# Bridging tradition and modernity: mitochondrial dynamics as a Traditional Chinese Medicine therapeutic target in cardiovascular disease

**Authors:** Chengyu Du, You Yu, Meng Li, Jin Zhou, You Wang, Xuefeng Guo, Huan Zhang, Zheng Li, Yelei Han, Min Pang, Rui Yu

PMC · DOI: 10.1186/s13020-025-01225-8 · Chinese Medicine · 2026-02-09

## TL;DR

This paper explores how Traditional Chinese Medicine can target mitochondrial imbalances to treat cardiovascular disease through multi-component therapies.

## Contribution

It introduces a TCM-Mitochondrial Dynamics Intervention Model linking TCM principles with mitochondrial regulation for heart disease.

## Key findings

- TCM formulations like BYHWD and QSYQ modulate mitochondrial fission/fusion proteins Drp1, Mfn2, and OPA1.
- Bioactive compounds such as salidroside and astragaloside IV activate pathways like AMPK/SIRT1 to regulate mitochondria.
- A TCM-MDIM model is proposed to integrate TCM concepts with mitochondrial-level therapeutic strategies.

## Abstract

A pathological link exists between mitochondrial fission/fusion imbalance and cardiovascular disease (CVD). Traditional Chinese Medicine (TCM), based on concepts such as "Qi stagnation and blood stasis" and "Yin-Yang imbalance," helps balance mitochondrial function through the combined effects of multiple components, providing a comprehensive treatment approach for CVD.

To methodically clarify the molecular processes by which TCM formulations, extracts, and bioactive compounds target mitochondrial dynamics to intervene in CVD over the past five years, highlighting their ethnopharmacological significance in "multi-component and multi-target" synergistic actions.

This study searched PubMed, Web of Science, Wanfang, and VIP databases (2019–2024), using the Boolean search formula: ("cardiovascular disease" OR "CVD") AND ("mitochondrial dynamics" OR "mitochondrial fission" OR "mitochondrial fusion") AND ("Traditional Chinese Medicine" OR "TCM") AND ("active compounds" OR "bioactive components"). After deduplication with EndNote, 183 articles were systematically screened and included, comprising in vitro experiments using cardiomyocyte models, in vivo studies based on animal models of CVD, and mechanistic investigations utilizing ex vivo tissues or cellular experiments (all human clinical trials were excluded).

Formulations such as Buyang Huanwu Decoction (BYHWD) and Qishen Yiqi Dropping Pills (QSYQ) improved heart conditions by reducing dynamin-related protein 1 (Drp1) overactivity and increasing mitofusin 2 (Mfn2) and optic atrophy 1 (OPA1) levels. Bioactive compounds, such as salidroside(Sal), prevented Drp1 from causing mitochondria to split apart by activating the AMP-activated protein kinase(AMPK)/Sirtuin 1(SIRT1) pathway, while astragaloside IV facilitated better mitochondrial fusion to enhance energy utilization.

TCM manages mitochondria dynamics through multi-target mechanisms, connecting "overall treatment" with "specific targeting" for heart disease therapy. Further ethnopharmacological translation requires standardized screening of bioactive components and the development of innovative drug delivery systems. The study suggests a "Traditional Chinese Medicine-Mitochondrial Dynamics Intervention Model (TCM-MDIM)," which combines organelle-level mitochondrial regulation with the principle of balancing blood and qi to offer novel approaches to the targeted therapy of cardiovascular disorders.

## Linked entities

- **Genes:** CRMP1 (collapsin response mediator protein 1) [NCBI Gene 1400], MFN2 (mitofusin 2) [NCBI Gene 9927], OPA1 (OPA1 mitochondrial dynamin like GTPase) [NCBI Gene 4976], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], SIRT1 (sirtuin 1) [NCBI Gene 23411]
- **Proteins:** MFN2 (mitofusin 2), SIRT1 (sirtuin 1)
- **Chemicals:** salidroside (PubChem CID 159278), astragaloside IV (PubChem CID 158694)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, MFN2 (mitofusin 2) [NCBI Gene 9927] {aka CMT2A, CMT2A2, CMT2A2A, CMT2A2B, CPRP1, HMSN6A}, OPA1 (OPA1 mitochondrial dynamin like GTPase) [NCBI Gene 4976] {aka BERHS, MGM1, MTDPS14, MTDPS14A, MTDPS14B, NPG}, DNM1L (dynamin 1 like) [NCBI Gene 10059] {aka DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1}
- **Diseases:** heart disease (MESH:D006331), CVD (MESH:D002318), Traditional Chinese (MESH:C562377)
- **Chemicals:** astragaloside IV (MESH:C052064), Sal (-), salidroside (MESH:C009172)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12888643/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12888643/full.md

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Source: https://tomesphere.com/paper/PMC12888643