Why the study?
Does bevantolol affect cardiac performance and prevent ventricular fibrillation in anesthetized open-chest pigs?
Does bevantolol affect cardiac performance and prevent ventricular fibrillation in anesthetized open-chest pigs?
Bevantolol demonstrates negative chronotropic and inotropic effects while preventing early-phase ventricular fibrillation following coronary occlusion in a porcine model.
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Bevantolol may suppress early VF post-occlusion in pigs despite reducing cardiac output; leaves open any human antiarrhythmic role.
The cardioselective beta‐adrenoceptor antagonist bevantolol (1‐[(3,4‐dimethoxyphenethyl)amino]‐3‐(m‐tolyloxy)‐2‐propanol monohydrochloride) was studied for its effects on cardiac performance and on coronary artery occlusion‐induced ventricular fibrillation in anesthetized open‐chest pigs. In doses of 0.5‐‐3.0 mg·kg −1 the drug caused dose‐dependent decreases in cardiac output (10‐‐35%) that were primarily due to a negative chronotropic action, as heart rate decreased considerably more (10‐‐25%) than stroke volume (0‐‐15%). The decrease in stroke volume appeared to be due to a decrease in maxLVdP/dt (up to 40%) and a mild vasoconstriction (≥20%) of the systemic arterial vascular bed. Myocardial blood flow (25‐‐45%) and O 2 extraction both decreased, but cerebral blood flow was well preserved. Decreases in perfusion of some organs (kidneys, liver, and stomach) were similar to those in cardiac output, but that of the small intestine was not significantly affected. After ligation of the left anterior descending coronary artery at its midpoint, bevantolol prevented ventricular fibrillation during the earliest phase of ectopic activity, but was ineffective during the second phase of the early arrhythmias.
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Hartog et al. (1986) studied this question.
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