Martin Chris, Jones Myles, Martindale John, Mayhew John
Centre for Signal Processing in Neuroimaging and Systems Neuroscience, Department of Psychology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Eur J Neurosci. 2006 Nov;24(9):2601-10. doi: 10.1111/j.1460-9568.2006.05135.x.
The relationship between localized changes in brain activity and metabolism, and the blood oxygenation level-dependent (BOLD) signal used in functional magnetic resonance imaging studies is not fully understood. One source of complexity is that stimulus-elicited changes in the BOLD signal arise both from changes in oxygen consumption due to increases in activity and purely 'haemodynamic' changes such as increases in cerebral blood flow. It is well established that robust cortical haemodynamic changes can be elicited by increasing the concentration of inspired CO(2) (inducing hypercapnia) and it is widely believed that these haemodynamic changes occur without significant effects upon neural activity or cortical metabolism. Hypercapnia is therefore commonly used as a calibration condition in functional magnetic resonance imaging studies to enable estimation of oxidative metabolism from subsequent stimulus-evoked functional magnetic resonance imaging BOLD signal changes. However, there is little research that has investigated in detail the effects of hypercapnia upon all components of the haemodynamic response (changes in cerebral blood flow, volume and oxygenation) in addition to recording neural activity. In awake animals, we used optical and electrophysiological techniques to measure cortical haemodynamic and field potential responses to hypercapnia (60 s, 5% CO(2)). The main findings are that firstly, in the awake rat, the temporal structure of the haemodynamic response to hypercapnia differs from that reported previously in anaesthetized preparations in that the response is more rapid. Secondly, there is evidence that hypercapnia alters ongoing neural activity in awake rats by inducing periods of cortical desynchronization and this may be associated with changes in oxidative metabolism.
大脑活动和代谢的局部变化与功能磁共振成像研究中使用的血氧水平依赖(BOLD)信号之间的关系尚未完全明了。复杂性的一个来源是,刺激引发的BOLD信号变化既源于活动增加导致的氧消耗变化,也源于纯粹的“血液动力学”变化,如脑血流量增加。众所周知,通过增加吸入的CO₂浓度(诱导高碳酸血症)可引发强烈的皮质血液动力学变化,并且人们普遍认为这些血液动力学变化对神经活动或皮质代谢没有显著影响。因此,高碳酸血症在功能磁共振成像研究中通常用作校准条件,以便根据随后刺激诱发的功能磁共振成像BOLD信号变化来估计氧化代谢。然而,除了记录神经活动外,很少有研究详细调查过高碳酸血症对血液动力学反应的所有组成部分(脑血流量、血容量和氧合的变化)的影响。在清醒动物中,我们使用光学和电生理技术来测量皮质对高碳酸血症(60秒,5% CO₂)的血液动力学和场电位反应。主要发现是,首先,在清醒大鼠中,对高碳酸血症的血液动力学反应的时间结构与之前在麻醉制剂中报道的不同,其反应更快。其次,有证据表明高碳酸血症通过诱导皮质去同步化时期改变清醒大鼠的持续神经活动,这可能与氧化代谢的变化有关。