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. 2014 May 29;9(5):e97310. doi: 10.1371/journal.pone.0097310

Figure 6. Glial cell in cat visual cortex in vivo recorded with the TZS method.

Figure 6

(A–B) As in Figure 2, voltage and current recordings during the approach to the cell and subsequent whole-cell access. Here, an initial spontaneous seal with a subsequent “zap” was accomplished, but in distinction to the TZ endpoints illustrated in Figures 2, 3 and 5, the membrane resealed (between 24 and 27 seconds), and whole-cell access was re-established by suction at ∼46 seconds (not visible in (B)). (C) Voltage responses to current steps (100 nA increments from −200 to 700 nA). (D) Left – Preferred (270°) and non-preferred (0°) voltage responses (average of 10 trials) to a moving sinusoidal grating (4 Hz, 100% contrast, 5 second duration). Right – Average standard deviation of the visual responses (over the 10 trials) as a function of stimulus direction, showing that this cell is tuned to stimulus direction, with a small bias for stimulus orientation. The on-line corrected Ra was 40 MΩ, which was validated off-line. The input resistance was 99 MΩ, giving a relative Ra of 0.40.