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. Author manuscript; available in PMC: 2024 Jul 1.
Published in final edited form as: J Mol Cell Cardiol. 2023 Apr 18;180:1–9. doi: 10.1016/j.yjmcc.2023.04.005

Table 1. Intracellular Ca2+ measurements in intact atrial myocytes.

Ca2+ handling parameters of Fura-2 acetoxymethyl-ester loaded atrial myocytes paced at 3 Hz followed by caffeine (10 mM) application. n=45 cells for +/+ vehicle, 44 cells for +/+ ent-verticilide, 33 cells for +/− vehicle, and 45 cells for +/− ent-verticilide. All data displayed as mean ± SD and analyzed using ANOVA multiple comparisons with Bonferroni-adjusted P values. CaT – pacing-induced Ca2+ transient, Caff.T – caffeine-induced Ca2+ transient

(A) Pitx2+/+ vehicle (n=45) (B) Pitx2+/+ ent-vert (n=44) (C) Pitx2+/− vehicle (n=33) (D) Pitx2+/− ent-vert (n=45) P values
(A) vs (B) (A) vs (C) (C) vs (D)
Diastolic Ca2+ (FRatio) 0.60 ± 0.07 0.56 ± 0.06 0.60 ± 0.09 0.59 ± 0.05 0.10 >0.99 >0.99
Time to peak (ms) 30.79 ± 5.04 29.45 ± 3.07 29.17 ± 3.03 29.36 ± 4.12 0.78 0.54 >0.99
CaT decay rate constant (ms) 114.2 ± 23.0 123.6 ± 24.6 114.1 ± 14.7 114.9 ± 18.8 0.24 >0.99 >0.99
SR Ca2+ content (FRatio) 0.83 ± 0.17 0.78 ± 0.16 0.91 ± 0.15 0.86 ± 0.09 0.89 0.10 >0.99
Caff.T decay rate constant (s) 2.95 ± 0.27 2.85 ± 0.38 2.85 ± 0.32 2.99 ± 0.32 >0.99 >0.99 0.53