Cardioprotective mechanisms of phytochemicals against doxorubicin-induced cardiotoxicity

被引:128
作者
Abushouk, Abdelrahman Ibrahim [1 ,2 ]
Ismail, Ammar [2 ,3 ]
Salem, Amr Muhammad Abdo [1 ,2 ]
Afifi, Ahmed M. [1 ]
Abdel-Daim, Mohamed M. [4 ,5 ]
机构
[1] Ain Shams Univ, Fac Med, Cairo, Egypt
[2] NovaMed Med Res Assoc, Cairo, Egypt
[3] Al Azhar Univ, Fac Med, Cairo, Egypt
[4] Suez Canal Univ, Pharmacol Dept, Fac Vet Med, Ismailia 41522, Egypt
[5] Dr DY Patil Med Coll, Pharmacol Dept, Pune, Maharashtra, India
关键词
Cardioprotection; Doxorubicin; Phytochemicals; Toxicity; ADRIAMYCIN-INDUCED CARDIOTOXICITY; INDUCED OXIDATIVE STRESS; INDUCED CARDIAC TOXICITY; AGED GARLIC EXTRACT; INDUCED APOPTOSIS; HEART-FAILURE; IN-VITRO; LIPID-PEROXIDATION; PROTECTIVE ROLE; KAPPA-B;
D O I
10.1016/j.biopha.2017.04.033
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Doxorubicin (DOX) is an anthracycline antibiotic, which is effectively used in the treatment of different malignancies, such as leukemias and lymphomas. Its most serious side effect is dose-dependent cardiotoxicity, which occurs through inducing oxidative stress apoptosis. Due to the myelosuppressive effect of dexrazoxane, a commonly-used drug to alleviate DOX-induced cardiotoxicity, researchers investigated the potential of phytochemicals for prophylaxis and treatment of this condition. Phytochemicals are plant chemicals that have protective or disease preventive properties. Preclinical trials have shown antioxidant properties for several plant extracts, such as those of Aerva lanata, Aronia melanocarpa, Astragalus polysaccharide, and Bombyx mori plants. Other plant extracts showed an ability to inhibit apoptosis, such as those of Astragalus polysaccharide, Azadirachta indica, Bombyx mori, and Allium stavium plants. Unlike synthetic agents, phytochemicals do not impair the clinical activity of DOX and they are particularly safe for long-term use. In this review, we summarized the results of preclinical trials that investigated the cardioprotective effects of phytochemicals against DOX-induced cardiotoxicity. Future human trials are required to translate these cardioprotective mechanisms into practical clinical implications. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:935 / 946
页数:12
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