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. 2015 Dec 29;10(12):e0144309. doi: 10.1371/journal.pone.0144309

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© 2015 Zhang et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 6 — (A) representative line scan image of Ca²⁺ release triggered by caffeine (10 mM). Example is from a Sham myocyte. Time scale as shown in B. (B) time course of changes in spatially averaged [Ca²⁺]_i of the cell shown in A. Horizontal and vertical lines axes indicate [Ca²⁺]_i and time scale, respectively. (C) Mean (±SEM) peak F/F₀ in the presence of caffeine in Sham (n/N = 10/5) and AoB (n/N = 13/6) cells. *, P<0.05, unpaired t-test.