The effect of hypercapnia on the neural and hemodynamic responses to somatosensory stimulation

被引:89
作者
Jones, M [1 ]
Berwick, J [1 ]
Hewson-Stoate, N [1 ]
Gias, C [1 ]
Mayhew, J [1 ]
机构
[1] Univ Sheffield, Dept Psychol, Ctr Signal Proc Neuroimaging & Syst Neurosci, Sheffield S10 2TP, S Yorkshire, England
关键词
hypercapnia; hemodynamic responses; deoxyhemoglobin; fMRI; optical imaging; barrel cortex;
D O I
10.1016/j.neuroimage.2005.04.036
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Modern non-invasive imaging techniques utilize the coupling between neural activity and changes in blood flow, volume and oxygenation to map the functional architecture of the human brain. An understanding of how the hemodynamic response is influenced by pre-stimulus baseline perfusion is important for the interpretation of imaging data. To address this issue, the present study measured hemodynamics with optical imaging spectroscopy and laser Doppler flowmetry, while multichannel electrophysiology was used to record local field potentials (LFP) and multi-unit activity (MUA). The response to whisker stimulation in rodent barrel cortex was recorded during baseline (normocapnia) and elevated perfusion rates produced by two levels of hypercapnia (5 and 10%). With the exception of the 'washout' of deoxyhemoglobin, which was attenuated, all aspects of the neural and hemodynamic response to whisker stimulation were similar during 5% hypercapnia to those evoked during normocapnia. In contrast, 10% hypercapnia produced cortical arousal and a reduction in both the current sink and MUA elicited by stimulation. Blood flow and volume responses were reduced by a similar magnitude to that observed in the current sink. The deoxyhemoglobin 'washout', however, was attenuated to a greater degree than could be expected from the neural activity. These data suggest that imaging techniques based on perfusion or blood volume changes may be more robust to shifts in baseline than those based on the dilution of deoxyhemoglobin, such as conventional BOLD fMRI. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:609 / 623
页数:15
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