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The differential pulse voltammograms were recorded by applying positive going potentials from 0.53 to 0.98 V.
Transepithelial resistance was recorded by applying a 10-mV pulse per second via an automated pulse generator.
EIS measurements were recorded by applying an AC voltage of 10 mV over a frequency range of 105 to 0.01 Hz.
The temperature variation of the strip was recorded by applying a constant current and monitoring the resistivity change with time from which the liquid thermal conductivity was deduced.
PPT was recorded by applying pressure on the most prominent point of the masseter muscle during contraction, and on the right index finger, which was used as an extra-cranial reference point.
Briefly, KCa currents were recorded by applying a 25 ms-depolarizing step to +30 mV from a holding potential of −40 mV in normal external saline and after 3 min incubation in Ca2+-free external saline.
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Intracellular contents were removed from the recorded neuron by applying negative pressure, via mouth pipetting or a manometer, to the recording pipet while simultaneously recording the neuron's physiology and visualizing the cell using Dodt contrast.
After completion of the recordings, Lucifer yellow was injected into the recorded cell by applying a hyperpolarizing current.
The impedance spectra were recorded potentiostatically by applying an AC voltage of 5-mV amplitude over a frequency range from 100 kHz to 5 mHz.
To isolate sEPSCs, the authors blocked inhibitory currents in the recorded neuron by applying a GABA-A receptor antagonist, picrotoxin, from the internal solution of the patch pipette (Akaike et al., 1985).
In these two papers, they preserve the privacy of records by applying Bloom filters.
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