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Large-scale recording of thalamocortical circuits: in vivo electrophysiology with the two-dimensional electronic depth control silicon probe.

机译:丘脑皮质回路的大规模记录:带有二维电子深度控制硅探针的体内电生理学。

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摘要

Recording simultaneous activity of a large number of neurons in distributed neuronal networks is crucial to understand higher order brain functions. Here, we demonstrate the in vivo performance of a recently developed electrophysiological recording system comprising a two-dimensional, multi-shank, high-density silicon probe with integrated CMOS electronics. The system implements the concept of electronic depth control (EDC), which enables the electronic selection of a limited number of recording sites on each of the probe shafts. This innovative feature of the system permits simultaneous recording of local field potentials (LFP), and single- and multiple-unit activities (SUA and MUA, respectively) from multiple brain sites with high quality and without the actual physical movement of the probe. To evaluate the in vivo recording capabilities of the EDC probe, we recorded LFP, MUA and SUA in acute experiments from cortical and thalamic brain areas of anesthetized rats and mice. The advantages of large-scale recording with the EDC probe are illustrated by investigating the spatiotemporal dynamics of pharmacologically induced thalamocortical slow wave activity in rats, by comparing the firing and burst properties of neurons located in various thalamic nuclei and by the two-dimensional tonotopic mapping of the auditory thalamus. In mice, spatial distribution of thalamic responses to optogenetic stimulation of the neocortex was examined. Utilizing the benefits of the EDC system may result in a higher yield of useful data from a single experiment compared to traditional passive multielectrode arrays, and thus in the reduction of animals needed for a research study.
机译:在分布式神经元网络中记录大量神经元的同时活动对于理解高级脑功能至关重要。在这里,我们演示了最近开发的电生理记录系统的体内性能,该系统包括带有集成CMOS电子器件的二维,多柄,高密度硅探针。该系统实现了电子深度控制(EDC)的概念,该概念使电子选择每个探针杆上有限数量的记录位置成为可能。该系统的创新功能允许同时记录来自多个大脑部位的局部场电势(LFP),以及来自多个大脑部位的单单元和多单元活动(分别为SUA和MUA),而无需进行探针的实际物理运动。为了评估EDC探针的体内记录能力,我们在急性实验中从麻醉的大鼠和小鼠的皮质和丘脑区域记录了LFP,MUA和SUA。通过研究大鼠药理学诱发的丘脑皮层慢波活动的时空动态,比较位于各个丘脑核中的神经元的放电和爆发特性以及通过二维层析成像,证明了使用EDC探针进行大规模记录的优势。听丘脑。在小鼠中,检查了丘脑对新皮层的光遗传学刺激的反应的空间分布。与传统的无源多电极阵列相比,利用EDC系统的好处可以从单个实验中获得更高的有用数据产量,从而减少了研究所需的动物数量。

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