1. Academic Validation
  2. Compound Danshen Dripping Pill inhibits doxorubicin or isoproterenol-induced cardiotoxicity

Compound Danshen Dripping Pill inhibits doxorubicin or isoproterenol-induced cardiotoxicity

  • Biomed Pharmacother. 2021 Jun:138:111531. doi: 10.1016/j.biopha.2021.111531.
Ke Feng 1 Yuxin Liu 1 Jia Sun 2 Chunlai Zhao 2 Yajun Duan 3 Wenjia Wang 2 Kaijing Yan 4 Xijun Yan 4 He Sun 4 Yunhui Hu 5 Jihong Han 6
Affiliations

Affiliations

  • 1 College of Life Sciences, State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China.
  • 2 GeneNet Pharmaceuticals Co. Ltd., Tianjin, China.
  • 3 Key Laboratory of Metabolism and Regulation for Major Diseases of Anhui Higher Education Institutes, Hefei University of Technology, Hefei, China.
  • 4 GeneNet Pharmaceuticals Co. Ltd., Tianjin, China; The State Key Laboratory of Core Technology in Innovative Chinese Medicine, Tasly Academy, Tasly Holding Group Co., Ltd, Tianjin, China; Tasly Pharmaceutical Group Co., Ltd, Tianjin, China.
  • 5 GeneNet Pharmaceuticals Co. Ltd., Tianjin, China. Electronic address: [email protected].
  • 6 College of Life Sciences, State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China. Electronic address: [email protected].
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.

Keywords

Compound Danshen Dripping Pill (CDDP); Doxorubicin; Heart failure; Isoprenaline.

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