Key result
In open-chest pigs with acute myocardial ischaemia, prenalterol improved aortic flow and LV dp/dt, an effect primarily driven by a significant increase in heart rate.
Why the study?
Does prenalterol improve haemodynamics in a pig model of acute myocardial ischaemia?
Does prenalterol improve haemodynamics in a pig model of acute myocardial ischaemia?
In a pig model of acute myocardial ischemia, prenalterol improved hemodynamics primarily by increasing heart rate rather than stroke volume.
Answers are grounded in this paper and cite their sources.
Prenalterol may stabilize hemodynamics in acute ischemia; extends RCT data on sympathomimetics to porcine MI models.
The haemodynamic effects of prenalterol, a new sympathomimetic agent, have been studied in anaesthetized open-chest pigs with acute myocardial ischaemia provoked by left anterior descending coronary artery ligation. A group of eight animals was infused with saline and served as control (C). In both groups the ligation of the left anterior descending coronary artery determined a significant (P less than 0.05) reduction of aortic flow, maximum left ventricular (LV) dp/dt with no changes in heart rate. The infusion of a first dose of 30 micrograms/kg of prenalterol restored the depressed haemodynamics but increased significantly the heart rate in the prenalterol group while the saline infused group did not show any significant changes. The haemodynamic effects of prenalterol were still evident 25 min after the infusion. The subsequent administration of a second dose of 60 micrograms/kg of prenalterol resulted in a further improvement of the aortic flow, LV dp/dt and heart rate which reached values higher than in the basal condition. The positive inotropic effect was not associated with changes in stroke volume, therefore the increase in aortic flow was essentially due to an increase of the heart rate. It is concluded that prenalterol is a powerful inotropic agent in acutely infarcted animals. Its action on aortic flow appears to be related to an increase in heart rate in contrast to some previous observations.
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Branzi et al. (1983) studied Acute myocardial ischaemia. Prenalterol vs. Saline was evaluated on Haemodynamic effects (aortic flow, maximum LV dp/dt, heart rate). In open-chest pigs with acute myocardial ischaemia, prenalterol improved aortic flow and LV dp/dt, an effect primarily driven by a significant increase in heart rate.
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