Table 3.
Effect of istaroxime on the kinetic parameters for Ca2+ uptake into cardiac SR vesiscles from healthy dogs by a stopped-flow method
| Free Ca2+ 0.19 μM | k1 (s−1) | A1 | k2 (s−1) | A2 |
|---|---|---|---|---|
| Control N = 8 | 0.4117 ± 0.0379 | 0.003308 ± 0.00046 | 0.066 ± 0.0096 | 0.00474 ± 0.00022 |
| + Istar N = 8 | 0.5854 ± 0.0351* | 0.003483 ± 0.00023 | 0.0841 ± 0.0067* | 0.00376 ± 0.00012 |
| Free Ca2+ 2 μM | k1 (s−1) | A1 | k2 (s−1) | A2 |
|---|---|---|---|---|
| Control N = 8 | 0.5523 ± 0.0449 | 0.00282 ± 0.000158 | 0.0911 ± 0.0060 | 0.00357 ± 0.00019 |
| + Istar N = 8 | 0.7348 ± 0.0036* | 0.00341 ± 0.000258 | 0.1187 ± 0.0103* | 0.00407 ± 0.00017 |
Data are mean ± SEM of absorbance at 650 nm measured in the absence (control) and presence of 100 nM istaroxime at 0.19 and 2 μM free Ca2+ concentrations. N, number of replicates of time course experiments; k1, rate constant for fast phase of Ca2+ uptake; k2, rate constant for slow phase of Ca2+ uptake; A1, amplitude of fast phase of Ca2+ uptake; A2, amplitude of slow phase of Ca2+ uptake. The statistical significance between control and istaroxime was measured by t-test analysis.
P < 0.05 istaroxime versus control.