Table 2.
Epi 1 APD90
(ms) |
Epi 2 API) 90
(ms) |
Endo APD90
(ms) |
EDR (ms) |
TDR (ms) |
Phase 2 reentry |
Polymorphic VT |
|
---|---|---|---|---|---|---|---|
Control | 174.7 ± 3.6 | 173.9 ± 3.3 | 184.7 ± 3.1 | 4.8 ± 1.4 | 7.3 ± 1.1 | 0/7 | 0/7 |
NS5806
5 μM |
179.2 ± 1.9 | 180.6 ± 3.4 | 183.1 ± 3.5 | 5.3 ± 0.4 | 8.7 ± 2.0 | 1/7 | 1/7 |
+Verapamil
2 μM |
201.1 ± 8.4* | 112.8 ± 13.5† | 179.7 ± 4.9 | 84.9 ± 14.4† | 66.9±11.8† | 7/7 | 7/7 |
+Milrinone
2.5 μM |
187.8 ± 3.5 | 186.5 ± 4.8‡ | 193.0 ± 4.0 | 6.5 ± 1.7§ | 7.5 ±1.3§ | 1/7 | 0/7 |
Wash out
Milrinone |
219.2 ± 8.5† | 145.1 ± 7.6* | 189.2 ± 6.9 | 74.2 ± 13.3† | 46.7 ± 9.5† | 7/7 | 6/7 |
| |||||||
| |||||||
Epi 1 APD90
(ms) |
Epi 2 APD90
(ms) |
Endo APD90
(ms) |
EDR (ms) |
TDR (ms) |
Phase 2 reentry |
Polymorphic VT |
|
| |||||||
Control | 174.7 ± 2.0 | 170.5 ± 3.1 | 184.8 ± 3.7 | 9.1 ± 2.3 | 11.0 ± 2.3 | 0/6 | 0/6 |
NS5806
5 μM |
177.3 ± 3.6 | 174.1 ± 5.9 | 187.1 ± 2.4 | 9.9 ± 3.0 | 12.1 ± 2.7 | 0/6 | 0/6 |
+Verapamil
2 μM |
206.7 ± 9.4* | 145.8 ± 9.2* | 183.3 ± 7.3 | 62.5 ± 3.1† | 43.3 ± 5.7† | 6/6 | 4/6 |
+Cilostazol
5 μM |
186.0 ± 5.3 | 191.9 ± 5.3*,‡ | 183.8 ± 6.4 | 5.6 ± 2.3§ | 12.9 ± 4.1‡ | 0/6 | 0/6 |
+Cilostazol
10 μM |
185.9 ± 5.3 | 185.1 ± 5.1‡ | 183.9 ± 6.4 | 4.8 ± 1.6§ | 7.8 ± 2.1§ | 0/6 | 0/6 |
Wash out
Cilostazol |
210.2 ± 11.2* | 135.8 ± 6.4† | 188.3 ± 9.9 | 67.8 ± 15.1† | 55.5 ± 11.2† | 6/6 | 4/6 |
APD90: action potential durations at 90% of repolarization; TDR: transmural dispersion of repolarization; EDR: epicardial dispersion of repolarization. APD90, EDR and TDR are measured in case of single stimulated beat with loss of the AP dome at EPI 2 site but not EPI 1. Results are mean ± S.E.M.
p < 0.05 and
p < 0.01 vs. control.
p < 0.05 and
p < 0.01 vs. NS5806+verapamil combination (Brugada-model). n=7 for milrinone, n=6for cilostazol. Basic cycle length=1000 ms.