Why the study?
Does pretreatment with beta-blockers, calcium channel blockers, or alpha-blockers prevent acute myocardial morphological changes during brain death in a rat model?
Does pretreatment with beta-blockers, calcium channel blockers, or alpha-blockers prevent acute myocardial morphological changes during brain death in a rat model?
Pretreatment with beta-blockers prevents immediate and severe myocardial damage and interstitial edema associated with the autonomic storm of brain death in a rat model.
Beta-blockers prevented brain death-induced myocardial changes in rats; hypothesis-generating for donor management and requires clinical validation.
Our objective was to evaluate immediate acute changes in myocardial function during the autonomic storm of brain death (BD). Wistar rats were divided into four groups (n = 8/group): controls without any treatment, β-blocker (Esmolol®, 10 mg/kg), calcium channel blocker (Diltiazem®, 10 mg/kg), or alpha-blocker (Prazosin®, 0.3 mg/kg). Treatments were administered intravenously 5 min before BD induction. Echocardiography (ATL-5000, 8 MHz) was performed to measure left ventricular (LV) dimensions and fractional shortening at baseline, during BD induction and 5 min and 15 min after BD. In controls, BD was immediately associated with an increase in wall thickness and a decrease in LV cavity dimension. This myocardial wall hypertrophy was completely prevented by β-blockers, but not with calcium- and alpha-blockers. Extensive myocardial interstitial edema was found in all groups, except in the β-blocker group. Myocardial wall hypertrophy was also prevented during a longer follow-up of 180 min after BD in β-blocker group as opposed to controls. In conclusion, BD is associated with an immediate and severe myocardial damage related to an important interstitial edema which is prevented by β-blockers.
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Ferrera et al. (2010) studied this question.
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