李桂桂, 卞广兴, 任建平, 温利青, 张敏, 吕秋军. 羟基积雪草苷对兔心肌缺血再灌注损伤的保护作用J. 药学学报, 2007, 42(5): 475-480.
引用本文: 李桂桂, 卞广兴, 任建平, 温利青, 张敏, 吕秋军. 羟基积雪草苷对兔心肌缺血再灌注损伤的保护作用J. 药学学报, 2007, 42(5): 475-480.
LI Gui-gui, BIAN Guang-xing, REN Jian-ping, WEN Li-qing, ZHANG Min, Lü Qiu-jun. Protective effect of madecassoside against reperfusion injury after regional ischemia in rabbit heart in vivoJ. Acta Pharmaceutica Sinica, 2007, 42(5): 475-480.
Citation: LI Gui-gui, BIAN Guang-xing, REN Jian-ping, WEN Li-qing, ZHANG Min, Lü Qiu-jun. Protective effect of madecassoside against reperfusion injury after regional ischemia in rabbit heart in vivoJ. Acta Pharmaceutica Sinica, 2007, 42(5): 475-480.

羟基积雪草苷对兔心肌缺血再灌注损伤的保护作用

Protective effect of madecassoside against reperfusion injury after regional ischemia in rabbit heart in vivo

  • 摘要: 研究羟基积雪草苷(madecassoside,MC)对在体兔缺血再灌注损伤的预防保护作用,并初步探讨MC的作用机制。制备兔心肌缺血再灌注损伤(MIRI)模型;缺血前静脉滴注MC,多时间点检测心电图、血流动力学等指标;用定量组织化学染色方法计算心肌梗死面积;检测血清中酶活性及MDA含量;ELISA法测定血清中C反应蛋白(CRP)含量;TUNEL法检测心肌细胞凋亡;SP法检测细胞凋亡相关蛋白Bcl-2。预先给予MC可明显减小左心及全心心肌梗死面积;对心电图有一定的改善作用;并能明显改善心功能,降低LDH及CK的升高程度。并且,MC可明显降低CRP升高程度;升高SOD酶活性,减少MDA含量;可明显抑制MIRI引起的心肌细胞凋亡,使Bcl-2表达上调。MC对心肌缺血再灌注损伤具有明显的预防和保护作用,作用机制可能与抗脂质过氧化物产生、提高SOD活力、抗炎以及抗心肌细胞凋亡有关。

     

    Abstract: This study is to investigate if madecassoside can protect against myocardial reperfusion injury in rabbit heart in vivo. The ischemia reperfusion model was established. Left ventricular function and ECG were monitored at the ischemia and reperfusion period. The infarct areas were expressed as percentage. The levels of LDH, CK, MDA and SOD were measured and C-reactive protein (CRP) in serum was measured by ELISA kit. Cardiomyocyte apoptosis were measured by TUNEL staining. A monoclonal rabbit anti-goat Bcl-2 proteins as primary antibody was used for Bcl-2 immunohistochemical staining. Treatment with madecassoside (3.2, 1.6 and 0.8 mg·kg-1) iv during ischemia reperfusion injury attenuated myocardial damage, that is, characteristic of decreasing infarct size, decreasing LDH and CK release. Activities of SOD were diminished and MDA level increased obviously in control group whereas pretreatment with madecassoside significantly blunted the decrease of SOD activity, markedly reduced the levels of MDA, CRP and cardiomyocyte apoptosis, and upregulated the expression of Bcl-2. Madecassoside has the protective effect against myocardial ischemia reperfusion injury, and effects of anti-lipid peroxidation, enhancement of SOD activity, anti-inflammation and anti-apoptosis.

     

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