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. 2022 Oct 27;12:18116. doi: 10.1038/s41598-022-21425-8

Figure 7.

Figure 7

Calcium dynamics in isolated intact FDB myofibers at room temperature. (A) Normalized traces (0–100%) of an ensemble average of FURA-2 calcium fluorescence (red) and sarcomere length (black) dynamics showing that the calcium transient time to peak precedes the peak of the sarcomere length transient. Inset shows same data and serves to highlight the differences of the peak timing (y-axis represents a 50% change from baseline, x-axis represents 0.10 s). (B) Summary statistics for time to peak for the calcium transient and sarcomere length changes shows peak amplitude of the calcium transient occurs significantly before the peak sarcomere length change (n = 13 myofibers in each group from n = 3 animals). (C) Summary statistics for the time to 50% of peak for the calcium transient and sarcomere length demonstrates there is a significant difference between the calcium kinetics (0.0037 ± 0.0005 s) and sarcomere length changes (0.0155 ± 0.0018 s) (n = 13 myofibers in each group from n = 3 animals). (D) Summary statistics for the time to 50% of baseline for the calcium transient (0.0508 ± 0.0087 s) and sarcomere length changes (0.0440 ± 0.0056 s) shows there is no significant difference in the recovery dynamics of calcium and sarcomere length relaxation (Sarcomere length: n = 13, FURA-2: n = 12 from n = 3 animals). Myofibers measured at room temperature with 0.2 Hz stimulation. Mean ± S.E.M. are presented, *P < 0.05.