Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-23T07:25:17.472Z Has data issue: false hasContentIssue false

Feeding tuna oil to the sow at different times during pregnancy has different effects on piglet long-chain polyunsaturated fatty acid composition at birth and subsequent growth

Published online by Cambridge University Press:  09 March 2007

J. A. Rooke*
Affiliation:
Animal Biology Division, Scottish Agricultural College, Craibstone Estate, Aberdeen AB21 9YA, UK
A. G. Sinclair
Affiliation:
Animal Biology Division, Scottish Agricultural College, Craibstone Estate, Aberdeen AB21 9YA, UK
S. A. Edwards
Affiliation:
Animal Biology Division, Scottish Agricultural College, Craibstone Estate, Aberdeen AB21 9YA, UK
*
*Corresponding author: Dr J. A. Rooke, fax +44 (0) 1224 711292, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

In an attempt to prevent decreases in piglet 20 : 4n-6 status at birth while increasing 22 : 6n-3 status, multiparous sows (eight per treatment) were allocated to one of three different treatments: a basal diet fed from day 63 of pregnancy to term; basal diet supplemented with tuna oil (17·5 g/kg) from day 63 to day 91 and then basal diet alone from day 92 to term; basal diet alone from day 63 to day 91 and then basal diet supplemented with tuna oil from day 92 to term. Tuna oil supplementation increased mainly 22 : 6n-3 intake. Supplementation with tuna oil between day 92 and term increased 22 : 6n-3 to a greater extent in all piglet tissues (brain, liver, retina and the remaining carcass) at birth than supplementation with tuna oil between days 63 and 91. However, while piglet 20 : 4n-6 decreased to a greater extent in liver and carcass when diets were supplemented with tuna oil between days 92 and term than between days 63 and 91, in the brain and retina, the reverse was true; 20 : 4n-6 was decreased to a greater extent between days 63 and 91 than between 92 and term. The effect of pregnancy nutrition on the growth of piglets until 7 d postweaning (35 d of age) was assessed after removing any residual effects of pregnancy treatment by cross-fostering some piglets at birth. Piglets, the diets of whose dams had been supplemented with tuna oil during pregnancy, grew faster during the first 35 d of life than the progeny of sows fed only the basal diet. Feeding tuna oil to sows at different times during pregnancy therefore did not prevent decreases in piglet 20 : 4n-6 status at birth, but did suggest that changes in piglet brain 20 : 4n-6 status between days 63 and 91 of pregnancy were not reversible by later nutrition. Supplementing the diet of the pregnant sow with tuna oil had beneficial effects on postnatal piglet growth.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2001

References

Act of Parliment (1986) Animal (Scientific Procedures) Act 1986. London: H.M. Stationery Office.Google Scholar
Atkinson, T, Fowler, VR, Garten, GA & Lough, AK (1972) A rapid method for the accurate determination of lipid in animal tissues. Analyst 97, 562588.CrossRefGoogle ScholarPubMed
Carlson, SE, Cooke, RJ, Werkman, SH & Tolley, EA (1992) First year growth of preterm infants fed standard compared to marine oil n-3 supplemented formula. Lipids 27, 901907.CrossRefGoogle ScholarPubMed
Carlson, SE, Werkman, SH, Peeples, JM, Cooke, RJ & Tolley, EA (1993) Arachidonic acid status correlates with first year growth in preterm infants. Proceedings of the National Academy of Sciences USA 90, 10731077.CrossRefGoogle ScholarPubMed
Clandinin, MT, Chappell, JE, Leong, S, Heim, T, Swyer, PR & Chance, GW (1980) Intrauterine fatty acid accretion rates in human brain: implications for fatty acid requirements. Early Human Development 4, 121129.CrossRefGoogle ScholarPubMed
Cordoba, R, Pkiyach, S, Rooke, JA, Edwards, SA, Penny, PC & Pike, I (2000) The effect of feeding salmon oil during pregnancy on causes of piglet deaths prior to weaning. In Proceedings of the British Society of Animal Science 2000, P. 105. Edinburk, UK: British Society of Animal Science.Google Scholar
Cox, SE (1999) The fetal origins hypothesis: an overview and implications. Nutrition Abstracts and Reviews 69A, 929935.Google Scholar
Farnworth, ER & Kramer, JKG (1988) Fetal pig development in sows fed diets containing different fats. Canadian Journal of Animal Science 68, 249256.CrossRefGoogle Scholar
Grimble, RF (1998) Modification of inflammatory aspects of immune function by nutrients. Nutrition Research 7, 12971317.CrossRefGoogle Scholar
Kurlak, LO & Stephenson, TJ (1999) Plausible explanations for effects of long-chain polyunsaturated fatty acids (LCPUFA) on neonates. Archives of Diseases in Childhood 80, F148F154.CrossRefGoogle ScholarPubMed
Kushner, I & Mackiewicz, A (1993) The acute-phase response: an overview. In Biology, Biochemistry, and Clinical Applications pp. 319 [Mackiewicz, A, Kushner, I and Baumann, H, editors]. Boca Raton, FL: CRC Press.Google Scholar
McCracken, BA, Gaskins, HR, Ruwe-Kaiser, PJ, Klasing, KC & Jewell, DE (1995) Diet-dependent and diet-independent metabolic responses underlie growth stasis of pigs at weaning. Journal of Nutrition 125, 28382845.Google ScholarPubMed
McCracken, BA, Spurlock, ME, Roos, MA, Zuckermann, FA & Gaskins, HR (1999) Weaning anorexia may contribute to local inflammation in the piglet small intestine. Journal of Nutrition 129, 613619.CrossRefGoogle ScholarPubMed
Mahan, DC & Lepine, AJ (1991) Effect of pig weaning weight and associated nursery feeding programmes on subsequent performance to 105 kgs body weight. Journal of Animal Science 69, 13701378.CrossRefGoogle Scholar
Ministry of Agriculture, Fisheries and Food (1992) Analysis of Agricultural Materials, 2nd ed. London: H.M. Stationery Office.Google Scholar
Ministry of Agriculture, Fisheries and Food (1993) Prediction of the Energy Value of Compound Feedingstuffs for Farm Animals. London: MAFF PublicationsGoogle Scholar
Passingham, RE (1985) Rates of brain development in mammals including man. Brain, Behaviour and Evolution 26, 167175.CrossRefGoogle ScholarPubMed
Raclot, T & Groscolas, R (1993) Differential mobilization of white adipose tissue fatty acids according to chain length, unsaturation, and positional isomerism. Journal of Lipid Research 54, 15131526.Google Scholar
Ramsay, TG, Karousis, J, White, ME & Wolverton, CK (1991) Fatty acid metabolism by the porcine placenta. Journal of Animal Science 69, 36453654.CrossRefGoogle ScholarPubMed
Rooke, JA, Bland, IM & Edwards, SA (1998) Effect of feeding tuna oil or soyabean oil as supplements to sows in late pregnancy on piglet tissue composition and viability. British Journal of Nutrition 80, 273280.CrossRefGoogle ScholarPubMed
Rooke, JA, Bland, IM & Edwards, SA (1999) Relationships between fatty acid status of sow plasma and that of umbilical cord and plasma and tissues of new-born piglets when sows were fed diets containing tuna oil or soyabean oil in late pregnancy. British Journal of Nutrition 82, 213221.CrossRefGoogle ScholarPubMed
Rooke, JA, Shanks, M & Edwards, SA (2000) Effect of offering maize, linseed or tuna oils throughout pregnancy and lactation on sow and piglet tissue composition and piglet performance. Animal Science 71, 289299.CrossRefGoogle Scholar
Rooke, JA, Sinclair, AG, Ewen, M & Birnie, LM (2001) Responses in piglet tissue composition to increasing maternal intake of long chain n-3 polyunsaturated fatty acids. Proceedings of the Nutrition Society 60, 71A.Google Scholar
Ruwe, PJ, Wolverton, CK, White, ME & Ramsay, TG (1991) Effect of maternal fasting on fetal and placental lipid metabolism in swine. Journal of Animal Science 69, 19351944.CrossRefGoogle ScholarPubMed
Skinner, JG & Roberts, L (1994) Haptoglobin as an indicator of infection in sheep. Veterinary Record 134, 3336.CrossRefGoogle ScholarPubMed
Speake, BK, Cerolini, C, Maldjian, A & Noble, RC (1997) The preferential mobilisation of C20 and C22 polyunsaturated fatty acids from the adipose tissue of the chick embryo: potential implications regarding the provision of essential fatty acids for neural development. Biochimica et Biophysica Acta 1345, 317326.CrossRefGoogle ScholarPubMed
Spurlock, ME, Frank, GR, Willis, GM, Kuske, JL & Cornelius, SG (1997) Effect of dietary energy source and immunological challenge on growth performance and immunological variables in growing pigs. Journal of Animal Science 75, 720726.CrossRefGoogle ScholarPubMed
Sweasey, D, Patterson, DSP & Glancy, EM (1976) Biphasic myelination and the fatty acid composition of cerebrosides and cholesterol esters in the developing central nervous system of the domestic pig. Journal of Neurochemistry 27, 375380.CrossRefGoogle ScholarPubMed
Thulin, AJ, Allee, GL, Harmon, DL & Davis, DL (1989) Utero-placental transfer of octanoic, palmitic and linoleic acids during late gestation in gilts. Journal of Animal Science 67, 738745.CrossRefGoogle ScholarPubMed
Uauy, R, Mena, P & Rojas, C (2000) Essential fatty acids: structural and functional role. Proceedings of the Nutrition Society 59, 315.CrossRefGoogle ScholarPubMed
Varley, M (1995) The Neonatal Pig. Development and Survival. Wallingford, Oxon.: CAB International.Google Scholar
Whittemore, CT & Yang, H (1989) Physical and chemical composition of the body of breeding sows with differing body subcutaneous fat depth at parturition, differing nutrition during lactation and differing litter size. Animal Production 48, 203212.CrossRefGoogle Scholar
Williams, NH, Stahly, TS & Zimmerman, DR (1997) Effect of chronic immune system activation on the rate, efficiency, and composition of growth and lysine needs of pigs fed from 6 to 27 kg. Journal of Animal Science 75, 24632471.CrossRefGoogle Scholar