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Updated: Oct 26, 2025

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Compound Danshen Dripping Pill inhibits doxorubicin or isoproterenol-induced cardiotoxicity
Insights
Compound Danshen Dripping Pill (CDDP) protects against heart failure (HF) by normalizing cardiac function and reducing injury markers. This traditional Chinese medicine shows potential for treating cardiovascular disease and HF.
Area of Science:
- Cardiovascular Research
- Traditional Chinese Medicine
- Pharmacology
Background:
- Heart failure (HF) presents significant morbidity and mortality.
- Compound Danshen Dripping Pill (CDDP) is a widely used Traditional Chinese Medicine for cardiovascular conditions.
Purpose of the Study:
- To investigate the protective effects of CDDP against doxorubicin (DOX) or isoprenaline (ISO)-induced heart failure in mice.
- To elucidate the underlying mechanisms of CDDP's cardioprotective actions.
Main Methods:
- Mice were treated with CDDP followed by DOX or ISO induction of heart failure.
- Cardiac function was assessed using electrocardiography and echocardiography.
- Biochemical parameters, myocardial structure, gene expression (RNAseq, qRT-PCR), and protein levels (Western blot) were analyzed.
Main Results:
- CDDP normalized heart weight changes, HF parameters, and fibrogenesis in DOX/ISO-treated mice.
- CDDP restored left ventricular ejection fraction and fractional shortening impaired by DOX/ISO.
- CDDP inhibited DOX/ISO-induced inflammation, cell apoptosis, and pro-fibrotic molecule expression while enhancing antioxidant enzyme expression.
Conclusions:
- CDDP demonstrates significant cardioprotective effects against various models of myocardial injury.
- CDDP normalizes cardiac function and mitigates pathological changes associated with heart failure.
- These findings suggest CDDP has potential therapeutic applications for treating heart failure.
Abstract:
Heart failure (HF) is the advanced heart disease with high morbidity and mortality. Compound DanShen Dripping Pill (CDDP) is a widely used Traditional Chinese Medicine for cardiovascular disease treatment. Herein, we investigated if CDDP can protect mice against doxorubicin (DOX) or isoprenaline (ISO)-induced HF. After 3 days feeding of normal chow containing CDDP, mice were started DOX or ISO treatment for 4 weeks or 18 days. At the end of treatment, mice were conducted electrocardiogram and echocardiographic test. Blood and heart samples were determined biochemical parameters, myocardial structure and expression of the related molecules. CDDP normalized DOX/ISO-induced heart weight changes, HF parameters and fibrogenesis. The DOX/ISO-impaired left ventricular ejection fraction and fractional shortening were restored by CDDP. Mechanistically, CDDP blocked DOX/ISO-inhibited expression of antioxidant enzymes and DOX/ISO-induced expression of pro-fibrotic molecules, inflammation and cell apoptosis. Additional DOX/ISO-impaired targets in cardiac function but protected by CDDP were identified by RNAseq, qRT-PCR and Western blot. In addition, CDDP protected cardiomyocytes against oxygen-glucose deprivation-induced injuries. Taken together, our study shows that CDDP can protect against myocardial injuries in different models, suggesting its potential application for HF treatment.
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