Key points are not available for this paper at this time.
The effect of val-äangiotensin-II-amide on tubular sodium and water reabsorption in the rat kidney was studied by micropuncture techniques. An angiotensin infusion of 0.2–0.5 µg/min/kg caused a significant increase ( + 16 mEq/l) in the sodium concentration of tubular fluid collected from the distal tubule, as compared to collections made from the same site of the tubule during saline infusion alone. TF/P-inulin ratio remained unchanged. Glomerular filtration rate, sodium and water excretion were unaltered. During an angiotensin infusion of 1.0-1.5 µg/min/kg a similar elevation of the distal tubular sodium concentration was observed, but TF/P-inulin ratio decreased significantly. Urinary water and sodium excretion increased. An elevation of the intratubular concentration of angiotensin to 2.5 µg/ml had no effect upon tubular reabsorptive capacity, as measured by the ‘split oil-droplet method’ in the proximal or in the distal tubule. Direct application of angiotensin from the capillary side of the tubule by peritubular perfusion did not alter ‘reabsorptive half-time’ in the proximal tubule, but caused a significant prolongation of ‘reabsorptive half-time’ in the distal tubule from 35.6–67.7 sec. These results demonstrate that angiotensin, offered from the capillary side of the tubule, directly inhibits sodium reabsorption in the distal tubule.
Lowitz et al. (Wed,) studied this question.