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. Author manuscript; available in PMC: 2018 Jul 1.
Published in final edited form as: Cytokine. 2017 Feb 24;95:55–63. doi: 10.1016/j.cyto.2017.02.008

Table 1.

Left ventricle function parameters

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.