Table 1.
Mdx mouse groups: | Vehicle (n = 10) | Nicorandil (n = 10) | Isoproterenol (n = 14) | Nicorandil + Isoproterenol (n = 14) |
---|---|---|---|---|
Baseline characteristics | ||||
Age at study end (weeks) | 13.0 ± 0.52 | 13.4 ± 0.44 | 13.4 ± 0.47 | 13.4 ± 0.51 |
Body weight at study end (g) | 25.8 ± 0.53 | 26.2 ± 0.45 | 26.4 ± 0.46 | 25.1 ± 0.45 |
Echocardiographic measurements | ||||
Heart rate (beats per minute) | ||||
Baseline | 419 ± 16 | 472 ± 16 | 394 ± 19 | 451 ± 14 |
Day 10 | 501 ± 11* | 485 ± 14 | 454 ± 14* | 489 ± 13* |
Ejection fraction (%) | ||||
Baseline | 71.3 ± 1.8 | 75.9 ± 2.1 | 75.2 ± 1.6 | 75.9 ± 1.6 |
Day 10 | 71.9 ± 2.3 | 72.6 ± 2.5 | 68.1 ± 2.6* | 74.8 ± 1.6 |
Fractional shortening (%) | ||||
Baseline | 35.3 ± 1.5 | 39.2 ± 1.8 | 38.6 ± 1.3 | 39.2 ± 1.4 |
Day 10 | 36.0 ± 1.8 | 36.6 ± 2.0 | 33.4 ± 1.9* | 38.2 ± 1.5 |
Left ventricular end systolic volume (mL) | ||||
Baseline | 0.030 ± 0.003 | 0.027 ± 0.004 | 0.028 ± 0.003 | 0.025 ± 0.003 |
Day 10 | 0.040 ± 0.007 | 0.040 ± 0.005 | 0.047 ± 0.005* | 0.030 ± 0.003* |
Left ventricular end diastolic volume (mL) | ||||
Baseline | 0.116 ± 0.008 | 0.190 ± 0.011 | 0.111 ± 0.005 | 0.099 ± 0.007 |
Day 10 | 0.119 ± 0.015 | 0.128 ± 0.011 | 0.144 ± 0.007* | 0.114 ± 0.009 |
Stroke volume (mL) | ||||
Baseline | 0.083 ± 0.006 | 0.080 ± 0.007 | 0.083 ± 0.003 | 0.074 ± 0.005 |
Day 10 | 0.083 ± 0.008 | 0.093 ± 0.008 | 0.096 ± 0.005* | 0.082 ± 0.007 |
Echocardiograms were performed at baseline and at 10 days. Isoproterenol induced left ventricular dilation and a mild cardiac injury with a decrease in ejection fraction and fractional shortening and an increased end systolic volume. Nicorandil was protective against left ventricular dilation and isoproterenol-induced injury. (*p < 0.05 vs same group baseline measurement)