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. 2004 Apr 5;142(2):352–366. doi: 10.1038/sj.bjp.0705767

Table 5.

Arrhythmias elicited by PAF vehicle or by the final concentration of PAF in hearts perfused with Krebs containing elevated K+ and/or supplementation with norepinephrine (NA)

Perfusion solution modification PAF vehicle 100 nmol PAF
  VPB(%)
None 0 91*
K elevated to 8 mM 0 33
K elevated to 15 mM K 0 17
+0.1 μM NA 25 90*
K elevated to 8 mM +0.1 μM NA 17 18
K elevated to 15 mM +0.1 μM NA 75 100
  Bigeminy(%)
None 0 82*
K elevated to 8 mM 0 0
K elevated to 15 mM K 0 17
+0.1 μM NA 0 60*
K elevated to 8 mM+0.1 μM NA 0 0
K elevated to 15 mM+0.1 μM NA 58 75
  Salvo(%)
None 0 55*
K elevated to 8 mM 0 17
K elevated to 15 mM K 0 0
+0.1 μM NA 0 30
K elevated to 8 mM+0.1 μM NA 0 0
K elevated to 15 mM+0.1 μM NA 58 83
  VT(%)
None 0 45*
K elevated to 8 mM 0 0
K elevated to 15 mM K 0 0
+0.1 μM NA 0 20
K elevated to 8 mM+0.1 μM NA 0 0
K elevated to 15 mM+0.1 μM NA 45 58
  VF(%)
None 0 9
K elevated to 8 mM 0 0
K elevated to 15 mM K 0 0
+0.1 μM NA 0 0
K elevated to 8 mM+0.1 μM NA 0 0
K elevated to 15 mM+0.1 μM NA 0 0

Hearts in all groups shown were initially exposed to PAF. The data represent group incidence (%) of arrhythmias during a second exposure to PAF or PAF vehicle. The results shown refer to administration of 100 nmol PAF or identically timed bolus of PAF vehicle (data from Tables 3 and 4). The hearts were perfused with K+ and/or NA added to the perfusion solution during the second exposure to PAF (or vehicle); n=12 per group.

*

P<0.05 versus PAF vehicle.