Warman E N, Chiel H J
Department of Biology, Case Western Reserve University, Cleveland, OH 44106, USA.
J Neurosci Methods. 1995 Apr;57(2):161-9. doi: 10.1016/0165-0270(94)00144-6.
Using extracellular pipette electrodes made of glass or plastic whose tip diameters ranged from 60 to 100 microns, it was possible to record the activity of single identified neurons in freely behaving animals. Multiple pipettes can be reliably positioned and attached to the sheath. Large signals can be obtained from neurons having soma diameters as small as 70 microns. We have used this technique to monitor the activity of an identified interneuron (B4/B5) during feeding behavior in the marine mollusk Aplysia californica. The technique can also be used in reduced or in vitro preparations for rapidly mapping the neural activity of a ganglion without removing its sheath.
使用由玻璃或塑料制成、尖端直径在60至100微米之间的细胞外移液管电极,能够记录自由活动动物中单个已识别神经元的活动。多个移液管可以可靠地定位并连接到鞘上。对于胞体直径小至70微米的神经元也能获得大信号。我们已使用该技术监测海生软体动物加州海兔进食行为期间一个已识别中间神经元(B4/B5)的活动。该技术也可用于简化或体外制备,以便在不去除神经节鞘的情况下快速绘制其神经活动图谱。