CHANGES IN THE MATERNAL AND FETAL RENIN-ANGIOTENSIN SYSTEMS IN RESPONSE TO ANGIOTENSIN-II TYPE-1 RECEPTOR BLOCKADE AND ANGIOTENSIN-CONVERTING ENZYME-INHIBITION IN PREGNANT SHEEP DURING LATE-GESTATION

The effects of maternal administration of either an angiotensin II typ e 1 (AT(1)) receptor antagonist (GR138950) or an angiotensin-convertin g enzyme (ACE) inhibitor (captopril) on the renin-angiotensin system ( RAS) were investigated in chronically catheterized ewes and their fetu ses during late gestation. From 127 +/- 1 days of gestation until part urition at 145 +/- 2 days, each awe received daily I.V. injections of GR138950 (3 mg kg(-1), n = 10 animals) Jr captopril 13 mg kg-l, n = 6) or an equivalent volume of vehicle solution (0.9% NaCl, n = 10). On t he first day of treatment, plasma renin concentrations in the pregnant ewe increased within 2 h of administration of either GR138950 (median change followed by lower and upper quartiles (25%, 75%): +38.3 ng ml( -1) h(-1) (15.6, 80.7); P < 0.05) or captopril (+22.1 ng ml(-1) h(-1) (19.2, 28.8); P < 0.05). Maternal plasma concentrations of angiotensin II (AII) also increased by 871 pg ml(-1) (555, 1340; P < 0.05) in the GR138950-treated ewes. In the fetuses of both groups of drug-treated animals, an increase in plasma renin concentration was observed within 2 h of maternal treatment with either GR138950 (+11.6 ng ml(-1) h(-1) (1.2, 18.6); P < 0.05) or captopril (+59.3 ng ml(-1) h(-1) (41.7, 74. 6); P < 0.05). These short-term changes in circulating renin and AII c oncentrations observed in the pregnant ewe were sustained after 1 week of GR138950 administration. In addition, I week of GR133950 treatment decreased plasma angiotensinogen (Ao) concentrations in both the ewe (-0.36 mu g ml(-1) (-0.58, -0.16); P < 0.05) and the fetus (-0.43 mu g ml(-1) (-0.59, -0.09); P < 0.05). A long-term reduction in maternal p lasma AII, and an increase in fetal plasma renin concentration, were a ssociated with 1 week of captopril administration. Neither drug had an y consistent effect on plasma ACTH or cortisol concentrations in the p regnant ewe or fetus. These findings show that, during ovine pregnancy , antagonism of maternal AIT activity, either by blockade of the AT(1) receptor or by inhibition of AII synthesis, induces changes in the ci rculating components of the RAS in the mother and fetus. In both the p regnant ewe and fetus, the RAS is shown to be activated by suppression of AII activity.