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. 1997 Apr 1;17(7):2257–2266. doi: 10.1523/JNEUROSCI.17-07-02257.1997

Fig. 4.

Fig. 4.

Current–voltage relationship and voltage-jump relaxation kinetics for the H+-induced current.A, B, Voltage-clamp recordings from an rSERT-injected oocyte perfused with NMDG Ringer’s solution, pH 5.0, in the presence (A) or absence (B) of 10 μm desipramine. The membrane potential was held at −40 mV and then shifted for 600 msec to a series of test potentials ranging from −140 mV to +40 mV in 20 mV increments. C, Pure H+ leakage current obtained by subtracting Afrom B. Dashed line is at zero subtracted current. D, Steady-state currents obtained fromC were plotted as a function of membrane potential. Currents were averaged from the first 50 msec at the test potential.

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