Pediatr. Res. 15: 1248Res. 15: -1255 one can speculate that a decrease in glomerular vascular resistcatheterized fetal lambs between 106 and 140 days of gestation ance is a major determinant in the postnatal increase in glomerular (term, 145 days) and in six newborn lambs between 3 and 19 days perfusion rate and GFR. of age. The present study demonstrates for the first time in lambs that the nephrogenic zone disappears around 130 days of gestation and that the total glomerular counts per kidney in fetuses over Previous studies (5,13,14,16) have demonstrated that the 130 days (4682% + 41173 glomeruli per kidney) is not significantly cortical blood flow is distributed preferentially to the juxtameduldifferent than in newborn lambs (433704 + 21553). Glomerular lary area of the cortex during early postnatal life, and with density, determined in four cortical zones (zone I being the out-maturation, the development of cortical flow follows a centrifugal ermost portion of the cortex) did not show any significant changes pattern. Spitzer and Brandis (26) also demonstrated that the during fetal life; however, significant decreases in glomerular maturation of glomerular filtration rate (GFR) closely follows the density were observed in each cortical zone after birth. The relative developmental pattern of cortical blood flow, M~~~ recently, distribution of glomeruli during fetal life decreased in the outer ~~~~i~ and ~~~i~ (31, studying factors modulating the changes in portion (zones I and 11) and increased in the inner Portion (zones GFR during maturation, have suggested that glomerular perfusion 111 and IV) of the cortex as fetuses matured and approached term. rate (GPR) is an important determinant of the increase in GFR After birth, this difference became even more prominent; the outer during postnatal life, cortical fraction (zone I) decreased from 49.6 + 2.9% in fetuses of studies from our laboratory have demonstrated that during less than 120 days 37-8 * (P < Oeo5) in lambs, fetal life G F R increases at the same rate as the fetal body weight whereas the fraction found in zone 111 increased from 14.9 + 1.3% and kidney weight (18, 21). ~h~~~ observations are contrary to to 20.8 + 0.7% ( P < 0.05). Small but significant increases in what occurs after birth, where the increase in G F R is disproporglomerular filtration rate (GFR) ( P < 0.01) and total renal blood tionately higher than the concomitant rise in body weight and flow (P < 0.05) were observed during fetal life: GFR and total kidney weight (1 1, 20). Factors responsible for the difference in renal blood flow increased, respectively, from 1.84 2 0.11 and 37 the developmental patterns of fetal and newborn G F R have not f 2 ml/min in fetuses
The renal and adrenal responses to a continuous infusion of the angiotensin-converting enzyme (ACE) inhibitor captopril were studied in 27 chronically catheterized sheep fetuses (less than 120 days gestation, n = 15, and greater than 130 days gestation, n = 12; term being 145 days) and in 12 newborn lambs between 8 and 21 days of age. Total renal blood flow did not change during ACE inhibition. However, the renal vascular resistance decreased significantly in newborn lambs (-21.8 +/- 5.7%) and in fetuses greater than 130 days (-21.7 +/- 4.7%) but not in fetuses less than 120 days. A significant decrease in filtration fraction (-19.2 +/- 6.5%) was observed in newborn lambs. No changes in urinary kallikrein and prostaglandin excretion rate were observed during ACE inhibition in any group of animals. ACE inhibition produced similar declines in blood pressure in both groups of fetuses (-10.2 +/- 3% in fetuses less than 120 days and -9.5 +/- 4.6% in fetuses greater than 130 days) and in newborn lambs (-13.4 +/- 2.1%). The percent changes in plasma renin activity were similar in all groups of animals. However, a significant decline in plasma aldosterone concentration was observed only in newborn lambs (from 130 +/- 31 to 64 +/- 9 pg/ml). These results suggest that the renin-angiotensin system might have physiological significance during maturation, but that this role seems to be more important in near-term fetuses (greater than 130 days) and postnatally than early in gestation.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.