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. Author manuscript; available in PMC: 2009 Mar 11.
Published in final edited form as: Am J Physiol Cell Physiol. 2006 Oct 25;292(3):C1156–C1166. doi: 10.1152/ajpcell.00397.2006

Fig. 6.

Fig. 6

Frequency of Ca2+ events in dedifferentiated adult FDB fibers decreases with addition of Ca2+ channel blockers. All fibers were cultured for 6–7 days in CoCl2-free, nifedipine-free, serum-containing medium before each experiment. A: fibers cultured in serum-containing media were bathed in Ringer solution and imaged both before and after the addition of 5 mM CoCl2 as indicated. B: time course of resting fiber fluorescence in the same fibers both before and after the addition of CoCl2. C: fibers cultured in serum-containing media were bathed in Ringer solution and imaged both before and after the addition of 5 μM nifedipine as indicated. D: time course of resting fiber fluorescence in the same fibers both before and after the addition of nifedipine. E: fibers cultured in serum-containing media were bathed in Ringer solution and imaged for spark activity without Ca2+ channel blocker treatment. F: time course of resting fiber fluorescence in the same fibers without Ca2+ channel blocker treatment; n = 21 in A and B, n = 10 in C and D, and n = 10 in E and F. Statistical significance was determined using a 1-way ANOVA test (P < 0.05). Groups with the same letter exhibit significant difference from each other.

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