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. 2019 Nov 25;20(23):5927. doi: 10.3390/ijms20235927

Table 1.

Duration of severe ventricular arrhythmias during reperfusion.

Experimental Groups Ventricular Tachycardia Ventricular Fibrillation
Control 45.0 (10–142) 476.0 (198–555)
IPoC 17.0 (3–146) 5.0 (0–115) **
CPT 11.0 (0–41) 459.0 (228–555)
IPoC + CPT 68.0 (28–235) 250.5 (121–291)
DMSO 45.0 (24–123) 529.0 (205–582)
IPoCd 27.5 (3–146) 10.5 (0–141) **
SCH 50.5 (33–110) 398.5 (124–460)
IPoC + SCH 64.0 (25–128) 282.0 (112–505)
MRS 35.0 (8–99) 520.0 (233–563)
IPoC + MRS 82.5 (20–186) 263.0 (0–415)
CHE 41.0 (20–51) 467.5 (295–545)
IPoC + CHE 71.5 (38–133) 360.0 (224–460)
GLI 401.0 (260–542) ** 61.5 (18–75) *
IPoC + GLI 33.5 (12–63) 66.0 (12–90) *
ADOi10 141.0 (60–242) 91.5 (30–135) *
ADOi100 120.5 (22–195) 66.5 (0–106) *
GIPoC 39.5 (18–87) 48.0 (0–78) **

Values are expressed in seconds and correspond to median (interquartile range). Cyclopentyl theophylline (CPT), adenosine A1 receptor antagonist; dimethyl sulfoxide (DMSO), vehicle of the drugs; vehicle perfusion during IPoC procedure (IPoCd); SCH 58261(SCH), adenosine A2A receptor antagonist; MRS-1523 (MRS), adenosine A3 receptor antagonist; chelerythrine (CHE), non-selective PKC inhibitor; glibenclamide (GLI), non-selective KATP channels inhibitor; adenosine intermittent (ADOi) during reperfusion; intermittent global myocardial ischemia as postconditioning stimuli (GIPoC). * p < 0.05 and ** p < 0.01 vs. control by Kruskal-Wallis.