实验中对促静脉药物疗效的比较研究

D. I. Pozdnyakov, V. V. Kozlova, A. A. Karmanovich, I. E. Rybalko
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引用次数: 1

摘要

介绍。慢性静脉疾病是一组常见的疾病,有显著的并发症风险,需要及时纠正。通常,以类黄酮复合物为基础的促静脉药物用于治疗和预防静脉疾病。评价各种促静脉药物治疗实验性慢性静脉功能不全的疗效。材料和方法。采用股深静脉局部狭窄法造模Wistar大鼠静脉曲张。所研究的药物在手术后30天内口服。在工作过程中,评估了以下参数的变化:皮肤局部血流动力学速率,血管通透性程度,血管壁促炎细胞因子(TNF-α, IL-6)和基质金属蛋白酶9 (MMP9)的浓度。采用超声多普勒术评估局部血流率。Miles试验采用Evans蓝染料外渗程度研究血管通透性的变化。采用酶联免疫分析法测定促炎细胞因子和MMR9的含量。对结果进行统计学处理。该研究表明,与未治疗的动物相比,口服所有研究的静脉导通药物的过程导致血流动力学的恢复和血管通透性的显著降低(p小于0.05)。值得注意的是,与其他研究药物相比,使用微化纯化类黄酮成分1有助于形成更明显的血管效应,这反映在血液流速的增加和血管通透性的降低上。同时,动物给药微量纯化黄酮类化合物1后,促炎细胞因子的浓度有统计学意义的降低,这是其他药物没有观察到的。微量纯化类黄酮组分1的过程管理导致显着的增血作用的发展,表现在微循环的恢复,血管壁炎症的减少。
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Comparative study of the effectiveness of phlebotonic drugs in the experiment
Introduction. Chronic venous diseases are a common group of diseases with a significant risk of complications requiring timely correction. As a rule, phlebotonic drugs based on flavonoid complexes are used for the treatment and prevention of venous diseases.Aim. To evaluate the effectiveness of the use of various phlebotonic drugs in the conditions of experimental chronic venous insufficiency.Materials and methods. Varicose veins were modeled in Wistar rats by partial stricture of the deep femoral vein. The studied medicines were administered orally in a course of 30 days from the moment of surgery. During the work, the change in the following parameters was evaluated: the rate oflocal blood flow in the skin in dynamics, the degree of vascular permeability, the concentration of proinflammatory cytokines (TNF-α, IL-6) and matrix metalloproteinase 9 (MMP9) in the vascular wall. The rate of local blood flow was assessed by ultrasound Dopplerography. The change of vascular permeability was studied by the degree of extravasation of the Evans blue dye in the Miles test. The content of proinflammatory cytokines and MMR9 was determined by enzyme-linked immunoassay. The results were statistically processed.Results. The study showed that the course oral administration of all the studied venotonizing drugs led to the restoration of hemodynamics and a significant (p˂ 0.05) decrease in the degree of vascular permeability in relation to untreated animals. It is worth noting that the use of a micronised purified flavonoid fraction 1 contributed to the development of a more pronounced vasal effect, which was reflected in an increase in blood flow velocity and a decrease in vascular permeability compared to the rest of the studied drugs. At the same time, the administration of micronised purified flavonoid fraction 1 to animals led to a statistically significant decrease in the concentration of proinflammatory cytokines, which was not observed when using other drugs.Conclusion. The course administration of the micronised purified flavonoid fraction 1leads to the development of a pronounced phlebotonic effect, expressed in the restoration of microcirculation, a decrease of the inflammation in the vascular wall. 
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