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. 2014 May 27;9(5):e98277. doi: 10.1371/journal.pone.0098277

Figure 6. VE and LOC neurons express transient outward currents.

Figure 6

Isolations of sustained and inactivating outward currents under influence of 0.5 µM TTX and 500 µM TEA in voltage clamped VE neurons (A–D). Two voltage clamp protocols, depolarizing the neuron in 10 mV, 500 ms, steps from a holding potential of −60 mV up to +10 mV (a), were used to trigger sustained outward currents (A). In one protocol the depolarization was preceded by a −100 mV, 50 ms hyperpolarization step to de-inactivate potential low-voltage activated currents (b). This protocol, in addition to the sustained currents, triggered large inactivating currents (B) The inactivating current component (C) was then isolated by subtracting the currents elicited in the first protocol (a) from those in the second protocol (b). The same protocols and pharmacological substances were used to isolate the transient outward current in LOC neurons (D). The insets display the identification of the neuron types in current clamp mode prior to application of the drugs. Averages of the peak transient outward currents recorded in VE (open squares, n = 6) and LOC (filled circles, n = 10) are plotted against the voltage, revealing larger currents in the VE than the LOC neurons (E). When normalizing the peak current values to the compensated capacitance for each neuron, thus obtaining the current densities, the LOC neurons express larger transient outward currents than the VE neurons throughout the voltage range tested (F). Steady state activation and inactivation curves were generated by normalizing the mean current at each voltage for the respective VE (G) and LOC (H) neurons and fitting Boltzmann functions to the data. The inactivation currents were recorded at voltages of −10 mV, which was preceded by 1.5 second voltage steps ranging from −110 to −40 mV.