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. 2019 Jul 10;1(1):84–102. doi: 10.1016/j.jaccao.2019.06.003

Table 1.

Echocardiographic Analyses in the Mouse Chronic Toxicity Model

Vehicle (n = 10) IS20 (n = 11) DOX (n = 13) DOX + IS20 (n = 17)
Heart rate (beats/min) 512 ± 19 506 ± 22 436 ± 11 457 ± 18
LA/BW (mm/g) 0.08 ± 0.01 0.08 ± 0.01 0.10 ± 0.02 0.09 ± 0.02
LVESD (mm) 2.60 ± 0.44 2.73 ± 0.31 2.99 ± 0.52 2.85 ± 0.4
LVEDD (mm) 4.19 ± 0.31 4.08 ± 0.24 4.1 ± 0.46 4.18 ± 0.40
LVEDe D/BW (mm/g) 0.14 ± 0.01 0.13 ± 0.01 0.18 ± 0.02 0.18 ± 0.02
LV systolic function
 EF (%) 75 ± 16 71 ± 6 65 ± 9 69.5 ± 3.7
 Sa (cm/s) 2.72 ± 0.8 2.33 ± 0.8 1.77 ± 0.7 2.03 ± 0.6
 Spw (cm/s) 2.67 ± 0.4 2.52 ± 0.4 2.08 ± 0.6 2.16 ± 0.5
LV diastolic function
 E′a (cm/s) 3.8 ± 1.2 3.28 ± 1 2.46 ± 0.8 2.68 ± 1
 E′pw (cm/s) 3.5 ± 1 3.1 ± 0.7 2.3 ± 0.7 3.0 ± 1 t

Values are mean ± SD.

BW = body weight; DOX = doxorubicin; E′a = diastolic velocity of mitral annulus; E′pw = diastolic velocity of posterior wall; EF = ejection fraction; IVRT = isovolumic relaxation time; LA = left atrium; LVEDD = left ventricular end-diastolic diameter; LVESD = left ventricular end-systolic diameter; Sa = systolic velocity of mitral annulus; Spw = systolic velocity of posterior wall.

p < 0.05 vs. vehicle.

p < 0.05 vs. doxorubicin (DOX).