Protective effect of bilberry (Vaccinium myrtillus) against doxorubicin-induced oxidative cardiotoxicity in rats

被引:33
作者
Ashour, Osama M. [2 ]
Elberry, Ahmed A. [1 ,3 ]
Alahdal, Abdulrahman M. [1 ,3 ]
Al Mohamadi, Ameen M. [1 ,3 ]
Nagy, Ayman A. [4 ,5 ]
Abdel-Naim, Ashraf B. [2 ]
Abdel-Sattar, Essam A. [6 ]
Mohamadin, Ahmed M. [7 ]
机构
[1] King Abdulaziz Univ, Fac Pharm, Dept Clin Pharm, Jeddah 21589, Saudi Arabia
[2] King Abdulaziz Univ, Fac Pharm, Dept Pharmacol & Toxicol, Jeddah 21589, Saudi Arabia
[3] Beni Suef Univ, Fac Med, Dept Pharmacol, Bani Suwayf, Egypt
[4] King Abdulaziz Univ, Fac Med, Dept Pathol, Jeddah 21589, Saudi Arabia
[5] Tanta Univ, Fac Med, Dept Forens Med & Clin Toxicol, Tanta, Egypt
[6] King Abdulaziz Univ, Fac Pharm, Dept Nat Prod, Jeddah 21589, Saudi Arabia
[7] Taibah Univ, Fac Med, Dept Clin Biochem, Madinah, Saudi Arabia
来源
MEDICAL SCIENCE MONITOR | 2011年 / 17卷 / 04期
关键词
bilberry; doxorubicin; cardiotoxicity; antioxidant; rats; ANTIOXIDANT ACTIVITY; ADRIAMYCIN; CARDIOMYOPATHY; GLUTATHIONE; CANCER; ACID; INHIBITION; PREVENTION; CRANBERRY; MELATONIN;
D O I
10.12659/MSM.881711
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Doxorubicin (DOX) is a commonly used chemotherapeutic agent. It is associated with serious dose-limiting cardiotoxicity, which is at least partly caused by generation of reactive oxygen species (ROS). Supplementations with bilberries were effective in reducing oxidative stress in many tissue injuries due their high content of antioxidants. The present study investigated the potential protective effect of bilberry extract against DOX-induced cardiotoxicity in rats. Material/Methods: Rats were treated orally with a methanolic extract of bilberry for 10 days. DOX was injected intraperitoneally on day 7. Twenty-four hours after the last bilberry administration, rats were subjected to ECG study. Blood was then withdrawn and cardiac tissues were dissected for assessment of oxidative stress and cardiac tissue injury. Cardiac tissues were also subjected to histopathological examination. Results: Bilberry extract significantly inhibited DOX-provoked reduced glutathione depletion and accumulation of oxidized glutathione, malondialdehyde and protein carbonyls in cardiac tissues. This was accompanied by significant amelioration of reduced cardiac catalase, superoxide dismutase, and glutathione peroxidase activities; and increased cardiac myeloperoxidase activity in response to DOX challenge. Pretreatment with bilberry significantly guarded against DOX-induced increase in serum activities of lactate dehydrogenase, creatine phosphokinase and creatine kinase-MB, as well as the level of troponin I. Bilberry alleviated ECG changes in rats treated with DOX and attenuated its pathological changes. Conclusions: Bilberry protects against DOX-induced cardiotoxicity in rats. This can be attributed, at least in part, to its antioxidant activity.
引用
收藏
页码:BR110 / BR115
页数:6
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