Figures & data
Figure 1. Protocols for the papillary muscle experiments. BIM: bisindolylmaleimide 20 nM, BK: bradykinin 500 nM, ISO: isoproterenol 100 nM, WM: wortmannin 100 nM ↓: 3 min exposure to ISO.
![Figure 1. Protocols for the papillary muscle experiments. BIM: bisindolylmaleimide 20 nM, BK: bradykinin 500 nM, ISO: isoproterenol 100 nM, WM: wortmannin 100 nM ↓: 3 min exposure to ISO.](/cms/asset/038ef461-7ab6-4132-a169-6a9b923fbf8d/icdv_a_218635_f0001_b.gif)
Figure 2. Contractile force amplitude in response to isoproterenol in papillary muscle treated with bradykinin in combination with inhibitors to PKC or PI3-kinase. BIM: bisindolylmaleimide 20 nM, BK: bradykinin 500 nM, ISO: isoproterenol 100 nM, WM: wortmannin 100 nM: p < 0.05 compared to control.
![Figure 2. Contractile force amplitude in response to isoproterenol in papillary muscle treated with bradykinin in combination with inhibitors to PKC or PI3-kinase. BIM: bisindolylmaleimide 20 nM, BK: bradykinin 500 nM, ISO: isoproterenol 100 nM, WM: wortmannin 100 nM: p < 0.05 compared to control.](/cms/asset/47532c7c-fa94-497c-8ceb-301041d28460/icdv_a_218635_f0002_b.gif)
Table I. Contractile force amplitude. Initial values.
Figure 3. Simulated guinea pig action papillary muscle potential illustrating how APD-10, APD-50 and APD-90 were determined. Time 0 was set at maximum rate of rise of phase 0 depolarization, baseline resting membrane potential was set as the average of a 20 ms sampling sequence at 50 kHz starting at time −25 ms.
![Figure 3. Simulated guinea pig action papillary muscle potential illustrating how APD-10, APD-50 and APD-90 were determined. Time 0 was set at maximum rate of rise of phase 0 depolarization, baseline resting membrane potential was set as the average of a 20 ms sampling sequence at 50 kHz starting at time −25 ms.](/cms/asset/c5894de3-9b6c-4a39-b9ec-4360c339bd6d/icdv_a_218635_f0003_b.gif)