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Integrated Model of Endothelial NO Regulation and Systemic Circulation for the Comparison Between Pulsatile and Continuous Perfusion

机译:血管内皮一氧化氮调节与系统循环的集成模型,用于搏动性和持续性灌注的比较

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摘要

Many experimental studies concerning nitric oxide (NO) release from endothelium and its vasodilative action are available in the literature, but no analytical description or modeling of these phenomena can be found. On the contrary, a large modeling literature is available concerning the other cardiovascular control mechanisms, such as the myogenic and metabolic control. In order to analytically describe these phenomena, a model of the endothelial control (defined in the Laplace domain and based on experimental data) was implemented and integrated with a lumped-parameter model of the systemic circulation, consisting of large artery segments and peripheral networks. The endothelial regulation model was based on the hypothesis proposed by Kuchan and Frangos, considering that NO release from the endothelium is generated by two parallel paths. The whole model was then applied to study the different vascular constriction or dilation under continuous or pulsatile perfusion, in order to better understand the clinical evidences of a poor organ perfusion in the presence of continuous with respect to pulsatile cardiopulmonary bypass. According to the experimental evidences, the main results obtained from the model revealed a widespread vascular constriction under continuous perfusion with respect to pulsatile. This result remains constant in the presence of different conditions of blood parameters and flow waveform.
机译:关于内皮中一氧化氮(NO)释放及其血管舒张作用的许多实验研究可在文献中找到,但是找不到这些现象的分析描述或模型。相反,关于其他心血管控制机制(如肌源性和代谢控制)的大量建模文献可供参考。为了分析地描述这些现象,实施了内皮控制模型(在拉普拉斯域中定义并基于实验数据),并与系统循环的集总参数模型集成,该模型由大动脉段和外围网络组成。内皮调节模型基于Kuchan和Frangos提出的假设,考虑到内皮的NO释放是通过两条平行的途径产生的。然后将整个模型用于研究连续或搏动性灌注下不同的血管收缩或扩张,以便更好地了解在连续存在搏动性心肺旁路的情况下器官灌注不佳的临床证据。根据实验证据,从该模型获得的主要结果表明,在连续灌注下,脉动具有广泛的血管收缩。在血液参数和流量波形不同的情况下,该结果保持恒定。

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