Schisandrin B Prevents Doxorubicin-Induced Cardiotoxicity via Enhancing Glutathione Redox Cycling

• Published in: Clinical cancer research 2007-11, Vol.13 (22), p.6753-6760
• Main Authors: Li, Ling, Pan, Qiangrong, Han, Weidong, Liu, Zhen, Hu, Xun
• Format: Article
• Language: English
• Subjects: Animals; Anthracyclines - antagonists & inhibitors; Anthracyclines - toxicity; Antibiotics, Antineoplastic - antagonists & inhibitors; Antibiotics, Antineoplastic - toxicity; Antineoplastic agents; Biological and medical sciences; cardiotoxicity; Cyclooctanes - therapeutic use; Doxorubicin; Doxorubicin - antagonists & inhibitors; Doxorubicin - toxicity; drug resistance; Glutathione - metabolism; glutathione redox cycling; Heart Diseases - chemically induced; Heart Diseases - prevention & control; Lignans - therapeutic use; Medical sciences; Mice; Mice, Inbred ICR; Oxidation-Reduction; Pharmacology. Drug treatments; Polycyclic Compounds - therapeutic use; schisandrin B
• ISSN: 1078-0432; 1557-3265
• DOI: 10.1158/1078-0432.CCR-07-1579

Purpose: The dose-cumulative cardiotoxicties and the emerging cancerous apoptotic/drug resistance are two major obstacles limiting the efficacy of anthracycline antibiotics, notably doxorubicin. We attempted to prove if schisandrin B (Sch B), a dual inhibitor of P-glycoprotein and multidrug resistance–associated protein 1, could protect against doxorubicin-induced cardiotoxicity, on the premise that Sch B is an enhancer of glutathione redox cycling that may attenuate doxorubicin-induced oxidative stress in the cardiomyocytes. Experimental Design: Mice or rat were dosed with a single injection of doxorubicin (25 mg/kg, i.p.) with or without pretreatment of Sch B. The protective roles of Sch B against doxorubicin-induced cardiac damage were evaluated on the aspects of the release of cardiac enzymes into serum, the formation of malondialdehyde, the activation of matrix metalloproteinase, the structural damage in the left ventricles, the mortality rates, and the cardiac functions. Results: Pretreatment of Sch B significantly attenuated doxorubicin-induced cardiotoxicities on all the aspects listed above. The underlying mechanism was associated with the effect of Sch B on maintaining the cardiomyocytic glutathione and the activities of superoxide dismutase, and the key enzymes (glutathione peroxidase, glutathione reductase, and glutathione transferase) responsible for glutathione redox cycling, which neutralized doxorubicin-induced oxidative stress. Conclusion: To the best of our knowledge, Sch B is the only molecule ever proved to function as a cardioprotective agent as well as a dual inhibitor of P-glycoprotein and multidrug resistance–associated protein 1, which is potentially applicable to treat cancers, especially the multidrug-resistant cancers involving doxorubicin or its kin.