Inagaki Keiichiro, Heiney Shane A, Blazquez Pablo M
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Neurosci Methods. 2009 Apr 15;178(2):255-62. doi: 10.1016/j.jneumeth.2008.12.009. Epub 2008 Dec 14.
Microiontophoresis of neuroactive substances during single unit recording in awake behaving animals can significantly advance our understanding of neural circuit function. Here, we present a detailed description of a method for constructing carbon fiber multibarrel electrodes suitable for delivering drugs while simultaneously recording single unit activity from deep structures, including brainstem nuclei and the cerebellum, in the awake behaving primate. We provide data that should aid in minimizing barrel resistance and the time required to fill long, thin multibarrel electrodes with solutions. We also show successful single unit recording from a variety of areas in the awake squirrel monkey central nervous system, including the vestibular nuclei, Interstitial Nucleus of Cajal, and the cerebellum. Our descriptions and data should be useful for investigators wishing to perform single unit recordings during microiontophoresis of neuroactive substances, particularly in deep structures of animals with chronically implanted recording chambers.
在清醒行为动物的单神经元记录过程中,对神经活性物质进行微量离子电泳可显著促进我们对神经回路功能的理解。在此,我们详细描述一种构建碳纤维多管电极的方法,该电极适用于在清醒行为的灵长类动物中给药的同时,记录来自深部结构(包括脑干核团和小脑)的单神经元活动。我们提供的数据应有助于将电极管电阻以及用溶液填充细长多管电极所需的时间降至最低。我们还展示了在清醒松鼠猴中枢神经系统的多个区域成功进行单神经元记录的情况,这些区域包括前庭核、 Cajal间质核和小脑。我们的描述和数据对于希望在神经活性物质微量离子电泳过程中进行单神经元记录的研究人员应是有用的,特别是在具有长期植入记录腔的动物的深部结构中。