Effects of subpressor doses of angiotensin II on renal hemodynamics in relation to blood pressure.

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Abstract
The renal hemodynamic response to subpressor doses of angiotensin II (AII; 0.1 and 0.5 ng/min per kg) was investigated in untreated 49-yr-old men (n = 50) representing a wide blood pressure range. Renal blood flow, renal vascular resistance (RVR), glomerular filtration rate (GFR), filtration fraction (FF), plasma renin activity (PRA), plasma AII, plasma aldosterone and the urinary excretion of Na and norepinephrine were studied. The higher the initial blood pressure the greater was the increase in RVR in response to AII infusion (P < 0.002), indicating an increased renal vascular reactivity with increase in initial blood pressure. The AII infusion gave a significant rise in RVR in both the borderline and hypertensive group, but gave no increase in RVR in the normotensive group, implying an enhanced sensitivity of the renal vasculature in the borderline and hypertensive group. The increase in RVR was greater in the hypertensive than in the borderline group, i.e., the hypertensives had a steeper dose-response curve than the borderline group, which points to the presence of structural vascular changes in the renal vessels in the hypertensives. The increase in RVR in response to AII was positively correlated to Na intake and plasma aldosterone concentration, indicating that these 2 factors might modulate the renal vascular reactivity. These factors could, however, only partly explain that RVR increased more the higher the initial blood pressure. Apparently, there is an increased reactivity of the renal vascular bed to AII in essential hypertension. The increased reactivity seems to be mediated through an increased sensitivity of the renal vasculature to AII in mild essential hypertension, and also through the presence of structural vascular changes in established hypertension. These factors may lead to a reduced excretion of Na and water and may therefore be of importance in the development and progression of essential hypertension.