Effect of Urtica Dioica against Doxorubicin-Induced Cardiotoxicity in Rats through Suppression of Histological Damage, Oxidative Stress and Lipid Peroxidation

被引:8
作者
Erboga, Mustafa [1 ]
Donmez, Yeliz Bozdemir [2 ]
Sener, Umit [3 ]
Erboga, Zeynep Fidanol [1 ]
Aktas, Cevat [1 ]
Kanter, Mehmet [4 ]
机构
[1] Namik Kemal Univ, Sch Med, Dept Histol & Embryol, Tekirdag, Turkey
[2] Namik Kemal Univ, Sch Med, Dept Physiol, Tekirdag, Turkey
[3] Trakya Univ, Technol Res & Dev Applicat & Res Ctr, Edirne, Turkey
[4] Istanbul Medeniyet Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkey
来源
EUROPEAN JOURNAL OF GENERAL MEDICINE | 2016年 / 13卷 / 02期
关键词
Doxorubicin; urtica dioica; cardiotoxicity; oxidative stress; rat;
D O I
10.15197/ejgm.1567
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Doxorubicin (DOX) is a highly effective anti-cancer drug with limited clinical use due to its serious cardiotoxicity. Urtica dioica L. seeds (UD), have been widely used in folk medicine, particularly in the therapy for advanced cancer patients, possesses a potent anti-oxidant properties. The goal of present study was to investigate the cardioprotective effects of UD on DOX-induced cardiotoxicity. Method: The rats in the UD treated group were given intraperitoneally 2 ml/kg UD. To induce cardiotoxicity, 30 mg/kg DOX was injected intraperitoneally by a single dose and the rats were sacrificed after 48 h. Results: The present study revealed for the first time a protective role of UD against DOX-induced cardiotoxicity. UD therapy significantly protected against DOX-induced myocardial damage which was characterized by conduction abnormalities, vacuolization, inflammatory cell infiltration, hemorrhages, and myofibrillar disarrangement. As indicators of oxidative stress, DOX caused significantly increase lipid peroxidation and reduction in activities of antioxidant enzymes; superoxide dismutase, glutathione peroxidase, and catalase. UD treatment significantly attenuated DOX-induced oxidative injury. Conclusion: The present study showed that UD might be a suitable cardioprotector against toxic effects of DOX.
引用
收藏
页码:139 / 144
页数:6
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