Low-Dose Adrenaline Reduces Blood Pressure Acutely in Anesthetized Pigs Through a beta(2)-Adrenergic Pathway
Research output: Contribution to journal › Journal article › peer-review
Adrenaline (epinephrine) is one of the prime messengers of the fight-or-flight response, favoring the activation of beta-adrenergic receptors. Although general vasoconstriction to nonessential tissues is imperative, the vasodilatory effect of beta-adrenergic receptor activation contends with this. We aimed to determine the dosedependent effects of adrenaline on hemodynamics and to test whether adrenaline could lower blood pressure (BP) through a beta(2)-adrenergic pathway. Nineteen Danish landrace pigs were used to pharmacologically probe the hemodynamic effect of adrenaline. Pigs were anesthetized, intubated, and electrocardiogram, systolic BP (SBP), diastolic BP (DBP), and left ventricular pressure (LVP) were monitored continuously. First, we tested the dose-dependent effects of adrenaline (0.01-10 mu g/kg). Second, we determined the response to adrenaline (0.3 mu g/kg) after atropine, prazosin, and propranolol pretreatment. Finally, we tested the hemodynamic effect of salbutamol in a subset of pigs. All doses of adrenaline increased heart rate, while BP showed a biphasic response: At low doses, adrenaline decreased SBP from 118 +/- 3 to 106 +/- 4 mm Hg (n = 15; P < 0.05) and DBP from 86 +/- 3 to 71 +/- 3 (n = 15; P < 0.05), while at high doses, SBP and DBP increased. LVP showed a similar pattern, with a tendency of decreased pressure at low doses, and an increased pressure at high doses (P < 0.05). Pretreatment with autonomic blockers revealed that the increase in BP was due to alpha-adrenergic activity, while the decrease was due to beta-adrenergic activity. In confirmation, beta-adrenergic activation through salbutamol showed a similar decrease in SBP, DBP, and LVP. We conclude that adrenaline dose-dependently increases heart rate, while producing a biphasic response in BP with a decrease at low doses and an increase at high doses in an anesthetized, large-animal model.
|Journal||Journal of Cardiovascular Pharmacology|
|Publication status||Published - 2019|
- epinephrine, porcine, vascular compliance, adrenergic