Resveratrol treatment protects against doxorubicin-induced cardiotoxicity by alleviating oxidative damage

被引:135
作者
Tatlidede, Elif [1 ]
Sehirli, Oezer [1 ]
Velioglu-Ogunc, Ayliz [2 ]
Cetinel, Sule [3 ]
Yegen, Berrak C. [4 ]
Yarat, Aysen [5 ]
Suleymanoglu, Selami [6 ]
Sener, Goeksel [1 ]
机构
[1] Marmara Univ, Sch Pharm, Tibbiye Cad, Dept Pharmacol, TR-34668 Istanbul, Turkey
[2] Marmara Univ, Vocat Sch Hlth Related Profess, TR-34668 Istanbul, Turkey
[3] Marmara Univ, Sch Med, Dept Histol & Embryol, TR-34668 Istanbul, Turkey
[4] Marmara Univ, Dept Physiol, TR-34668 Istanbul, Turkey
[5] Marmara Univ, Sch Dent, Dept Biochem, TR-34668 Istanbul, Turkey
[6] Gulhane Mil Med Acad, Dept Pediat Cardiol, Istanbul, Turkey
关键词
Doxorubicin; toxicity; resveratrol; free radical; ADRIAMYCIN-INDUCED CARDIOMYOPATHY; RED WINE; NITRIC-OXIDE; MOLECULAR-MECHANISM; ANTIOXIDANT ENZYMES; LIPID-PEROXIDATION; CARDIAC TOXICITY; STRESS; DNA; MYELOPEROXIDASE;
D O I
10.1080/10715760802673008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The possible protective effects of resveratrol (RVT) against cardiotoxicity were investigated in Wistar albino rats treated with saline, saline+doxorubicin (DOX; 20 mg/kg) or RVT (10 mg/kg)+DOX. Blood pressure and heart rate were recorded on the 1st week and on the 7th week, while cardiomyopathy was assessed using transthoracic echocardiography before the rats were decapitated. DOX-induced cardiotoxicity resulted in decreased blood pressure and heart rate, but lactate dehydrogenase, creatine phosphokinase, total cholesterol, triglyceride, aspartate aminotransferase and 8-OHdG levels were increased in plasma. Moreover, DOX caused a significant decrease in plasma total antioxidant capacity along with a reduction in cardiac superoxide dismutase, catalase and Na+,K+-ATPase activities and glutathione contents, while malondialdehyde, myelopreoxidase activity and the generation of reactive oxygen species were increased in the cardiac tissue. On the other hand, RVT markedly ameliorated the severity of cardiac dysfunction, while all oxidant responses were prevented; implicating that RVT may be of therapeutic use in preventing oxidative stress due to DOX toxicity.
引用
收藏
页码:195 / 205
页数:11
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