黄芪甲素
丙二醛
乳酸脱氢酶
谷胱甘肽
肌酸激酶
再灌注损伤
超氧化物歧化酶
药理学
活性氧
谷胱甘肽过氧化物酶
化学
内科学
缺血
医学
内分泌学
氧化应激
生物化学
酶
抗氧化剂
槲皮素
山奈酚
作者
Daoxu Qu,Jichun Han,Huanhuan Ren,Wenxiao Yang,Xinjie Zhang,Qiusheng Zheng,Dong Wang
摘要
This study aims to evaluate the cardioprotective effects of astragalin against myocardial ischemia/reperfusion (I/R) injury in isolated rat heart. The cardioprotective effects of astragalin on myocardial I/R injury were investigated on Langendorff apparatus. Adult male Sprague-Dawley rats were randomly divided into five groups. The results showed that astragalin pretreatment improved myocardial function. Compared with I/R group, lactate dehydrogenase (LDH) and creatine kinase (CK) activities in coronary flow decreased in astragalin pretreatment groups, whereas superoxide dismutase (SOD) activity and glutathione/glutathione disulfide (GSH/GSSG) ratio significantly increased. The levels of malondialdehyde (MDA), intracellular reactive oxygen species (ROS), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) decreased in astragalin-treated groups. The infarct size (IS) and apoptosis rate in hearts from astragalin-treated groups were lower than those in hearts from the I/R group. Western blot analysis also revealed that astragalin preconditioning significantly reduced Bax level, whereas Bcl-2 was increased in the myocardium. Therefore, astragalin exhibited cardioprotective effects via its antioxidative, antiapoptotic, and anti-inflammatory activities.
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