Table 1.
Parameter | WT Ctrl | WT LPS | IL-37tg Ctrl | IL-37tg LPS | WT LPS + rIL-37 |
---|---|---|---|---|---|
Heart rate (bpm) | 430 ± 36 | 528 ± 56* | 437 ± 29 | 520 ± 73# | 510 ± 61* |
Developed pressure (mmHg) | 78.7 ± 7.8 | 47.0 ± 3.6* | 80.0 ± 11 | 67.2 ± 7.4#† | 65.3 ± 9.8† |
End-systolic volume (μl) | 8.0 ± 5.5 | 24.5 ± 2.9* | 9.1 ± 2.2 | 14.9 ± 2.4#† | 16.5 ± 2.8*† |
End-diastolic volume (μl) | 20.2 ± 3.9 | 31.1 ± 6.1* | 20.6 ± 3.1 | 24.2 ± 2.9 | 25.1 ± 4.4 |
Ejection Fraction (%) | 60.4 ± 9.0 | 21.2 ± 4.6* | 55.8 ± 12 | 38.4 ± 5.3#† | 34.3 ± 6.1*† |
Cardiac output (ml/min) | 5.3 ± 0.9 | 3.2 ± 0.3* | 5.1 ± 1.2 | 4.7 ± 0.4† | 4.4 ± 0.8† |
WT and IL-37tg old mice were treated with lipopolysaccharide (LPS, 0.5 mg/kg, iv) or normal saline. In a separate group of WT old mice, recombinant IL-37 (rIL-37, 0.05 mg/kg, iv) was administered 30 minutes after injection of LPS. WT old mice had reduced left ventricle (LV) function, including the developed pressure, ejection fraction and cardiac output, at 6 hours after treatment with LPS. IL-37tg old mice displayed better LV function after treatment with LPS in comparison to WT old mice. Treatment with recombinant IL-37 also improved LV function in WT old mice exposed to LPS. Data are expressed as mean ± SD. n=6 mice in each group; one-tailed ANOVA;
P<0.05 vs. WT old control (Ctrl);
P<0.05 vs. IL-37tg old control;
P<0.05 vs. WT old mice treated with LPS alone.