Dronne Marie-Aimée, Boissel Jean-Pierre, Grenier Emmanuel, Gilquin Hervé, Cucherat Michel, Hommel Marc, Barbier Emmanuel, Bricca Giampiero
Service de Pharmacologie Clinique, EA 643,Faculté de Médecine Laënnec, Université Claude Bernard, Lyon, France.
Acta Biotheor. 2004;52(4):255-72. doi: 10.1023/B:ACBI.0000046597.53669.ff.
Understanding the mechanisms and the time and spatial evolution of penumbra following an ischemic stroke is crucially important for developing therapeutics aimed at preventing this area from evolving towards infarction. To help in integrating the available data, we decided to build a formal model. We first collected and categorised the major available evidence from animal models and human observations and summarized this knowledge in a flow-chart with the potential key components of an evolving stroke. Components were grouped in ten sub-models that could be modelled and tested independently: the sub-models of tissue reactions, ionic movements, oedema development, glutamate excitotoxicity, spreading depression, NO synthesis, inflammation, necrosis, apoptosis, and reperfusion. Then, we figured out markers, identified mediators and chose the level of complexity to model these sub-models. We first applied this integrative approach to build a model based on cytotoxic oedema development following a stroke. Although this model includes only three sub-models and would need to integrate more mechanisms in each of these sub-models, the characteristics and the time and spatial evolution of penumbra obtained by simulation are qualitatively and, to some extent, quantitatively consistent with those observed using medical imaging after a permanent occlusion or after an occlusion followed by a reperfusion.
了解缺血性中风后半暗带的机制以及时间和空间演变对于开发旨在防止该区域演变为梗死的治疗方法至关重要。为了帮助整合现有数据,我们决定构建一个形式模型。我们首先收集并分类了来自动物模型和人体观察的主要现有证据,并将这些知识总结在一个流程图中,该流程图包含了正在发展的中风的潜在关键组成部分。这些组成部分被分组为十个可以独立建模和测试的子模型:组织反应、离子运动、水肿发展、谷氨酸兴奋性毒性、扩散性抑制、一氧化氮合成、炎症、坏死、凋亡和再灌注的子模型。然后,我们确定了标志物,识别了介质,并选择了对这些子模型进行建模的复杂程度。我们首先应用这种综合方法构建了一个基于中风后细胞毒性水肿发展的模型。虽然这个模型只包括三个子模型,并且需要在每个子模型中整合更多机制,但通过模拟获得的半暗带的特征以及时间和空间演变在定性上以及在一定程度上在定量上与在永久性闭塞或闭塞后再灌注后使用医学成像观察到的结果一致。