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Am J Physiol Regul Integr Comp Physiol 293: R1267-R1273, 2007. First published June 20, 2007; doi:10.1152/ajpregu.00119.2007
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DEVELOPMENTAL PHYSIOLOGY AND PREGNANCY

Nephrogenesis and the renal renin-angiotensin system in fetal sheep: effects of intrauterine growth restriction during late gestation

Vladislava Zohdi,1 Karen M. Moritz,1 Kristen J. Bubb,2 Megan L. Cock,2 Nigel Wreford,1 Richard Harding,1 and M. Jane Black1

Departments of 1Anatomy and Cell Biology and 2Physiology, Monash University, Clayton, Victoria, Australia

Submitted 15 February 2007 ; accepted in final form 12 June 2007

Previous studies have shown that intrauterine growth restriction (IUGR) can impair nephrogenesis, but uncertainties remain about the importance of the gestational timing of the insult and the effects on the renal renin-angiotensin system (RAS). We therefore hypothesized that induction of IUGR during late gestation alters the RAS, and this is associated with a decrease in nephron endowment. Our aims were to determine the effects of IUGR induced during the later stages of nephrogenesis on 1) nephron number; 2) mRNA expression of angiotensin AT1 and AT2 receptors, angiotensinogen, and renin genes in the kidney; and 3) the size of maculae densae. IUGR was induced in fetal sheep (n = 7) by umbilical-placental embolization from 110 to 130 days of the ~147-day gestation; saline-infused fetuses served as controls (n = 7). Samples of cortex from the left kidney were frozen, and the right kidney was perfusion fixed. Total kidney volume, nephron number, renal corpuscle volume, total maculae densae volume, and the volume of macula densa per glomerulus were stereologically estimated. mRNA expression of AT1 and AT2 receptors, angiotensinogen, and renin in the renal cortex was determined. In IUGR fetuses at 130 days, body and kidney weights were significantly reduced and nephron number was reduced by 24%. There was no difference in renin, angiotensinogen, or AT1 and AT2 receptor mRNA expression levels in the IUGR kidneys compared with controls. We conclude that fetal growth restriction late in nephrogenesis can lead to a marked reduction in nephron endowment but does not affect renal corpuscle or macula densa size, or renal RAS gene expression.

kidney; nephron endowment; macula densa; stereology



Address for reprint requests and other correspondence: V. Zohdi, Dept. of Anatomy & Cell Biology, 13C, Monash Univ., Victoria 3800, Australia (e-mail: Vladislava.Zohdi{at}med.monash.edu.au)




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