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. Author manuscript; available in PMC: 2014 Dec 15.
Published in final edited form as: Cell Rep. 2014 May 15;7(5):1410–1416. doi: 10.1016/j.celrep.2014.04.039

Figure. 4. CDI of neuronal L-type Ca2+ channels is reduced by PKA pathway activation.

Figure. 4

(A) Internal perfusion with forskolin slows Ca2+-dependent inactivation of L-type current and increases current density. Peak Ca2+ current amplitude (red) was normalized to peak Ba2+ current (black) amplitude. Bar graphs present inactivation rates for Ca2+ and Ba2+ currents; number of individual cells recorded (n) is marked on each bar.

(B) Bath application of 100 μM cAMP analog (Sp-5,6-dichloro-cBIMPS) (bottom), but not 10 μM Sp-5,6-dichloro-cBIMPS (top), enhances current density and slows Ca2+-dependent inactivation. Error bars indicate standard error of the mean. Mean values were compared using ANOVA with a Bonferroni posthoc correction. Statistical significance marked as * p = 0.05, **** p = 0.001.