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Updated: Jun 27, 2026

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Carvedilol Exerts Cardioprotective Effects Against Doxorubicin Toxicity via Autophagy Modulation and Energetics
Asma Boukhalfa1, Pei-Tsz Shin2, Dawn M Meola2
1Molecular Cardiology Research Institute, Tufts Medical Center, Boston, MA 02111, USA.
Insights
Carvedilol protects the heart from doxorubicin cardiotoxicity by restoring autophagy and mitochondrial function. This study shows carvedilol
Area of Science:
- Cardiology
- Pharmacology
- Oncology
Background:
- Carvedilol is approved for heart failure with reduced ejection fraction.
- Its role in preventing cancer therapy-induced heart failure is unclear.
- Doxorubicin chemotherapy can cause cardiotoxicity.
Purpose of the Study:
- To investigate carvedilol's potential to mitigate doxorubicin cardiotoxicity.
- To evaluate carvedilol's effects independent of clinical confounding factors.
- To assess carvedilol's cardioprotective mechanisms.
Main Methods:
- Used in vitro (cardiomyocytes, cardiac slices) and in vivo (mice, dogs) models.
- Evaluated disease-free and cancer-bearing animals.
- Assessed cardiac function, structure, autophagy, apoptosis, and mitochondrial energetics.
Main Results:
- Carvedilol restored autophagy and prevented apoptosis in cardiac cells.
- It improved mitochondrial energetics across human, canine, and murine models.
- Carvedilol preserved cardiac function and structure in mice and dogs receiving doxorubicin.
Conclusions:
- Carvedilol activates cardioprotective autophagy.
- It prevents doxorubicin-induced cell death and improves cardiac energetics.
- Carvedilol demonstrates cross-species efficacy in mitigating cardiotoxicity.
Abstract:
Background/Objectives: Carvedilol is an adrenergic blocker FDA-approved to improve outcomes in heart failure with reduced ejection fraction. Clinical trials examining whether carvedilol may be cardioprotective in the setting of cancer therapy-induced heart failure have generated mixed results that may depend on the cancer regimen, tumor, or comorbidities. Methods: To investigate the therapeutic potential of carvedilol to mitigate doxorubicin cardiotoxicity in cardiomyocytes, myocardial tissue, and in vivo, independent of confounding factors in clinical studies, we utilized disease-free cardiac slices and cardiomyocytes from mice, dogs, and human in vitro, and in wildtype mice injected with doxorubicin in vivo. We further evaluated the impact of carvedilol in dogs with cancer receiving doxorubicin. Results: In primary canine and murine cardiac slices, carvedilol treatment restored autophagy and prevented apoptosis from doxorubicin. Carvedilol restored mitochondrial energetics in human, canine, and murine models. In wildtype mice challenged with doxorubicin, carvedilol prevented declines in cardiac function and alterations in cardiac structure. In pet dogs with cancer and undergoing doxorubicin treatment, carvedilol was beneficial in preserving cardiac function and structure. Conclusions: Carvedilol activates cardioprotective autophagy, arrests doxorubicin-induced cell death, and improves energetics and cardiac structure and function across species.
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