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. 2017 Aug 4;313(5):H1031–H1043. doi: 10.1152/ajpheart.00249.2017

Table 2.

Changes in cardiomyocyte Ca2+ handling in ovariectomized animal models

OVx Animal Guinea Pig (This Study) Rat Mouse
Peak L-type Ca2+ current A↑ (25) ↑ (18) and ↔ (17)
L-type Ca2+ channel mRNA↔ WB↑ (11) WB↓ (18)
mRNA↔ (11)
PKA E↑ (26)
A↑ (25)
CaMKIIδ and phosphorylated CaMKII WB↑ (30)
Sarcoplasmic reticulum Ca2+ content ↑ (17, 18)
Ca2+ transient amplitude ↑ (12, 25, 26) and ↓ (9) ↑ (17, 18) and ↓ (61)
Ca2+ transient time to peak ↓ (18)
Ca2+ transient rate constant ↑ (12, 26) ↑ (17, 18) and ↓ (61)
Fractional sarcoplasmic reticulum Ca2+ release ↔ (17, 18)
SERCA R↔ A↔ (26) and ↓ (8) WB↔ (18) and ↓ (61)
WB↔ (11, 26) and ↓ (7, 8)
mRNA↔ (11) and ↓ (8)
PLB↔ (7, 8, 11)
Na+/Ca2+ exchanger R↑ A↑ (26) WB↔ (18)
RC↑ (26)
WB↔ (26) and ↓ (11)
mRNA↔ (11)
Ryanodine receptor 2 A↑ (26)
WB↔ (11)
Spark frequency ↑ (17, 18)
Spark amplitude ↑ (17)
Spark mass ↑ (18) and ↔ (17)
Wave frequency
Isoprenaline-induced early afterdepolarizations and delayed afterdepolarizations

↑, increase compared with the sham group; ↔, no difference compared with the sham group; ↓, decrease compared with the sham group; A, activity; WB, Western blot; E, expression of fluorescence intensity; PLB, phospholamban; R, rate constant; RC, relaxation contribution.