Research Paper Volume 11, Issue 23 pp 11541—11564

Figure 8. Ca²⁺ transients in 1-mo old SGNs from WT and DKO mice. (A) Representative examples of line-scan images (inset) captured from unstimulated but spontaneous Ca²⁺ oscillations showing Ca²⁺ transients recorded from WT (upper panel, in black) and DKO (lower panel, in gray) SGNs. Sample records show SGN loaded with Fluo 4. (B) Summary data for the fast and slow time constant (τ₁ and τ₂) of the Ca²⁺ transient decay at baseline using two exponential functions. The τ₁ (ms) for WT = 48.4 ± 7.9; DKO = 73.2 ± 6.3; n = 19 (p = 0.019): and τ₂ (ms) for WT = 251.7 ± 24.5; DKO = 373.3 ± 44.2; n = 17 (p = 0.022). (C) Sample records show a region of interest (ROI) of ratiometric Fura 2 assessment of field potential (10V/4Hz) depolarization of WT and DKO SGN (arrows show the time of stimulation). Recovery after field stimulation had ~500-1000s time course (not shown). (D, E) Summary data for the amplitude of the total Ca²⁺ at baseline and after field stimulation in WT and DKO SGNs (1-mo old apical neurons). The F_340/380 for WT before field stimulation = 0.23 ± 0.01 (n = 28); DKO = 0.29 ± 0.03; n = 14 (p = 0.029): and after field stimulation WT = 0.29 ± 0.03 (n = 17); DKO = 0.46 ± 0.06; n = 11 (p = 0.007). Significant differences between genotypes were determined using unpaired two-tailed t-test.