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Cell-cell interaction in blood flow in patients with coronary heart disease (in vitro study)

机译:冠心病患者血流中的细胞 - 细胞相互作用(体外研究)

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Blood cell-cell and cell-vessel wall interactions are one of the key patterns in blood and vascular pathophysiology. We have chosen the method of reconstruction of pulsative blood flow in vitro in the experimental set. Blood flow structure was studied by PC integrated video camera with following slide by slide analysis. Studied flow was of constant volumetric blood flow velocity (1 ml/h). Diameter of tube in use was comparable with coronary arteries diameter. Glucose solution and unfractured heparin were used as the nonspecial irritants of studied flow. Erythrocytes space structure in flow differs in all groups of patients in our study (men with stable angina pectoris (SAP), myocardial infarction (MI) and practically healthy men (PHM). Intensity of erythrocytes aggregate formation was maximal in patients with SAP, but time of their "construction/deconstruction" at glucose injection was minimal. Phenomena of primary clotting formation in patients with SAP of high function class was reconstructed under experimental conditions. Heparin injection (10 000 ED) increased linear blood flow velocity both in patients with SAP, MI and PHP but modulated the cell profile in the flow. Received data correspond with results of animal model studies and noninvasive blood flow studies in human. Results of our study reveal differences in blood flow structure in patients with coronary heart disease and PHP under irritating conditions as the possible framework of metabolic model of coronary blood flow destabilization.
机译:血细胞 - 细胞和细胞 - 血管壁相互作用是血液和血管病理生理学的关键模式之一。我们选择了实验组体外重建脉动血流的方法。通过PC集成摄像机研究了血流结构,通过滑动分析。研究流动是恒定的体积血流速度(1mL / h)。使用中的管子直径与冠状动脉直径相当。葡萄糖溶液和未裂变的肝素被用作研究流动的非特异性刺激物。流动的红细胞空间结构在我们的研究中的所有患者中(具有稳定的心绞痛(SAP),心肌梗死(MI)和实际健康男性(PHM)的男性。红细胞聚集体形成的强度是SAP患者的最大,但是在葡萄糖注射时的“建筑/解构”的时间最小。在实验条件下重建了高函数类别患者初级凝血形成的现象。肝素注射(10 000 ED)患有SAP患者的线性血流速度增加,MI和PHP但调制流量中的细胞轮廓。接收的数据对应于人类的动物模型研究和非血液流动研究的结果。我们的研究结果揭示了冠心病患者血流结构的差异作为冠状动脉血流不稳定的代谢模型可能框架的条件。

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