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Consumption of a high-salt diet by ewes during pregnancy alters nephrogenesis in 5-month-old offspring

Published online by Cambridge University Press:  19 March 2012

S. H. Tay
Affiliation:
School of Animal Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia Commonwealth Scientific and Industrial Research Organisation (CSIRO) Livestock Industries, Private Bag 5, Wembley, Western Australia 6913, Australia Future Farm Industries Cooperative Research Centre, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia
D. Blache
Affiliation:
School of Animal Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia
K. Gregg
Affiliation:
Western Australian Biomedical Research Institute & Centre for Health Innovation Research Institute, School of Biomedical Sciences, Curtin University, Perth, Western Australia 6845, Australia
D. K. Revell
Affiliation:
School of Animal Biology, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia Commonwealth Scientific and Industrial Research Organisation (CSIRO) Livestock Industries, Private Bag 5, Wembley, Western Australia 6913, Australia Future Farm Industries Cooperative Research Centre, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia
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Abstract

Maternal nutrition during pregnancy can affect kidney development in the foetus, which may lead to adverse consequences in the mature kidney. It was expected that high-salt intake by pregnant ewes would lead to a reduction in foetal glomerular number but that the ovine kidney would adapt to maintain homoeostasis, in part by increasing the size of each glomerulus. Merino ewes that were fed either a control (1.5% NaCl) or high-salt (10.5% NaCl) diet during pregnancy, as well as their 5-month-old offspring, were subjected to a dietary salt challenge, and glomerular number and size and sodium excretion were measured. The high-salt offspring had 20% fewer glomeruli compared with the control offspring (P < 0.001), but they also had larger glomerular radii compared with the control offspring (P < 0.001). Consequently, the cross-sectional area of glomeruli was 18% larger in the high-salt offspring than in the control offspring (P < 0.05). There was no difference in the daily urinary sodium excretion between the two offspring groups (P > 0.05), although the high-salt offspring produced urine with a higher concentration of sodium. Our results demonstrated that maternal high-salt intake during pregnancy affected foetal nephrogenesis, altering glomerular number at birth. However, the ability to concentrate and excrete salt was not compromised, which indicates that the kidney was able to adapt to the reduction in the number of glomeruli.

Type
Physiology and functional biology of systems
Copyright
Copyright © The Animal Consortium 2012

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References

Bertram, JF, Johnson, K, Hughson, MD, Hoy, WE 2001. Renal glomerular number and size in Australian Aborigines, African Americans and white populations from the same locations: a preliminary report. Image Analysis & Stereology 20, 153156.Google Scholar
Bhasin, K, van Nas, A, Martin, LJ, Davis, RC, Devaskar, SU, Lusis, AJ 2009. Maternal low-protein diet or hypercholesterolemia reduces circulating essential amino acids and leads to intrauterine growth restriction. Diabetes 58, 559566.Google Scholar
Black, MJ, Briscoe, TA, Constantinou, M, Kett, MM, Bertram, JE 2004. Is there an association between level of adult blood pressure and nephron number or renal filtration surface area? Kidney International 65, 582588.Google Scholar
Brenner, BM, Garcia, DL, Anderson, S 1988. Glomeruli and blood pressure. Less of one, more of the other? American Journal of Hypertension 1, 335347.Google Scholar
Casson, T, Warren, BE, Schleuter, K, Parker, K 1996. On farm sheep production from saltbush pastures. Australian Journal of Agricultural Research 21, 173176.Google Scholar
Chadwick, MA, Vercoe, PE, Williams, IH, Revell, DK 2009. Dietary exposure of pregnant ewes to salt dictates how their offspring respond to salt. Physiology and Behavior 97, 437445.Google Scholar
Cullen-McEwen, L, Kett, MM, Dowling, J, Anderson, WP, Bertram, JF 2003. Nephron number, renal function, and arterial pressure in aged GDNF heterozygous mice. Hypertension 41, 335340.Google Scholar
Digby, SM, Masters, DG, Blache, D, Hynd, PI, Revell, DK 2009. Offspring born to ewes fed high salt during pregnancy have altered responses to oral salt loads. Animal 4, 8188.Google Scholar
Friberg, P, Sundelin, B, Bohman, S, Bobik, A, Nilsson, H, Wickman, A, Gustafsson, H, Petersen, J, Adams, MA 1994. Renin–angiotensin system in neonatal rats: induction of a renal abnormality in response to ACE inhibition or angiotensin II antagonism. Kidney International 45, 485492.Google Scholar
Gomez, RA, Norwood, VF 1995. Developmental consequences of the renin–angiotensin system. American Journal of Kidney Disease 26, 409431.CrossRefGoogle ScholarPubMed
Gomez, RA, Lopez, M, Fernandez, L, Chenavvsky, DR, Norwood, VF 1999. The maturing kidney: development and susceptibility. Renal Failure 21, 283291.Google Scholar
Guron, G, Friberg, P 2000. An intact renin–angiotensin system is a prerequisite for normal renal development. Journal of Hypertension 18, 123137.Google Scholar
Guron, G, Adams, MA, Sundelin, B, Friberg, P 1997. Neonatal angiotensin-converting enzyme inhibition in the rat induces persistant abnormalities in renal function and histology. Hypertension 29, 9197.Google Scholar
Hilgers, KF, Norwood, VF, Gomez, RA 1997. Angiotensin's role in renal development. Seminars in Nephrology 17, 492501.Google Scholar
Hurley, JK, Kirkpatrick, SE, Pitlick, PT, Friedman, WF, Mendoza, SA 1977. Renal responses of the fetal lamb to fetal or maternal volume expansion. Circulation Research 40, 557560.Google Scholar
Kett, MM, Bertram, JF 2004. Nephron endowment and blood pressure: what do we really know? Current Hypertension Reports 6, 133139.Google Scholar
Kiprov, DD, Colvin, RB, McCluskey, RT 1982. Focal and segmental glomerulosclerosis and proteinuria associated with renal agenesis. Laboratory Investigation 46, 275281.Google Scholar
Langenberg, C, Wan, L, Bagshaw, SM, Egi, M, May, CN, Bellomo, R 2006. Urinary biochemistry in experimental septic acute renal failure. Nephrology Dialysis Transplantation 21, 33893397.Google Scholar
Langley-Evans, SC, Welham, SJM, Jackson, AA 1999. Fetal exposure to a maternal low protein diet impairs nephrogenesis and promotes hypertension in the rat. Life Sciences 64, 965974.Google Scholar
Luyckx, VA, Brenner, BM 2005. Low birth weight, nephron number, and kidney disease. Kidney International 68, S68S77.Google Scholar
Markwick, G 2007. Primefacts 326: water requirements for sheep and cattle. New South Wales Department of Primary Industries, New South Wales, Australia.Google Scholar
Matsuoka, OT, Shibao, S, Leone, CR 2007. Blood pressure and kidney size in term newborns with intrauterine growth restriction. Sao Paulo Medical Journal 125, 8590.Google Scholar
McMillen, IC, Robinson, JS 2005. Developmental origins of the metabolic syndrome: prediction, plasticity, and programming. Physiological Reviews 85, 571633.Google Scholar
Morgan, T 2001. Interactions between sodium and angiotensin. Clinical and Experimental Pharmacology and Physiology 28, 10701073.Google Scholar
Moritz, K, Wintour, EM 1999. Functional development of the meso- and metanephros. Pediatric Nephrology 13, 171187.Google Scholar
Mulroney, SE, Woda, C, Johnson, M, Pesce, C 1999. Gender differences in renal growth and function after uninephrectomy in adult rats. Kidney International 56, 944953.CrossRefGoogle ScholarPubMed
Myers, JB, Smidt, VJ, Doig, S, Di Nicolantonio, R, Morgan, TO 1985. Blood pressure, salt taste and sodium excretion in rats exposed prenatally to high salt diet. Clinical and Experimental Pharmacology and Physiology 12, 217220.Google Scholar
Nagata, M, Scharer, K, Kriz, W 1992. Glomerular damage after uninephrectomy in young rats. I. Hypertrophy and distortion of capillary architecture. Kidney International 42, 136147.CrossRefGoogle Scholar
Norman, HC, Dynes, RA, Masters, DG 2002. Nutritive value of plants growing on saline land. In Proceedings of the 8th National Conference on Productive Use and Rehabilitation of Saline Lands, pp. 59–69. Promaco Conventions Pty Ltd, Fremantle, Australia.Google Scholar
Nyengaard, JR 1993. Number and dimensions of rat glomerular capillaries in normal development and after nephrectomy. Kidney International 43, 10491057.Google Scholar
Singh, RR, Denton, KM, Bertram, JF, Jefferies, AJ, Moritz, KM 2010. Reduced nephron endowment due to fetal uninephrectomy impairs renal sodium handling in male sheep. Clinical Science 118, 669680.Google Scholar
Wikstad, I, Celsi, G, Larsson, L, Herin, P, Aperia, A 1988. Kidney function in adults born with unilateral renal agenesis or nephrectomized in childhood. Pediatric Nephrology 2, 177182.Google Scholar
Zohdi, V, Moritz, K, Bubb, KJ, Cock, ML, Wreford, N, Harding, R, Black, MJ 2007. Nephrogenesis and the renal renin–angiotensin system in fetal sheep: effects of intrauterine growth restriction during late gestation. American Journal of Physiology – Regulatory Integrative and Comparative Physiology 293, R1267R1273.Google Scholar