Chen-Bee Cynthia H, Agoncillo Teodora, Xiong Ying, Frostig Ron D
Department of Neurobiology and Behavior, and the Center for the Neurobiology of Learning and Memory, University of California, Irvine, California 92697-4550, USA.
J Neurosci. 2007 Apr 25;27(17):4572-86. doi: 10.1523/JNEUROSCI.0326-07.2007.
Intrinsic signal optical imaging with red illumination (ISOI) is used extensively to provide high spatial resolution maps of stimulus-evoked hemodynamic-related signals as an indirect means to map evoked neuronal activity. This evoked signal is generally described as beginning with an undershoot or "dip" in signal that is faster, more transient, and weaker compared with the subsequent signal overshoot. In contrast, the evoked signal detected with blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) is generally described as containing an undershoot after the initial dip and overshoot, even though it, too, detects hemodynamic-related signals and its first two phases appear complementary to those of ISOI. Here, we used ISOI with 635 nm illumination to image over 13.5 s after a 1 s stimulus delivery to detect and successfully use the ISOI undershoot phase for functional mapping. Eight spatiotemporal attributes were assessed per signal phase including maximum areal extent and peak magnitude, both of which were largest for the ISOI overshoot, followed by the undershoot and then the initial dip. Peak activity location did not colocalize well between the three phases; furthermore, we found mostly modest correlations between attributes within each phase and sparse correlations between phases. Extended (13.5 s) electrophysiology recordings did not exhibit a reoccurrence of evoked suprathreshold or subthreshold neuronal responses that could be associated with the undershoot. Beyond the undershoot, additional overshoot/undershoot fluctuations were also mapped, but were typically less spatiotemporally specific to stimulus delivery. Implications for ISOI and BOLD fMRI are discussed.
红色照明下的内在信号光学成像(ISOI)被广泛用于提供刺激诱发的血流动力学相关信号的高空间分辨率图谱,作为映射诱发神经元活动的间接手段。这种诱发信号通常被描述为始于信号的下冲或“凹陷”,与随后的信号过冲相比,其速度更快、更短暂且更弱。相比之下,血氧水平依赖(BOLD)功能磁共振成像(fMRI)检测到的诱发信号通常被描述为在初始凹陷和过冲之后包含一个下冲,尽管它也检测血流动力学相关信号,并且其前两个阶段似乎与ISOI的互补。在这里,我们使用635 nm照明的ISOI在1秒刺激传递后对超过13.5秒进行成像,以检测并成功将ISOI下冲阶段用于功能映射。每个信号阶段评估了八个时空属性,包括最大面积范围和峰值幅度,这两个属性在ISOI过冲时最大,其次是下冲,然后是初始凹陷。三个阶段之间的峰值活动位置没有很好地共定位;此外,我们发现每个阶段内的属性之间大多具有适度的相关性,而阶段之间的相关性则很稀疏。延长(13.5秒)的电生理记录未显示出与下冲相关的诱发阈上或阈下神经元反应的再次出现。除了下冲之外,还映射了额外的过冲/下冲波动,但通常在时空上对刺激传递的特异性较低。讨论了对ISOI和BOLD fMRI的影响。