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

Figure 8.

Figure 8

Calcium dynamics in isolated intact FDB myofibers at 37 °C. (A) Normalized traces (0–100%) of an ensemble average of FURA-2 calcium fluorescence (red) and sarcomere length (black) dynamics. Inset shows same data and serves to highlight the region of the peak amplitude (y-axis represents a 50% change from baseline, x-axis represents 0.10 s). (B) Summary statistics for time to peak of the calcium transient and sarcomere length changes shows timing of the peak calcium amplitude occurs significantly before the time to peak of the sarcomere length (Sarcomere length: n = 21, FURA n = 19 from n = 2 animals). (C) Summary statistics for the time to 50% of peak for the calcium transient and sarcomere length demonstrates that the calcium transient (0.0038 ± 0.0003 s) is significantly faster than the sarcomere length change (0.0084 ± 0.0006 s) (Sarcomere length: n = 21, FURA n = 19 from n = 2 animals). (D) Summary statistics for the time to 50% of baseline for the FURA-2 calcium transient and sarcomere length changes shows there is a significant difference in the recovery dynamics of the calcium transient and sarcomere length, with the calcium transient (0.0161 ± 0.0015 s) recovering more quickly than the relaxation of the myofiber (0.0228 ± 0.0018 s) (Sarcomere length: n = 21, FURA n = 19 from n = 2 animals). Myofibers measured at 37 °C with 0.2 Hz stimulation. Mean ± S.E.M. are presented, *P < 0.05.