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. 2018 Oct 25;22(6):697–703. doi: 10.4196/kjpp.2018.22.6.697

Fig. 3. Downregulation of inward-rectifying K+ channel in ρ0 myoblasts.

Fig. 3

(A) Representative chart trace recordings of inward-rectifying K+ current (IKir) in symmetrical KCl solution. For whole-cell patch-clamp recordings, the current was obtained by step depolarizing pulse ranging from −140 mV to 70 mV at a holding potential of 0 mV. (B) Average I–V relationship curve for the peak IKir from −140 to 70 mV between control (n=13) and ρ0 myoblasts (n=13). *p<0.05. (C) Immunoblot assay of KIR2.1 and β-actin expression in control and ρ0 myoblasts. KIR2.1 signals were normalized to the β-actin signal, and mean values are displayed as bar graphs (n=3). *p<0.05. Data are means±standard error of the mean. (D) Average I–V relationship curve of IKir following treatment with antimycin A (n=7) and in control myoblasts (n=7) in normal myocytes. (E) Current density of IKir at −120 mV. **p<0.01. All data are presented as the mean±standard error of the mean.