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Relationships between fatty acid status of sow plasma and that of umbilical cord, plasma and tissues of newborn piglets when sows were fed on diets containing tuna oil or soyabean oil in late pregnancy

Published online by Cambridge University Press:  09 March 2007

J. A. Rooke*
Affiliation:
Animal Biology Division, SAC, Craibstone Estate, Aberdeen AB21 9YA, UK
I. M. Bland
Affiliation:
Animal Biology Division, SAC, Craibstone Estate, Aberdeen AB21 9YA, UK
S. A. Edwards
Affiliation:
Animal Biology Division, SAC, Craibstone Estate, Aberdeen AB21 9YA, UK
*
*Corresponding author: Dr John Rooke, fax +44 (0)1224 711292, email j.rooke@ab.sac.ac.uk
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Abstract

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To investigate the relationships between maternal, umbilical cord and piglet fatty acid status, multiparous sows (six per diet) were fed on diets containing supplements (30 g/kg) of either soyabean oil or tuna oil for the last 21 d of pregnancy. The proportions of most fatty acids differed between diets: in particular, the tuna-oil-containing diet supplied more 22:6n-3 and less 18:2n-6 fatty acids than the soyabean-oil-containing diet. Maternal plasma fatty acid concentrations (mg/l) were greater than those in umbilical plasma and 20:4n-6 and 22:6n-3 fatty acids were present in higher proportions (g/100 g fatty acids) in umbilical than maternal plasma. Feeding tuna oil increased the proportionate amounts (g/100 g fatty acids) of total n-3 fatty acids (particularly 22:6n-3) in umbilical cord, plasma and piglet tissues compared with feeding soyabean oil: in contrast, the proportion of 20:4n-6 was decreased by feeding tuna oil. Changes in piglet fatty acid proportions as a result of oil feeding were not influenced by piglet weight. While proportions of the long-chain n-3 and n-6 polyunsaturated fatty acids in piglet liver, spleen and reproductive tract (ovaries plus uterus of the female, testes of the male) correlated well with those of umbilical plasma, those in brain and retina were poorly correlated. Therefore umbilical plasma cannot be used to predict the fatty acid status of piglet brain.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1999

References

Al, MDM, Badart-Smook, A, Van Houwelingen, AC, Hasaart, THM & Hornstra, G (1995 a) Fat intake of women during normal pregnancy: relationship with maternal and neonatal essential fatty acid status. Journal of the American College of Nutrition 15, 4955.CrossRefGoogle Scholar
Al, MDM, Hornstra, G, Vanderschouw, YT, Bulstraramakers, MTEW & Huisjes, HJ (1990) Biochemical EFA status of mothers and their neonates after normal pregnancy. Early Human Development 24, 239248.CrossRefGoogle ScholarPubMed
Al, MDM, Van Houwelingen, AC, Badart-Smook, A, Hasaart, THM, Roumen, FJ & Hornstra, G (1995 b) The essential fatty acid status of mother and child in pregnancy-induced hypertension: a prospective longitudinal study. American Journal of Obstetrics and Gynecology 172, 16051614.CrossRefGoogle ScholarPubMed
Al, MDM, Van Houwelingen, AC, Kester, ADM, Hasaart, THM, De Jong, AEP & Hornstra, G (1995 c) Maternal essential fatty acid patterns during normal pregnancy and their relationship to the neonatal essential fatty acid status. British Journal of Nutrition 74, 5568.CrossRefGoogle Scholar
Berlin, E, Bhathena, SJ, McClure, D & Peters, RC (1998) Dietary Menhaden and corn oils and the red blood cell membrane lipid composition and fluidity in hyper- and normocholesterolemic miniature swine. Journal of Nutrition 128, 14211428.CrossRefGoogle ScholarPubMed
Blok, WL, Katan, MB & Van Der Meer, JWM (1996) Modulation of inflammation and cytokine production by dietary (n-3) fatty acids. Journal of Nutrition 126, 15151533.CrossRefGoogle Scholar
Burdge, GC (1998) The role of docosahexaenoic acid in brain development and fetal alcohol syndrome. Biochemical Society Transactions 26, 246251.CrossRefGoogle ScholarPubMed
Crawford, MA, Costeloe, K, Doyle, W, Leighfield, MJ, Lennon, EA & Meadows, N (1990) Potential diagnostic value of the umbilical artery as a definition of neural fatty-acid status of the fetus during its growth — the umbilical artery as a diagnostic tool. Biochemical Society Transactions 18, 761766.CrossRefGoogle ScholarPubMed
Evans, RW & Setchell, BP (1979) Lipid changes in boar spermatozoa during epididymal maturation with some observations on the flow and composition of boar rete testis fluid. Journal of Reproduction and Fertility 57, 189196.CrossRefGoogle ScholarPubMed
Fritsche, KL, Alexander, DW, Cassity, NA & Huang, S-C (1993) Maternally-supplied fish oil alters piglet immune cell fatty acid profile and eicosanoid production. Lipids 28, 677682.CrossRefGoogle ScholarPubMed
Innis, SM (1992) Plasma and red blood cell fatty acid values as indexes of essential fatty acids in the developing organs of infants fed with milk or formulas. Journal of Pediatrics 120, S78S86.CrossRefGoogle ScholarPubMed
Johnson, LA, Pursel, VG & Gerrits, RJ (1972) Total phospholipid and phospholipid fatty acids of ejaculated and epididymal semen and seminal vesicle fluids of boars. Journal of Animal Science 35, 398403.CrossRefGoogle ScholarPubMed
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 Publications.Google Scholar
Neuringer, M, Connor, WE, Lin, DS, Barstad, L & Luck, S (1986) Biochemical and functional effects of prenatal and postnatal ?-3 fatty acid deficiency on retina and brain in rhesus monkeys. Proceedings of the National Academy of Sciences USA 83, 40214025.CrossRefGoogle ScholarPubMed
Otto, SJ, Van Houwelingen, AC, Antal, M, Godfrey, K, Lopez-Jaramillo, P & Hornstra, G (1997) Maternal and neonatal essential fatty acid status in phospholipids: an international comparative study. European Journal of Clinical Nutrition 51, 232242.CrossRefGoogle ScholarPubMed
Passingham, RE (1985) Rates of brain development in mammals including man. Brain, Behaviour and Evolution 26, 167175.CrossRefGoogle ScholarPubMed
Paulenz, H, Taugbøl, O, Hofmo, PO & Saarem, K (1995) A preliminary study on the effect of dietary supplementation with cod liver oil on the polyunsaturated fatty acid composition of boar semen. Veterinary Research Communications 19, 273284.CrossRefGoogle Scholar
Reddy, S, Sanders, TAB & Obeid, O (1994) The influence of maternal vegetarian diet on essential fatty acid status of the newborn. European Journal of Clinical Nutrition 48, 358368.Google ScholarPubMed
Rioux, FM, Innis, SM, Dyer, R & MacKinnon, M (1997) Diet-induced changes in liver and bile but not brain fatty acids can be predicted from differences in plasma phospholipid fatty acids in formula- and milk-fed piglets. Journal of Nutrition 127, 370377.Google Scholar
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
Uauy, R, Birch, E, Birch, D & Peirano, P (1992) Visual and brain function measurements in studies of n-3 fatty acids requirements. Journal of Pediatrics 120, S168S180.CrossRefGoogle Scholar
Van Houwelingen, AC, Sorensen, JD, Hornstra, G, Simonis, MMG, Boris, J, Olsen, SF & Secher, NJ (1995) Essential fatty acid status in neonates after fish-oil supplementation during late pregnancy. British Journal of Nutrition 74, 723731.CrossRefGoogle ScholarPubMed
Wainwright, PE (1992) Do essential fatty acids play a role in brain and behavioral development?. Neuroscience and Biobehavioral Reviews 16, 193205.CrossRefGoogle ScholarPubMed