Corfield Douglas R, McKay Leanne C
Manchester Medical School, University of Manchester, Manchester, UK.
Neuroscience and Molecular Pharmacology, Faculty of Biomedical and Life Sciences, University of Glasgow, Glasgow, UK.
Adv Exp Med Biol. 2016;903:157-67. doi: 10.1007/978-1-4899-7678-9_11.
A limited number of studies using differing imaging approaches suggest that there are regional variation in the cerebrovascular response to hypercapnia and hypoxia. However there are limitations to these studies. In particular, it is not clear if existing studies of hypoxia have fully accounted for the confounding effects of the changes in arterial PCO2 on cerebral perfusion that, if uncontrolled, will accompany the hypoxic stimulus. We determined quantitative maps of grey matter cerebral blood flow using a multi-slice pulsed arterial spin labelling MRI method at 3 T at rest, during conditions of isocapnic euoxia, hypercapnia, and mild isocapnic hypoxia. From these data, we determined grey matter cerebrovascular reactivity maps which show the spatial distribution of the responses to these interventions. Whilst, overall, cerebral perfusion increased with hypercapnia and hypoxia, hypoxia cerebrovascular reactivity maps showed very high variation both within and between individuals: most grey matter regions exhibiting a positive cerebrovascular reactivity, but some exhibiting a negative reactivity. The physiological explanation for this variation remains unclear and it is not known if these local differences will vary with state or with regional brain activity. The potential interaction between hypoxic or hypercapnic cerebrovascular changes and neurally related changes in brain perfusion is of particular interest for functional imaging studies of brain activation in which arterial blood gases are altered. We have determined the interaction between global hypoxia and hypercapnia-induced blood oxygen level-dependent (BOLD) MRI signal and local neurally related BOLD signal. Although statistically significant interactions were present, physiologically the effects were weak and, in practice, they did not change the statistical outcome related to the analysis of the neurally related signals. These data suggest that such respiratory-related confounds can be successfully accounted for in functional imaging studies.
少数采用不同成像方法的研究表明,脑血管对高碳酸血症和低氧血症的反应存在区域差异。然而,这些研究存在局限性。特别是,目前关于低氧血症的研究是否充分考虑了动脉血二氧化碳分压变化对脑灌注的混杂影响尚不清楚,若不加以控制,这种影响将伴随低氧刺激出现。我们使用多切片脉冲动脉自旋标记磁共振成像方法,在3T静息状态下、等碳酸正常氧、高碳酸血症和轻度等碳酸低氧条件下,测定了灰质脑血流量的定量图谱。根据这些数据,我们确定了灰质脑血管反应性图谱,该图谱显示了对这些干预措施反应的空间分布。总体而言,随着高碳酸血症和低氧血症的出现,脑灌注增加,但低氧血症脑血管反应性图谱在个体内部和个体之间均显示出很大差异:大多数灰质区域表现出正的脑血管反应性,但有些区域表现出负的反应性。这种差异的生理学解释仍不清楚,也不知道这些局部差异是否会随状态或区域脑活动而变化。低氧或高碳酸脑血管变化与脑灌注中神经相关变化之间的潜在相互作用,对于动脉血气发生改变的脑激活功能成像研究尤为重要。我们已经确定了全身性低氧血症和高碳酸血症诱导的血氧水平依赖(BOLD)磁共振成像信号与局部神经相关BOLD信号之间的相互作用。尽管存在统计学上的显著相互作用,但从生理学角度来看,这些影响很微弱,实际上,它们并没有改变与神经相关信号分析相关的统计结果。这些数据表明,在功能成像研究中,可以成功地考虑到这种与呼吸相关的混杂因素。