Rj. Pearson et al., DOPAMINERGIC RECEPTOR-MEDIATED EFFECTS IN THE MESENTERIC VASCULATURE AND RENAL VASCULATURE OF THE CHRONICALLY INSTRUMENTED NEWBORN PIGLET, Critical care medicine, 24(10), 1996, pp. 1706-1712
Objective: To determine the effects of stimulation of vascular dopamin
ergic receptor subtype 1 (dopamine-1) receptors in the renal and mesen
teric vascular beds of a neonatal model. Design: Prospective, unblinde
d, dose response evaluation in an awake animal. Setting: University re
search laboratory. Subjects: Thirty newborn piglets, obtained and inst
rumented at 1 to 3 days of age and studied 48 hrs later. Interventions
: Animals were chronically instrumented with transit time ultrasound f
low probes around the left renal and superior mesenteric arteries. The
y were then intravenously infused with either dopamine (2 to 32 mu g/k
g/min) or fenoldopam (1 to 100 mu g/kg/min), which is a selective agon
ist of the dopamine-1 receptor. Measurements and Main Results: Blood p
ressure was only significantly increased by the highest infusion rate
of dopamine (32 mu g/kg/min), from a mean of 78 mm Hg at baseline to 8
7 mm Hg. Mesenteric and renal vascular resistances were unchanged by d
opamine at any dose. Dopamine at 32 mu g/kg/min decreased renal blood
flow by 16.6 +/- 19.6 (SD) % and increased renal vascular resistance b
y 39.6 +/- 41.1% (p < .05). Mesenteric blood flow in creased by 15% at
32 mu g/kg/min (p < .05) but mesenteric vascular resistance was not a
ffected by dopamine. Fenoldopam reduced blood pressure at infusion rat
es of 5, 10, and 100 mu g/kg/min. Fenoldopam had no effect on renal va
scular resistance at any dose. Fenoldopam reduced mesenteric vascular
resistance at 5 mu g/kg/min and at all higher doses. Conclusions: Thes
e data demonstrate the absence of dopaminergic receptor-mediated vasod
ilation in the porcine neonatal renal vascular bed. In the mesenteric
artery, dopamine-1 receptor-mediated vasodilation may be obtained. Dop
amine itself, probably because of stimulation of other receptors, caus
es renal artery vasoconstriction and does not increase superior mesent
eric artery blood flow.