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. 2022 Mar 25;11(7):1114. doi: 10.3390/cells11071114

Figure 1.

Figure 1

L-type Ca2+ channels inhibition completely reversed the ISO-induced acceleration of depolarization rate in both dormant and spontaneously firing SANC isolated from WT mice. (A) Proportion of dormant and spontaneously firing SANC at baseline. (B) Current-clamp recording sample of dormant SANC initiating firing when injected with hyperpolarizing current. Average depolarization rates and illustrative examples of dormant ((CE), n = 8) and firing ((DF), n = 10) SANC at baseline and after perfusion of isoprenaline (ISO 100 nM) and subsequent perfusion of nifedipine (3 µM). * p < 0.05, ** p < 0.01, **** p < 0.0001 by parametric one-way ANOVA or non-parametric Friedman test.