Department of Medical Physics and Biomedical Engineering, University College London, London, UK.
The Human Performance Group, QinetiQ PLC, Farnborough, UK.
Adv Exp Med Biol. 2020;1232:339-345. doi: 10.1007/978-3-030-34461-0_43.
We used a miniature broadband NIRS system to monitor concentration changes in brain oxygenation (oxy- and deoxy- haemoglobin [HbO], [HHb]) and oxidised cytochrome-c-oxidase ([oxCCO]) during a high +Gz acceleration, induced by a human centrifuge, on two healthy experienced volunteers (2 male, 34 and 37 years). We performed a sequence of several +Gz exposures that were terminated at the onset of visual symptoms (loss of peripheral vision). Systemic parameters were recorded (i.e. heart rate, blood pressure and arterial saturation), and brain tissue blood volume changes ([HbT] = [HbO] + [HHb]) and oxygen delivery ([HbDiff] = [HbO] - [HHb]) were calculated. Volunteer 1 demonstrated a decrease in [HbT] of -3.49 ± 0.02 μMol and [HbDiff] of -3.23 ± 0.44 μMol, and an increase of [oxCCO] of 0.42 ± 0.01μMol. Volunteer 2 demonstrated a decrease in [HbDiff] of -4.37 ± 0.23 μMol, and no significant change in [HbT] (0.53 ± 0.06 μMol) and [oxCCO] (0.09 ± 0.06 μMol). The variability of the brain metabolic response was related to the level of ischaemia, suggesting that suppression of metabolism was due to lack of glucose substrate delivery rather than oxygen availability.
我们使用微型宽带近红外光谱(NIRS)系统监测了两名健康有经验的志愿者(2 名男性,年龄分别为 34 岁和 37 岁)在载人离心机诱导的高+Gz 加速过程中脑氧合(氧合和脱氧血红蛋白 [HbO]、[HHb])和氧化细胞色素 c 氧化酶 ([oxCCO])浓度的变化。我们进行了一系列的+Gz 暴露,在出现视觉症状(周边视野丧失)时终止。记录了系统参数(即心率、血压和动脉饱和度),并计算了脑血容量变化([HbT] = [HbO] + [HHb])和氧输送([HbDiff] = [HbO] - [HHb])。志愿者 1 的 [HbT] 下降了 -3.49 ± 0.02 μMol,[HbDiff] 下降了 -3.23 ± 0.44 μMol,[oxCCO] 增加了 0.42 ± 0.01 μMol。志愿者 2 的 [HbDiff] 下降了 -4.37 ± 0.23 μMol,[HbT](0.53 ± 0.06 μMol)和 [oxCCO](0.09 ± 0.06 μMol)没有显著变化。脑代谢反应的可变性与缺血程度有关,这表明代谢抑制是由于缺乏葡萄糖底物输送而不是氧气供应不足所致。