Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, 4058 Basel, Switzerland.
STAR Protoc. 2021 Feb 17;2(1):100347. doi: 10.1016/j.xpro.2021.100347. eCollection 2021 Mar 19.
This protocol describes stable recordings of neuronal membrane potential in awake behaving, head-fixed mice. Previous protocols often highlight the need to minimize animal movements by anesthesia or restraint. This protocol is optimized to minimize brain movements during animal motion and has been used to record neurons in the olfactory bulb and visual cortex during active licking and locomotion behaviors. Under optimal conditions, success rates lie between 30% and 50% (recordings per microelectrode), with durations of up to 30 min. For complete details on the use and execution of this protocol, please refer to Jordan et al. (2018) and Jordan and Keller (2020).
本方案描述了在清醒活动、头部固定的小鼠中记录神经元膜电位的稳定记录。以前的方案经常强调需要通过麻醉或束缚来最小化动物的运动。本方案旨在最大限度地减少动物运动期间的大脑运动,并已用于在主动舔舐和运动行为期间记录嗅球和视觉皮层中的神经元。在最佳条件下,成功率介于 30%和 50%(每个微电极的记录)之间,持续时间长达 30 分钟。有关此方案使用和执行的完整详细信息,请参阅 Jordan 等人(2018 年)和 Jordan 和 Keller(2020 年)。