CoMPLEX, University College London, London, UK.
Medical Physics and Bioengineering, University College London Hospitals, London, UK.
Adv Exp Med Biol. 2013;789:339-344. doi: 10.1007/978-1-4614-7411-1_45.
We have developed a computational model to simulate hypoxia-ischaemia (HI) in the neonatal piglet brain. It has been extended from a previous model by adding the simulation of carotid artery occlusion and including pH changes in the cytoplasm. Here, simulations from the model are compared with near-infrared spectroscopy (NIRS) and phosphorus magnetic resonance spectroscopy (MRS) measurements from two piglets during HI and short-term recovery. One of these piglets showed incomplete recovery after HI, and this is modelled by considering some of the cells to be dead. This is consistent with the results from MRS and the redox state of cytochrome-c-oxidase as measured by NIRS. However, the simulations do not match the NIRS haemoglobin measurements. The model therefore predicts that further physiological changes must also be taking place if the hypothesis of dead cells is correct.
我们开发了一种计算模型来模拟新生仔猪脑的缺氧缺血(HI)。它通过模拟颈总动脉闭塞和细胞质中 pH 值的变化,从以前的模型中扩展而来。在此,将模型模拟与来自 2 只 HI 和短期恢复期间仔猪的近红外光谱(NIRS)和磷磁共振光谱(MRS)测量进行比较。其中一只仔猪在 HI 后表现出不完全恢复,这通过考虑一些细胞死亡来建模。这与 MRS 的结果以及 NIRS 测量的细胞色素 c 氧化酶的氧化还原状态一致。然而,模拟结果与 NIRS 血红蛋白测量值不匹配。因此,如果假设细胞死亡,模型预测还必须发生进一步的生理变化。