神经影像学
神经科学
离体
钙显像
运动前神经元活动
荧光寿命成像显微镜
光学成像
体内
大脑活动与冥想
显微镜
大脑定位
临床前影像学
化学
功能成像
生物医学工程
生物
医学
荧光
钙
病理
脑电图
内科学
光学
物理
生物技术
作者
Sven Gottschalk,Oleksiy Degtyaruk,Benedict Mc Larney,Johannes Rebling,Magdalena Anastasia Hutter,Xosé Luís Deán‐Ben,Shy Shoham,Daniel Razansky
标识
DOI:10.1038/s41551-019-0372-9
摘要
Efforts to scale neuroimaging towards the direct visualization of mammalian brain-wide neuronal activity have faced major challenges. Although high-resolution optical imaging of the whole brain in small animals has been achieved ex vivo, the real-time and direct monitoring of large-scale neuronal activity remains difficult, owing to the performance gap between localized, largely invasive, optical microscopy of rapid, cellular-resolved neuronal activity and whole-brain macroscopy of slow haemodynamics and metabolism. Here, we demonstrate both ex vivo and non-invasive in vivo functional optoacoustic (OA) neuroimaging of mice expressing the genetically encoded calcium indicator GCaMP6f. The approach offers rapid, high-resolution three-dimensional snapshots of whole-brain neuronal activity maps using single OA excitations, and of stimulus-evoked slow haemodynamics and fast calcium activity in the presence of strong haemoglobin background absorption. By providing direct neuroimaging at depths and spatiotemporal resolutions superior to optical fluorescence imaging, functional OA neuroimaging bridges the gap between functional microscopy and whole-brain macroscopy.
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