscopy, and Western blotting.

Chemical analysis unveiled 10 principal bioactive compounds in SSS. The formula substantially ameliorated cognitive performance in both Aβ1‐42‐injected and 5xFAD mouse models, attenuated Aβ plaque burden, and augmented microglial phagocytosis. SSS safeguarded synaptic integrity, enhanced mitochondrial function, and facilitated autophagy. Transcriptomic and metabolomic analyses demonstrated that SSS predominantly operates by reinstating synaptic transmission and neurotransmitter function, particularly in the dopaminergic system.

SSS efficaciously mitigates AD pathology through potentiating synaptic function, optimizing mitochondrial homeostasis, and restoring neurotransmitter balance, exemplifying a promising multi‐target therapeutic strategy for the treatment of AD.

SanshenSan formula efficaciously mitigates AD pathology through potentiating synaptic function, optimizing mitochondrial homeostasis, and restoring neurotransmitter balance, exemplifying a promising multi‐target therapeutic strategy for the treatment of Alzheimer's disease.

## Linked entities

- **Proteins:** ab (abrupt), MAPT (microtubule associated protein tau)
- **Diseases:** Alzheimer's disease (MONDO:0004975)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}
- **Diseases:** neurodegenerative disorder (MESH:D019636), AD (MESH:D000544), cognitive deterioration (MESH:D003072)
- **Chemicals:** 5xFAD (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** 5xFAD — Mus musculus (Mouse), Transformed cell line (CVCL_5U93)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11979623/full.md

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Source: https://tomesphere.com/paper/PMC11979623