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Feeding pregnant ewes a high-salt diet or saltbush suppresses their offspring’s postnatal renin activity

Published online by Cambridge University Press:  01 July 2009

M. A. Chadwick*
Affiliation:
School of Animal Biology, University of Western Australia, Nedlands, Western Australia 6009, Australia Commonwealth Scientific and Industrial Research Organisation (CSIRO) Livestock Industries, PMB 5 Wembley, Western Australia 6913, Australia Future Farm Industries Co-operative Research Centre, Australia
I. H. Williams
Affiliation:
School of Animal Biology, University of Western Australia, Nedlands, Western Australia 6009, Australia
P. E. Vercoe
Affiliation:
School of Animal Biology, University of Western Australia, Nedlands, Western Australia 6009, Australia Future Farm Industries Co-operative Research Centre, Australia
D. K. Revell
Affiliation:
School of Animal Biology, University of Western Australia, Nedlands, Western Australia 6009, Australia Commonwealth Scientific and Industrial Research Organisation (CSIRO) Livestock Industries, PMB 5 Wembley, Western Australia 6913, Australia Future Farm Industries Co-operative Research Centre, Australia
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Abstract

If ewes consumed a high-salt diet or saltbush during the last 3 months of pregnancy and for 3 weeks after birth, we expected the renin activity of their lamb to be suppressed at birth and at 3 weeks of age. We also expected an increase in the concentration of cations other than sodium in the ewe’s milk and an increase in the plasma Na concentration of the lamb at birth. To test these hypotheses, Merino ewes were fed a high-salt diet (14% NaCl) in an animal house and compared to control ewes eating a control diet (2% NaCl). In addition, we compared ewes grazing saltbush (about 13% salt in diet) to ewes grazing pasture from day 60 of pregnancy to 3 weeks after birth. Lambs born to ewes consuming saltbush had 85% lower (P < 0.001) renin activity than offspring from ewes consuming pasture at 3 weeks of age. Similarly, lambs born to ewes consuming a high-salt diet had 20% lower renin activity at birth and 3 weeks (P = 0.07). Feeding ewes a high-salt diet or saltbush altered the mineral composition of the milk; the largest change was a 10% increase in K levels (P ⩽ 0.05). Consuming a high-salt diet or saltbush lowered the plasma Na of ewes at 130 days of gestation (by 3–5 mmol/l; P < 0.001), but only lambs from ewes fed the high-salt diet had a lower plasma Na at birth (P < 0.05). Suppression of the renin activity of lambs could lead to permanent physiological changes in salt balance in later life.

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Full Paper
Copyright
Copyright © The Animal Consortium 2009

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References

Abu-Zanat, MMW, Tabbaa, MJ 2006. Effect of feeding Atriplex browse to lactating ewes on milk yield and growth rate of their lambs. Small Ruminant Research 64, 152161.CrossRefGoogle Scholar
Alves da Silva, AA, de Noronha, IL, de Oliveira, IB, Malheiros, DMC, Heimann, JC 2003. Renin–angiotensin system function and blood pressure in adult rats after perinatal salt overload. Nutrition, Metabolism and Cardiovascular Diseases 13, 133139.CrossRefGoogle Scholar
Baharin, K, Beilharz, RG 1977. A comparison of the performance of single and twin born Corriedale ewes and lambs. Australian Journal of Experimental Agriculture and Animal Husbandry 17, 242246.CrossRefGoogle Scholar
Balbi, AP, Costa, RS, Coimbra, TM 2004. Postnatal renal development of rats from mothers that received increased sodium intake. Pediatric Nephrology 19, 12121218.CrossRefGoogle ScholarPubMed
Broughton Pipkin, F, Lumbers, ER, Mott, JC 1974. Factors influencing plasma renin and angiotensin II in the conscious pregnant ewe and its fetus. Journal of Physiology 243, 619636.CrossRefGoogle Scholar
Contreras, RJ 1993. High NaCl intake of rat dams alters maternal behavior and elevates blood pressure of adult offspring. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 264, R296R304.CrossRefGoogle ScholarPubMed
Curtis, KS, Krause, EG, Wong, DL, Contreras, RJ 2004. Gestational and early postnatal dietary NaCl levels affect NaCl intake, but not stimulated water intake, by adult rats. American Journal of Physiology-Regulatory Integrative and Comparative Physiology 286, R1043R1050.CrossRefGoogle Scholar
Dancis, J, Springer, D 1970. Fetal homeostasis in maternal malnutrition: potassium and sodium deficiency in rats. Pediatric Research 4, 345351.CrossRefGoogle ScholarPubMed
Deloof, S, De Seze, C, Montel, V, Chatelain, A 2000. Atrial natriuretic peptide and aldosterone secretions and atrial natriuretic peptide-binding sites in kidneys and adrenal glands of pregnant and fetal rats in late gestation in response to a high salt diet. European Journal of Endocrinology 142, 524532.CrossRefGoogle ScholarPubMed
Desai, M, Guerra, C, Wang, S, Ross, MG 2003. Programming of hypertonicity in neonatal lambs: resetting of the threshold for vasopressin secretion. Endocrinology 144, 43324337.CrossRefGoogle ScholarPubMed
Digby, SN, Masters, DG, Blache, D, Blackberry, MA, Hynd, PI, Revell, DK 2008. Reproductive capacity of Merino ewes fed a high-salt diet. Animal 2, 13531360.CrossRefGoogle ScholarPubMed
Dlouha, H, Erdosova, R, Kraus, M, Skopkova, J 1973. The effect of sodium intake on maternal milk electrolytes and aldosterone, corticosterone and 18-hydroxydeoxy-corticosterone production in the offspring of rats. Biology of the Neonate 22, 3849.CrossRefGoogle ScholarPubMed
Fleischman, AR, Oakes, GK, Epstein, MF, Catt, KJ, Chez, RA 1975. Plasma renin activity during ovine pregnancy. American Journal of Physiology 228, 901904.CrossRefGoogle ScholarPubMed
Giebisch, G, Stanton, B 1979. Potassium transport in the nephron. Annual Review of Physiology 41, 241256.CrossRefGoogle ScholarPubMed
Gomez, RA, Norwood, VF 1995. Developmental consequences of the renin–angiotensin system. American Journal of Kidney Diseases 26, 409431.CrossRefGoogle ScholarPubMed
Gamble, JL, Putnam, MC, McKhann, CF 1929. The optimal water requirement in renal function: I. Measurements of water drinking by rats according to increments of urea and of several salts in the food. American Journal of Physiology 88, 571580.CrossRefGoogle Scholar
Hilgers, KF, Norwood, VF, Gomez, RA 1997. Angiotensin’s role in renal development. Seminars in Nephrology 17, 492501.Google ScholarPubMed
Ingelfinger, J, Haveran, L, Hsu, CL, Woods, LL 1998. Maternal low protein or high salt diet in the perinatal period suppresses newborn intrarenal renin–angiotensin system (RAS) and programs for hypertension in adult offspring. Pediatric Research 43, 309312.CrossRefGoogle Scholar
Masters, DG, Norman, HC, Dynes, RA 2001. Opportunities and limitations for animal production from saline land. Asian-Australasian Journal of Animal Sciences 14, 199211.Google Scholar
Matsusaka, T, Miyazaki, Y, Ichikawa, I 2002. The renin angiotensin system and kidney development. Annual Review of Physiology 64, 551561.CrossRefGoogle ScholarPubMed
Meyer, JH, Weir, WC 1954. The tolerance of sheep to high intakes of sodium chloride. Journal of Animal Science 13, 443449.CrossRefGoogle Scholar
Morgan, T 2001. Interactions between sodium and angiotensin. Clinical and Experimental Pharmacology and Physiology 28, 10701073.CrossRefGoogle ScholarPubMed
Nose, H, Sugimoto, E, Okuno, T, Morimoto, T 1987. Changes in blood volume and plasma sodium concentration after water intake in rats. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 253, R15R19.CrossRefGoogle ScholarPubMed
Park, YW, Juarez, M, Ramos, M, Haenlein, GFW 2007. Physio-chemical characteristics of goat and sheep milk. Small Ruminant Research 68, 88113.CrossRefGoogle Scholar
Potter, BJ, McIntosh, GH 1974. Effect of salt water ingestion on pregnancy in the ewe and on lamb survival. Australian Journal of Agricultural Research 25, 909917.CrossRefGoogle Scholar
Richardson Morton, KD, Johnson, MD, Van de Kar, LD 1995. Serotonin and stress-induced increases in renin secretion are not blocked by sympathectomy/adrenal medullectomy but are blocked by beta antagonists. Brain Research 698, 185192.CrossRefGoogle Scholar
SCARM (Standing Committee on Agricultural and Resource Management) 1990. Feeding standards for Australian livestock: ruminants. CISRO Publications, Melbourne, Australia.Google Scholar
Stricker, EM, Hoffmann, ML, Riccardi, CJ, Smith, JC 2003. Increased water intake by rats maintained on a high NaCl diet: analysis of ingestive behaviour. Physiology and Behavior 79, 621631.CrossRefGoogle Scholar
Vijande, M, Brime, JI, Lopez-Sela, P, Costales, M, Arguelles, J 1996. Increased salt preference in adult offspring raised by mother rats consuming excessive amounts of salt and water. Regulatory Peptides 66, 105108.CrossRefGoogle ScholarPubMed
Wheeler, JL, Reardon, TF, Hedges, DA, Rocks, RL 1971. The contribution of the conceptus to weight change in pregnant Merino ewes at pasture. Journal of Agricultural Science 76, 347353.CrossRefGoogle Scholar