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. 2017 Jan 25;158(4):778–790. doi: 10.1210/en.2016-1702

Figure 2.

Figure 2.

P4 inhibits BPA-induced alterations of Ca2+ handling in female rat ventricular myocytes. (a) Representative images of Ca2+ sparks in quiescent myocytes under control, BPA, BPA + P4, or BPA + P4 + RU486 (1 μM). (b) Representative Ca2+ transients elicited by caffeine after field stimulation under various treatments. The amplitudes of caffeine-induced Ca2+ transients are indications of SR Ca2+ load. (c) Mean Ca2+ sparks frequency in myocytes under various treatments (n = 7 to 9 myocytes from four hearts). (d) Caffeine-induced Ca2+ transients amplitude (CaTcaff) in myocytes under various treatments (n = 8 to 10 myocytes from four hearts). BPA and P4 at 1 nM for all experiments. **P < 0.01; #P > 0.1 versus control; P < 0.01 (one-way analysis of variance). Error bars are standard error of the mean.