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. Author manuscript; available in PMC: 2012 Jun 26.
Published in final edited form as: Neuron. 2011 Jun 23;70(6):1143–1154. doi: 10.1016/j.neuron.2011.04.024

Figure 4.

Figure 4

Resting potentials and membrane time constants (τm) in gerbil OHCs. (A) Voltage responses to current steps in an apical OHC with the hair bundle exposed to 1.3 mM Ca2+, 0.02 mM Ca2+ and 0.2 mM DHS + 1.3 mM Ca2+. Note low Ca2+ depolarizes the OHC and reduces τm. Blocking MT channels with DHS hyperpolarizes the OHC and increases τm. τm was obtained by fitting voltage onsets (dashed lines) with: V = A(1 − exp (−t/τm)), where τm = 2.3 ms (1.3 Ca2+), 0.6 ms (0.02 Ca2+), 5.3 ms (1.3 Ca2+ + DHS). (B) Collected resting potentials (mean ± SEM) from apical OHCs with bundles exposed to 1.3 mM Ca2+ (control, n = 15; wash, n = 14), 0.02 mM Ca2+ (n= 5) and 0.2 mM DHS + 1.3 mM or 0.02 mM Ca2+ (n = 9). (C) Collected corner frequencies (F0.5 = 1/2πτm; mean ± SEM) calculated from τm measurements as in (A), numbers of measurements in each category as in (B). (D) Voltage responses to current steps with hair bundles perfused with 0.02 mM Ca2+ for three gerbil cochlear locations with different CFs. τm obtained from fits (dashed lines) and CF were: 0.67 ms (0.35 kHz); 0.23 ms (0.9 kHz); 0.10 ms (2.5 kHz).