Why the study?
Do angiotensin type 2 receptors modulate the haemodynamic effects of angiotensin type 1 receptors in conscious newborn lambs?
Do angiotensin type 2 receptors modulate the haemodynamic effects of angiotensin type 1 receptors in conscious newborn lambs?
In newborn lambs, AT2Rs do not counterbalance the pressor and renal vasoconstrictor effects of AT1R activation, suggesting AT1Rs predominate in mediating the haemodynamic effects of angiotensin II during this period.
AT2R inhibition adds no hemodynamic effect beyond AT1R blockade in newborn lambs; leaves open receptor balance in human neonates.
INTRODUCTION AND HYPOTHESIS: It was hypothesized that in the immediate newborn period, when the renin-angiotensin system (RAS) is activated, angiotensin type 2 receptors (AT2Rs) buffer the haemodynamic effects of angiotensin type 1 receptors (AT1Rs), as occurs in adult animals when the RAS is activated. MATERIALS AND METHODS: Arterial (systolic, diastolic, and mean) pressures (SAP, DAP, MAP), mean venous pressures (MVP) and renal blood flows (RBF) were measured in conscious, chronically instrumented lambs aged ~1 (8±2 days, N=8) and 6 weeks (41±4 days, N=11). In each animal, measurements were made before and after administration of the selective AT1R antagonist ZD 7155 (experiment one) and the selective AT2R antagonist PD123319 (experiment two) as well as both antagonists, ZD 7155 and PD 123319 (experiment three). RESULTS: Haemodynamic responses to combined inhibition of both AT1Rs and AT2Rs were similar to inhibition of AT1Rs alone: there was a significant decrease in SAP, DAP, and MAP and a significant increase in RBF within minutes of concomitant administration of ZD 7155 and PD 123319 in both age groups. These responses were similar to responses to ZD 7155 alone, whereas PD 123319 alone did not alter any of the measured variables. CONCLUSIONS: AT2Rs do not counterbalance the pressor and renal vasoconstrictor effects elicited by activation of AT1Rs in the immediate newborn period. During this time, AT1Rs appear to predominate in eliciting the haemodynamic effects of angiotensin II (ANG II), whereas the role of the upregulated AT2Rs remains elusive.
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Vinturache et al. (2014) studied this question.
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