DiCarlo J J, Lane J W, Hsiao S S, Johnson K O
Department of Neuroscience, Johns Hopkins University, Baltimore, MD 21218, USA.
J Neurosci Methods. 1996 Jan;64(1):75-81. doi: 10.1016/0165-0270(95)00113-1.
Fluorescent dyes were used to mark and identify the tracks left by extracellular microelectrodes in neurophysiological experiments. Forty-two penetrations were made into the postcentral gyrus of 3 Macaque monkeys with electrodes coated with 1 of 5 fluorescent dyes (DiI, DiO, DiI-C5, PyPO, and Fast Blue). The electrodes were driven at rates ranging from 10 to 1000 microns/min, to a depth of about 4000 microns, where a small electrolytic lesion was made. Histological sections were viewed under fluorescent optics and the electrode tracks were reconstructed from the dye traces. Fluorescent traces (width 50-400 microns) were observed in 41 of 42 penetrations with 24 traces extending to the lesion site. Of the electrodes driven in less than 3 h, those coated with DiI (8/8) and DiI-C5 (8/8) left a trace to the lesion site, while 57% (4/7) of the DiO, 40% (2/5) of the Fast Blue and only 11% (1/9) of the PyPO tracks were fully marked. This method of marking penetrations can be used with any extracellular recording configuration, does not require tissue sections to be processed or stained, does not require electrical lesions, and causes no detectable tissue damage. Because the dyes fluoresce at different wavelengths, closely spaced tracks can be uniquely identified.
在神经生理学实验中,荧光染料被用于标记和识别细胞外微电极留下的轨迹。用涂有5种荧光染料(DiI、DiO、DiI-C5、PyPO和固蓝)之一的电极对3只猕猴的中央后回进行了42次穿刺。电极推进速度为10至1000微米/分钟,推进深度约为4000微米,在该深度处进行了小的电解损伤。在荧光光学下观察组织切片,并根据染料痕迹重建电极轨迹。在42次穿刺中的41次观察到荧光痕迹(宽度50 - 400微米),其中24条痕迹延伸至损伤部位。在推进时间少于3小时的电极中,涂有DiI(8/8)和DiI-C5(8/8)的电极留下了延伸至损伤部位的痕迹,而DiO的57%(4/7)、固蓝的40%(2/5)以及PyPO轨迹中只有11%(1/9)被完全标记。这种标记穿刺轨迹的方法可用于任何细胞外记录配置,无需对组织切片进行处理或染色,无需电损伤,且不会造成可检测到的组织损伤。由于染料在不同波长下发出荧光,因此可以唯一地识别紧密间隔的轨迹。