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. 2009 Dec 11;298(3):H807–H815. doi: 10.1152/ajpheart.00877.2009

Table 1.

In vivo cardiac performance of WT and PLM-KO mice

WT PLM-KO
Echocardiography
    Body wt, g 25.3 ± 0.4 (5) 24.4 ± 0.4 (5)
    LVIDD, mm 3.27 ± 0.02 3.55 ± 0.06*
    LVIDS, mm 1.73 ± 0.13 2.03 ± 0.04
    ANT, mm 0.51 ± 0.00 0.60 ± 0.00*
    PWT, mm 0.54 ± 0.02 0.65 ± 0.01*
    LV mass, mg 38.5 ± 2.0 55.8 ± 1.1*
    Heart rate, beats/min 401 ± 18 406 ± 13
    Ejection fraction, % 78.9 ± 4.1 74.8 ± 1.2
    Fractional shortening, % 47.1 ± 3.7 42.8 ± 1.1
    Stroke volume, μl 34.2 ± 1.7 39.5 ± 1.8
    Cardiac output, ml/min 13.8 ± 1.0 16.0 ± 0.9
In vivo catheterization
    +dP/dt, mmHg/s 6,728 ± 304 (9) 7,920 ± 338* (14)
    Max +dP/dt, mmHg/s 13,559 ± 896 13,642 ± 363
    −dP/dt, mmHg/s 7,189 ± 341 8,163 ± 365
    Max −dP/dt, mmHg/s 13,903 ± 1278 11,750 ± 933*

Values are means ± SE for no. of mice in parentheses. WT, wild type; PLM-KO, phospholemman knockout; LV, left ventricular; LVIDD, LV internal dimension at end diastole; LVIDS, LV internal dimension at end systole; ANT, anterior wall thickness; PWT, posterior wall thickness. LV mass is given by the formula: LV mass = 1.04[(ANT + LVIDD + PWT)3 − (LVIDD)3]. Maximal +dP/dt and maximal −dP/dt are peak hemodynamic responses after 25-ng isoproterenol infusion.

*

P < 0.003, PLM-KO vs. WT.