Battaglia Francesco P, Kalenscher Tobias, Cabral Henrique, Winkel Jasper, Bos Jeroen, Manuputy Ron, van Lieshout Theo, Pinkse Frans, Beukers Harry, Pennartz Cyriel
Center for Neuroscience, Swammerdam Institute for Life Sciences, Faculty of Science, Universiteit van Amsterdam, Amsterdam, The Netherlands.
J Neurosci Methods. 2009 Apr 15;178(2):291-300. doi: 10.1016/j.jneumeth.2008.12.024. Epub 2008 Dec 30.
In vivo electrophysiological recordings from groups of distinguishable neurons in behaving mice is a technique with a rapidly growing appeal, particularly because it can be combined with gene targeting techniques. This methodology is deemed essential for achieving a flexible and versatile coupling of molecular-genetic manipulations with behavioral and system level analyses of the nervous system. One major obstacle in obtaining this technological integration is the relatively high weight and bulk size of the available implantable devices for ensemble recordings as compared to the size of the animal. This imposes considerable physical stress on the animals and may prevent them from performing complex behavioral tasks for more than a few minutes. We developed a novel micro-drive which allows independent day-to-day positioning of up to 6 tetrodes in the mouse brain, with an extremely reduced weight and size. The system is based on an "exoskeleton" as its structural element, and allows a completely rectilinear path of the electrodes inside the drive and into the brain. Tests showed that mice can tolerate the chronically implanted device very well up to 12 weeks after implantation, while exhibiting normal behavior. Cell yields and stability obtained with this drive in two different brain areas (the hippocampus and orbitofrontal cortex) were comparable to those of traditional recording systems, usually applied to rats. The device may greatly expand possibilities to combine gene targeting and ensemble recording techniques, in behaviorally varied as well as cognitively demanding settings.
对行为小鼠体内可区分神经元群体进行电生理记录是一种吸引力迅速增长的技术,特别是因为它可以与基因靶向技术相结合。这种方法被认为是实现分子遗传操作与神经系统行为和系统水平分析灵活通用耦合的关键。获得这种技术整合的一个主要障碍是,与动物大小相比,用于群体记录的现有可植入设备重量和体积相对较大。这给动物带来了相当大的身体压力,可能会使它们无法进行超过几分钟的复杂行为任务。我们开发了一种新型微驱动器,它允许在小鼠大脑中独立地逐日定位多达6根四极管,其重量和尺寸极大地减小。该系统基于“外骨骼”作为其结构元件,并允许电极在驱动器内部以及进入大脑时完全直线运动。测试表明,小鼠在植入后长达12周的时间里能够很好地耐受长期植入的设备,同时表现出正常行为。在两个不同脑区(海马体和眶额皮质)使用该驱动器获得的细胞产量和稳定性与通常应用于大鼠的传统记录系统相当。该设备可能会极大地扩展在行为多样以及认知要求较高的环境中结合基因靶向和群体记录技术的可能性。