Key result
Compound DanShen Dripping Pill protected mice against doxorubicin or isoprenaline-induced heart failure by restoring left ventricular ejection fraction and fractional shortening.
Why the study?
Heart failure carries high morbidity and mortality, and the authors investigated whether Compound DanShen Dripping Pill could protect against doxorubicin- or isoprenaline-induced heart failure.
Does Compound DanShen Dripping Pill protect against doxorubicin or isoprenaline-induced cardiotoxicity in mice?
Does Compound DanShen Dripping Pill protect against doxorubicin or isoprenaline-induced cardiotoxicity in mice?
Compound DanShen Dripping Pill protects against doxorubicin and isoprenaline-induced cardiotoxicity and heart failure in murine models.
Answers are grounded in this paper and cite their sources.
May support murine cardioprotection; hypothesis-generating for human doxorubicin cardiotoxicity trials.
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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Feng et al. (2021) studied Doxorubicin or isoprenaline-induced heart failure. Compound DanShen Dripping Pill (CDDP) vs. Doxorubicin or isoprenaline alone was evaluated on Heart weight changes, HF parameters, fibrogenesis, LVEF, and fractional shortening. Compound DanShen Dripping Pill protected mice against doxorubicin or isoprenaline-induced heart failure by restoring left ventricular ejection fraction and fractional shortening.
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