Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2017 Nov 14;4(6):ENEURO.0303-17.2017. doi: 10.1523/ENEURO.0303-17.2017

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2017 Browne et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

PMC Copyright notice

Figure 5. — Persistent and resurgent Na⁺ currents have an increased prevalence by hearing onset. A, Representative Na⁺ currents elicited in basal and apical SGNs, at developmental stages before (P6) and after the onset of hearing (P14, P21, P80). TTX-sensitive difference currents were elicited using the voltage protocol in Figure 3A. B, Scatter plot of I_NaR/I_NaT ratios for individual SGNs at various developmental ages. C, Variations in I_NaR/I_NaT at different tonotopic locations. Individual data from B has been grouped (P0-P1, P3, P5, P6, P8, P12-P14, P21, and P80-P90) and separated into tonotopic origin (base, mid, and apex). D, Mean I_NaR/I_NaT ratio for all SGNs (basal and apical cells pooled) plotted as a function of test potentials at various developmental ages (P6, n = 9; P12-P14, n = 30; P80-P90, n = 12). E, Mean I_NaP/I_NaT ratio plotted as a function of test potentials, for the same cells as in D.