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Effects of dietary fat and conjugated linoleic acid on plasma metabolite concentrations and metabolic responses to homeostatic signals in pigs

Published online by Cambridge University Press:  09 March 2007

E. Ostrowska
Affiliation:
Agriculture Victoria, Victorian Institute of Animal Science, Werribee, Victoria 3030, Australia
R. F. Cross
Affiliation:
Swinburne University of Technology, Hawthorn, Victoria 3122, Australia
M. Muralitharan
Affiliation:
Deakin University, Geelong, Victoria, Australia
D. E. Bauman
Affiliation:
Cornell University, Ithaca, NY 14853, USA
F. R. Dunshea*
Affiliation:
Agriculture Victoria, Victorian Institute of Animal Science, Werribee, Victoria 3030, Australia
*
*Corresponding author: Associate Professor Frank R. Dunshea, fax +61 3 9 742 0400, email [email protected]
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Abstract

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Sixteen female cross-bred (Large White × Landrace) pigs (initial weight 65 kg) with venous catheters were randomly allocated to four treatment groups in a 2×2 factorial design. The respective factors were dietary fat (25 or 100 g/kg) and dietary conjugated linoleic acid (CLA; 0 or 10 g CLA-55/kg). Pigs were fed every 3 h (close to ad libitum digestible energy intake) for 8 d and were bled frequently. Plasma glucose and non-esterified fatty acid (NEFA) responses to insulin and adrenaline challenges were determined on day 8. Plasma concentrations of NEFA were significantly increased (10·5 and 5·4 % for low- and high-fat diets respectively, P=0·015) throughout the experiment, suggesting that there was a possible increase in fat mobilisation. The increase in lipolysis, an indicator of ß-adrenergic stimulated lipolysis, was also evident in the NEFA response to adrenaline. However, the increase in plasma triacylglycerol (11·0 and 7·1 % for low- and high-fat diets respectively, P=0·008) indicated that CLA could have reduced fat accretion via decreased adipose tissue triacylglycerol synthesis from preformed fatty acids, possibly through reduced lipoprotein lipase activity. Plasma glucose, the primary substrate for de novo lipid synthesis, and plasma insulin levels were unaffected by dietary CLA suggesting that de novo lipid synthesis was largely unaffected (P=0·24 and P=0·30 respectively). In addition, the dietary CLA had no effect upon the ability of insulin to stimulate glucose removal.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2002

References

Albright, K, Liu, KL, Storkson, JM, Hentges, E, Lofgren, P, Simeca, J, Cook, ME & Pariza, M (1996) Body composition repartitioning following the removal of dietary conjugated linoleic acid. Journal of Animal Science 74, 152.Google Scholar
Baumgard, LH, Corl, BA, Dwyer, DA & Bauman, DE (2002) Effects of conjugated linoleic acid (CLA) on tissue response to homeostatic signals and plasma variables associated with lipid metabolism in lactating dairy cows. Journal of Animal Science 80, 12851293.CrossRefGoogle ScholarPubMed
Baumgard, LH, Matitashvili, E, Corl, BA, Dwyer, DA & Bauman, DE (2001a). trans-10, cis-12 CLA decreases lipogenic rates and expression of genes involved in milk lipid synthesis in dairy cows. Journal of Dairy Science (In the Press).Google Scholar
Baumgard, LH, Sangster, JK & Bauman, DE (2001b) Milk fat synthesis is progressively reduced by increasing supplemental amounts of. trans-10, cis-12 conjugated linoleic acid (CLA).Journal of Nutrition 131, 17641769.CrossRefGoogle ScholarPubMed
Bee, G (2000) Dietary conjugated linoleic acid consumption during pregnancy and lactation influences growth and tissue composition in weaned pigs. Journal of Nutrition 130, 29812989.CrossRefGoogle ScholarPubMed
Boisclair, YR, Bauman, DE, Bell, AW, Dunshea, FR & Harkins, M (1994) Nutrient utilization and protein turnover in the hindlimb of cattle treated with bovine somatotropin. Journal of Nutrition 124, 664673.CrossRefGoogle ScholarPubMed
Chouinard, PY, Corneau, L, Barbano, DM, Metzger, LE & Bauman, DE (1999) Conjugated linoleic acids alter milk fatty acid composition and inhibit milk fat secretion in dairy cows. Journal of Nutrition 129, 15791584.CrossRefGoogle ScholarPubMed
DeLany, JP, Blohm, F, Truett, AA, Scimeca, JA & West, DB (1999) Conjugated linoleic acid rapidly reduces body fat content in mice without affecting energy intake. American Journal of Physiology 276, R1172R1179.Google ScholarPubMed
DeLany, JP & West, DB (2000) Changes in body composition with conjugated linoleic acid. Journal of American College of Nutrition 19, 487S493S.CrossRefGoogle ScholarPubMed
Dunshea, FR, Bauman, DE, Boyd, RD & Bell, AW (1992a) Temporal response of circulating metabolites and hormones during somatotropin treatment of growing pigs. Journal of Animal Science 70, 123131.CrossRefGoogle ScholarPubMed
Dunshea, FR, Boisclair, YR, Bauman, DE & Bell, AW (1995) Effects of bovine somatotropin and insulin on whole-body and hindlimb glucose metabolism in growing steers. Journal of Animal Science 73, 22632271.CrossRefGoogle ScholarPubMed
Dunshea, FR, Harris, DM, Bauman, DE, Boyd, RD & Bell, AW (1992b) Effect of porcine somatotropin on in vivo glucose kinetics and lipogenesis in growing pigs. Journal of Animal Science 70, 141151.CrossRefGoogle ScholarPubMed
Dunshea, FR, Harris, DM, Bauman, DE, Boyd, RD & Bell, AW (1992c) Effect of somatotropin on nonesterified fatty acid and glycerol metabolism in growing pigs. Journal of Animal Science 70, 132140.CrossRefGoogle ScholarPubMed
Dunshea, FR & King, RH (1994) Temporal response of plasma metabolites to ractopamine treatment in the growing pig. Australian Journal of Agricultural Research 45, 16831692.CrossRefGoogle Scholar
Dunshea, FR & King, RH (1995) Responses to homeostatic signals in ractopamine-treated pigs. British Journal of Nutrition 73, 809818.CrossRefGoogle ScholarPubMed
Harder, T, Rake, A, Rohde, W, Doerner, G & Plagemann, A (1999) Overweight and increased diabetes susceptibility in neonatally insulin-treated adult rats. Endocrine Regulations 33, 2531.Google ScholarPubMed
Houseknecht, KL, Vanden Heuvel, JP, Moya-Camarena, SY, Portocarrero, CP, Peck, LW, Nickel, KP & Belury, MA (1998) Dietary conjugated linoleic acid normalizes impaired glucose tolerance in the Zucker diabetic fatty fa/fa rat. Biochemical and Biophysical Research Communications 244, 678682.CrossRefGoogle ScholarPubMed
Johnson, MM & Peters, JP (1993) Technical note: an improved method to quantify nonesterified fatty acids in bovine plasma. Journal of Animal Science 71, 753756.CrossRefGoogle ScholarPubMed
Legro, RA, Finegood, D & Dunaif, A (1998) A fasting glucose to insulin ratio is a useful measure of insulin sensitivity in women with polycystic ovary syndrome. Journal of Clinical Endocrynology and Metabolism 83, 26942698.Google ScholarPubMed
O'Quinn, PR, Sith, JW, Nelssen, JL, Tokach, MD, Goodband, RD & Owen, KQ (1998) A comparison of modified tall oil and conjugated linoleic acid on growing–finishing pig growth performance and carcass characteristics. Journal of Animal Science 76, Suppl. 2, 61.Google Scholar
Ostrowska, E, Muralitharan, M, Cross, RF, Bauman, DE & Dunshea, FR (1999) Dietary conjugated linoleic acids increase lean tissue and decrease fat deposition in growing pigs. Journal of Nutrition 129, 20372042.CrossRefGoogle ScholarPubMed
Park, Y, Albright, KJ, Liu, W, Storkson, JM, Cook, ME & Pariza, MW (1997) Effect of conjugated linoleic acid on body composition in mice. Lipids 32, 853858.CrossRefGoogle ScholarPubMed
Park, Y, Albright, KJ, Storkson, JM, Liu, W, Cook, ME & Pariza, MW (1999a) Changes in body composition in mice during feeding and withdrawal of conjugated linoleic acid. Lipids 34, 243248.CrossRefGoogle ScholarPubMed
Park, Y, Storkson, JM, Albright, KJ, Liu, W & Pariza, MW (1999b) Evidence that the trans-10, cis-12 isomer of conjugated linoleic acid induces body composition changes in mice. Lipids 34, 235241.CrossRefGoogle ScholarPubMed
Payne, RW, Lane, PW and Genstat 5 Committee (1993). Genstat 5 Reference Manual. Oxford: Oxford Science Publications.CrossRefGoogle Scholar
Pethick, DW & Dunshea, FR (1993) Fat metabolism and turnover. In Aspects of Ruminant Digestion and Metabolism, pp. 291311. [Forbes, JM and France, J, editors]. Wallingford, Oxon: CAB International.Google Scholar
Ryder, JW, Portocarrero, CP, Song, XM, Cui, L, Yu, M, Combatsiaris, T, Galuska, D, Bauman, DE, Barbano, DM, Charron, MJ, Zierath, JR & Houseknecht, KL (2001) Isomer-specific antidiabetic properties of conjugated linoleic acid. Improved glucose tolerance, skeletal muscle insulin action, and UCP-2 gene expression. Diabetes 50, 11491157.CrossRefGoogle ScholarPubMed
Satory, DL & Smith, SB (1999) Conjugated linoleic acid inhibits proliferation but stimulates lipid filling of murine 3T3-L1 preadipocytes. Journal of Nutrition 129, 9297.CrossRefGoogle ScholarPubMed
Sechen, SJ, Dunshea, FR & Bauman, DE (1990) Somatotropin in lactating cows: effect on response to adrenaline and insulin. American Journal of Physiology 258, E582E588.Google ScholarPubMed
Stangl, GI, Muller, H & Kirchgessner, M (1999) Conjugated linoleic acid effects on circulating hormones, metabolites and lipoproteins, and its proportion in fasting serum and erythrocyte membranes of swine. European Journal of Nutrition 38, 271277.CrossRefGoogle ScholarPubMed
Tsuboyama-Kasaoka, N, Takahashi, M, Tanemura, K, Kim, HJ, Tange, T, Okuyama, H, Kasai, M, Ikemoto, S & Ezaki, O (2000) Conjugated linoleic acid supplementation reduces adipose tissue by apoptosis and develops lipodystrophy in mice. Diabetes 49, 15341542.CrossRefGoogle ScholarPubMed
West, DB, DeLany, JP, Camet, PM, Blohm, F, Truett, AA & Scimeca, J (1998) Effects of conjugated linoleic acid on body fat and energy metabolism in the mouse. American Journal of Physiology 275, R667R672.Google ScholarPubMed