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Underlying mechanism of effect of Shenfu injection on buerger's disease model rats

机译:沉府注射效果对布尔特氏病模型大鼠的潜在机制

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To study the mechanism underlying the therapeutic effect of Shenfu injection (SFI) on the rat models with buerger's disease or thromboangiitis obliterans (TAO). Adult male Sprague Dawley rats were randomly divided into sham operated group, TAO model group, SFI 2.5 mg/kg (low dose), 5 mg/kg (medium dose) and 10 mg/kg (high dose) groups (n =8). Rats were intravenously administered SFI 2.5, 5 and 10mg/kg or saline once per day for 15 days. TAO model was prepared by injecting sodium laurate into the femoral artery of rats. Then we examined pathologic grading of thrombus, the contents of TXB2, 6-K-PGF1a and TXB2/6-K-PGF1α in plasma following SFI or saline treatment. Higher grades of pathological thrombosis, the increase in the TXB2 content and TXB2/6-K-PGF ratio, as well as the decrease of 6-K-PGF content in TAO model group were observed in our experiments; Compared with TAO model group, SFI treatment significantly reduced the numbers of thrombus formation, the TXB2 content and TXB2/6-K-PGF ratio but increased the 6-K-PGF content. These results first suggest that SFI can cause a significant therapeutic effect on experimental TAO model rats by its inhibiting platelet aggregation and enhancing anti-thrombus function of vessel endothelia.
机译:为了研究潜在的大鼠模型参附注射液(SFI)与伯格氏病或血栓闭塞性脉管炎(TAO)的治疗效果的机制。成年雄性Sprague Dawley大鼠随机分为假手术组,TAO模型组,SFI 2.5毫克/千克(低剂量),5mg / kg的(中等剂量)和10mg / kg的(高剂量)组(n = 8) 。大鼠静脉内给药SFI 2.5,5和10mg / kg或盐水每天一次持续15天。 TAO模型通过注射月桂酸钠到大鼠的股动脉制备。然后我们检查了血栓的病理分级,TXB2,6-K-前列腺素F1a和TXB2 / 6-K-PGF1α在血浆以下SFI或盐水处理的内容。高年级病理血栓形成的,在TXB2含量的增加和TXB2 / 6-K-PGF 比,以及的减少6-K-PGF 内容在TAO模型组在我们的实验中观察到;用TAO模型组相比,SFI治疗显著减少的血栓形成中,TXB2含量和TXB2 / 6-K-PGF 比的数字,但增加了6-K-PGF 内容。这些结果首次表明,SFI可以通过其抑制血小板聚集和促进血管内皮细胞的抗血栓功能造成对实验TAO模型大鼠显著的治疗效果。

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