Osanai Hisayuki, Kitamura Takashi, Yamamoto Jun
Department of Psychiatry, University of Texas Southwestern Medical Center.
Department of Psychiatry, University of Texas Southwestern Medical Center; Department of Neuroscience, University of Texas Southwestern Medical Center.
J Vis Exp. 2019 Aug 10(150). doi: 10.3791/60028.
Multi-regional neural recordings can provide crucial information to understanding fine-timescale interactions between multiple brain regions. However, conventional microdrive designs often only allow use of one type of electrode to record from single or multiple regions, limiting the yield of single-unit or depth profile recordings. It also often limits the ability to combine electrode recordings with optogenetic tools to target pathway and/or cell type specific activity. Presented here is a hybrid microdrive array for freely moving mice to optimize yield and a description of its fabrication and reuse of the microdrive array. The current design employs nine tetrodes and one opto-silicon probe implanted in two different brain areas simultaneously in freely moving mice. The tetrodes and the opto-silicon probe are independently adjustable along the dorsoventral axis in the brain to maximize the yield of unit and oscillatory activities. This microdrive array also incorporates a set-up for light, mediating optogenetic manipulation to investigate the regional- or cell type-specific responses and functions of long-range neural circuits. In addition, the opto-silicon probe can be safely recovered and reused after each experiment. Because the microdrive array consists of 3D-printed parts, the design of microdrives can be easily modified to accommodate various settings. First described is the design of the microdrive array and how to attach the optical fiber to a silicon probe for optogenetics experiments, followed by fabrication of the tetrode bundle and implantation of the array into a mouse brain. The recording of local field potentials and unit spiking combined with optogenetic stimulation also demonstrate feasibility of the microdrive array system in freely moving mice.
多区域神经记录可为理解多个脑区之间的精细时间尺度相互作用提供关键信息。然而,传统的微驱动器设计通常只允许使用一种类型的电极从单个或多个区域进行记录,这限制了单神经元或深度剖面记录的产量。它还常常限制了将电极记录与光遗传学工具相结合以靶向特定通路和/或细胞类型活动的能力。本文介绍了一种用于自由活动小鼠的混合微驱动器阵列,以优化产量,并描述了其制造和微驱动器阵列的重复使用。当前的设计采用九个四极管和一个光硅探针,同时植入自由活动小鼠的两个不同脑区。四极管和光硅探针可在脑中沿背腹轴独立调节,以最大限度地提高单位活动和振荡活动的产量。这种微驱动器阵列还集成了一个光装置,介导光遗传学操作,以研究长程神经回路的区域或细胞类型特异性反应和功能。此外,光硅探针在每次实验后都可以安全回收和重复使用。由于微驱动器阵列由3D打印部件组成,微驱动器的设计可以很容易地修改以适应各种设置。首先描述的是微驱动器阵列的设计以及如何将光纤连接到用于光遗传学实验的硅探针上,随后是四极管束的制造以及将阵列植入小鼠大脑。局部场电位和单位放电记录与光遗传学刺激相结合,也证明了微驱动器阵列系统在自由活动小鼠中的可行性。