2005Zhongguo linchuang yaolixue yu zhiliaoxueRequires access

Effects of shenfu injection on nuclear factor-κB during myocardial ischemia/reperfusion injury in rats

Chengyao Wang

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Abstract

AIM: To study the protective effects of shenfu injection on myocardial ischemia/reperfusion (I/R) injury in rats and its potential mechanisms. METHODS: Myocardial ischemia/reperfusion was produced by tying and untying of left anterior descending coronary artery. Ischemia lasted for 30 min and reperfusion for 60 min. Twenty-four healthy male SD rats weighing 230-280 g were randomly divided into three groups (n=8 in each): sham-operation group, I/R group, and shenfu group which the shenfu injection (10 ml·kg -1) were injected intraperitoneally 30 min before ischemia. The plasma concentration of tumor necrosis factor-α (TNF-α), interleukin-6(IL-6) were measured by ELISA. The heart was harvested and levels of the nuclear factor kappaB (NF-κB) activity were determined by Ecl-western blot analysis and ultrastructures were observed by electron microscopy. RESULTS: NF-κB binding activity in myocardial nuclear and the plasma concentration of IL-6, TNF-α were significantly increased in I/R group than that in the sham-operation group (P 0.01), and they were markedly reduced in shenfu group compared with I/R group (P 0.01). In addition, electron microscopic examination showed more serious injury of the myocardium ultrastructure in I/R group, while in shenfu group the myocardial ultrastructure could improve close to normal. CONCLUSION: Shenfu injection can inhibit NF-κB activity in postischemic myocardium and lead to down-regulation of proinflammtory cytokine expression, which may be one of molecular mechanisms of shenfu injection in cardioprotection.

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AIM: To study the protective effects of shenfu injection on myocardial ischemia/reperfusion (I/R) injury in rats and its potential mechanisms. METHODS: Myocardial ischemia/reperfusion was produced by tying and untying of left anterior descending coronary artery. Ischemia lasted for 30 min and reperfusion for 60 min. Twenty-four healthy male SD rats weighing 230-280 g were randomly divided into three groups (n=8 in each): sham-operation group, I/R group, and shenfu group which the shenfu injection (10 ml·kg -1) were injected intraperitoneally 30 min before ischemia. The plasma concentration of tumor necrosis factor-α (TNF-α), interleukin-6(IL-6) were measured by ELISA. The heart was harvested and levels of the nuclear factor kappaB (NF-κB) activity were determined by Ecl-western blot analysis and ultrastructures were observed by electron microscopy. RESULTS: NF-κB binding activity in myocardial nuclear and the plasma concentration of IL-6, TNF-α were significantly increased in I/R group than that in the sham-operation group (P 0.01), and they were markedly reduced in shenfu group compared with I/R group (P 0.01). In addition, electron microscopic examination showed more serious injury of the myocardium ultrastructure in I/R group, while in shenfu group the myocardial ultrastructure could improve close to normal. CONCLUSION: Shenfu injection can inhibit NF-κB activity in postischemic myocardium and lead to down-regulation of proinflammtory cytokine expression, which may be one of molecular mechanisms of shenfu injection in cardioprotection.

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Available abstract

AIM: To study the protective effects of shenfu injection on myocardial ischemia/reperfusion (I/R) injury in rats and its potential mechanisms. METHODS: Myocardial ischemia/reperfusion was produced by tying and untying of left anterior descending coronary artery. Ischemia lasted for 30 min and reperfusion for 60 min. Twenty-four healthy male SD rats weighing 230-280 g were randomly divided into three groups (n=8 in each): sham-operation group, I/R group, and shenfu group which the shenfu injection (10 ml·kg -1) were injected intraperitoneally 30 min before ischemia. The plasma concentration of tumor necrosis factor-α (TNF-α), interleukin-6(IL-6) were measured by ELISA. The heart was harvested and levels of the nuclear factor kappaB (NF-κB) activity were determined by Ecl-western blot analysis and ultrastructures were observed by electron microscopy. RESULTS: NF-κB binding activity in myocardial nuclear and the plasma concentration of IL-6, TNF-α were significantly increased in I/R group than that in the sham-operation group (P 0.01), and they were markedly reduced in shenfu group compared with I/R group (P 0.01). In addition, electron microscopic examination showed more serious injury of the myocardium ultrastructure in I/R group, while in shenfu group the myocardial ultrastructure could improve close to normal. CONCLUSION: Shenfu injection can inhibit NF-κB activity in postischemic myocardium and lead to down-regulation of proinflammtory cytokine expression, which may be one of molecular mechanisms of shenfu injection in cardioprotection.

Key concepts: Ischemia, Cardioprotection, Reperfusion injury, Myocardial ischemia, Tumor necrosis factor alpha, Medicine, Western blot, Artery

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