# Electroacupuncture alleviates Parkinson’s disease by targeting HDAC/SIRT-mediated deacetylation of 14-3-3

**Authors:** Zhao-Qin Wang, Han-Dan Zheng, Ling-Jie Li, Lu-Lu Cao, Lin Shen, Yu Qiao, Yi-Yi Chen, Lu-Yi Wu, Guo-Na Li, Huan-Gan Wu

PMC · DOI: 10.3389/fnagi.2025.1719326 · Frontiers in Aging Neuroscience · 2026-01-14

## TL;DR

Electroacupuncture improves Parkinson's disease symptoms in mice by restoring protein acetylation balance, particularly in the 14-3-3 protein.

## Contribution

This study reveals a novel mechanism by which electroacupuncture alleviates Parkinson's disease through HDAC/SIRT-mediated deacetylation of 14-3-3.

## Key findings

- EA improved motor coordination and sensorimotor function in PD mice.
- EA reduced α-synuclein accumulation and preserved dopaminergic neurons.
- EA reversed hyperacetylation of 14-3-3 by upregulating deacetylase expression.

## Abstract

Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the loss of dopaminergic neurons and the accumulation of pathological α-synuclein. Although current treatments can alleviate symptoms, they do not modify disease progression. Growing evidence implicates gut microbiota dysbiosis and aberrant protein acetylation in PD pathogenesis. Electroacupuncture (EA) has shown therapeutic potential in PD; however, its effects on protein acetylation remain unclear.

A PD mouse model was established through MPTP induction and fecal microbiota transplantation (FMT) from PD patients. Mice received EA stimulation at Baihui (GV20) and Yanglingquan (GB34) acupoints for 14 days. Behavioral tests, immunohistochemistry, Western blot, qPCR, and 4D label-free acetyl proteomics were employed to assess motor function, neuronal integrity, protein expression, and acetylation profiles.

EA significantly improved motor coordination, enhanced sensorimotor function in the adhesive removal test, and increased open-field activity in PD mice. It attenuated the loss of tyrosine hydroxylase–positive neurons and decreased α-synuclein accumulation in the substantia nigra. Proteomic analysis revealed hyperacetylation of Ywhaq (14-3-3) in PD mice, which was reversed by EA. Mechanistically, EA upregulated the expression of deacetylases HDAC1/2/3 and SIRT1/2 at both protein and mRNA levels, restoring acetylation homeostasis.

Electroacupuncture ameliorates behavioral and neuropathological phenotypes in a PD mouse model by restoring deacetylase expression and normalizing protein acetylation, particularly of 14-3-3. Our results underscore the therapeutic potential of EA and highlight acetylation modulation as a promising strategy for PD treatment.

## Linked entities

- **Genes:** YWHAQ (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta) [NCBI Gene 10971]
- **Proteins:** YWHAQ (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta), HDAC1 (histone deacetylase 1), HDAC2 (histone deacetylase 2), HDAC3 (histone deacetylase 3), SIRT1 (sirtuin 1), SIRT2 (sirtuin 2)
- **Diseases:** Parkinson’s disease (MONDO:0005180)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Snca (synuclein, alpha) [NCBI Gene 20617] {aka NACP, alpha-Syn, alphaSYN}, Th (tyrosine hydroxylase) [NCBI Gene 21823]
- **Diseases:** PD (MESH:D010300), neurodegenerative disorder (MESH:D019636), neuropathological (MESH:D009422)
- **Chemicals:** MPTP (MESH:D015632), GB34 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12847356/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847356/full.md

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Source: https://tomesphere.com/paper/PMC12847356