心脏毒性
阿霉素
脂质过氧化
药理学
谷胱甘肽过氧化物酶
抗氧化剂
医学
氧化应激
化学
超氧化物歧化酶
毒性
内科学
化疗
生物化学
作者
M.U.R. Naidu,K. Vijay Kumar,Iyyapu Krishna Mohan,Sundaram Challa,Singh Shashi
出处
期刊:PubMed
日期:2002-08-01
卷期号:40 (8): 894-900
被引量:36
摘要
Doxorubicin (DXR) causes dose dependent cardiotoxicity in experimental animals and in humans. In chronic doxorubicin cardiotoxicity model mice, the role of G. biloba extract (Gbe) which has an antioxidant property, was investigated. Doxorubicin treated animals showed higher mortality (68%), increased ascites, marked bradycardia, prolongation of ST and QT intervals and widening of QRS complex. Myocardial SOD and glutathione peroxidase activity were decreased and lipid peroxidation was increased. Ultrastructure of heart of DXR treated animals showed loss of myofibrils, swelling of mitochondria, vacuolization of mitochondria. G. biloba extract significantly protected the mice from cardiotoxic effects of doxorubicin as evidenced by lowered mortality, ascites, myocardial lipid peroxidation, normalization of antioxidant enzymes, reversal of ECG changes and minimal ultrastructural damage of the heart. The results indicate that administration of G. biloba extract protected mice from doxorubicin-induced cardiotoxicity.
科研通智能强力驱动
Strongly Powered by AbleSci AI