Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-25T02:49:45.743Z Has data issue: false hasContentIssue false

A comparison of the capacity of six cold-pressed plant oils to support development of acquired immune competence in the weanling mouse: superiority of low-linoleic-acid oils

Published online by Cambridge University Press:  09 March 2007

L. M. Hillyer
Affiliation:
Department of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON, CanadaN1G 2W1
Bill Woodward*
Affiliation:
Department of Human Biology and Nutritional Sciences, University of Guelph, Guelph, ON, CanadaN1G 2W1
*
*Corresponding author:Dr Bill Woodward, fax +1 519 763 5902, 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.

The objective of this investigation was to compare, at several levels of intake, the capacity of diverse cold-pressed plant oils to support development of acquired immune competence assessed in vivo in the weanling mouse. Safflower, maize, soyabean, rapeseed, flaxseed and olive oils were selected to represent widely differing 18: 1n-9, 18: 2n-6 and 18: 3n-3 contents, and each oil was fed at three dietary levels (40, 80 and 160 g/kg) as the exclusive source of fat. C57BL/6J mice, ten males and ten females, had free access to each diet for 28 d beginning at 19 d of age. The primary serum haemagglutinin response to sheep red blood cells and the primary cutaneous delayed hypersensitivity response to dinitrochlorobenzene were used to assess humoral and cell-mediated competence respectively, on day 28. A zero-time control group, assessed immunologically at 19 d of age, was also included (n 32). Independently of dietary oil level, flaxseed, rapeseed, olive and soyabean oils supported development of a more vigorous antibody response than safflower (a useful point of reference, being rich in 18: 2n-6 but low in 18: 1n-9 and 18: 3n-3), whereas only flaxseed oil supported development of cell-mediated responsiveness exceeding that of safflower-fed mice. Independently of oil type, development of both immunological indices correlated negatively with intake of 18: 2n-6, and development of humoral competence varied inversely with dietary oil level. A low content of 18: 2n-6, perhaps less than 20 g/100 g fatty acids, appears important to the capacity of a plant oil to support development of acquired immune competence in the young.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2002

References

Anonymous (1999) Fat and fresh: The best linseed oil. Proof! What Works in Alternative Medicine 10, 1113.Google Scholar
Beharka, AA, Wu, D, Han, SN & Meydani, SN (1997) Macrophage prostaglandin production contributes to the age-associated decrease in T cell function which is reversed by the dietary antioxidant vitamin E. Mechanisms of Ageing and Development 93, 5977.Google Scholar
Bemelmans, WJE, Broer, J, Feskens, EJM, Smit, AJ, Muskiet, FAJ, Lefrandt, JD, Bom, VJJ, May, JF & Meyboom-de Jong, B (2002) Effect of an increased intake of α-linolenic acid and group nutritional education on cardiovascular risk factors: the Mediterranean Alpha-linolenic Enriched Groningen Dietary Intervention (MARGARIN) study. American Journal of Clinical Nutrition 75, 221227.CrossRefGoogle ScholarPubMed
Bhatty, RS (1995) Nutrient composition of whole flaxseed and flaxseed meal. In Flaxseed in Human Nutrition, pp. 2242 [Cunnane, SC and Thompson, LU, editors]. Champaign, IL: AOCS Press.Google Scholar
Bierenbaum, ML, Reichstein, RP, Watkins, TR, Maginnis, WP & Geller, M (1991) Effects of canola oil on serum lipids in humans. Journal of the American College of Nutrition 10, 228233.Google Scholar
Bouic, PJD, Etsebeth, S, Liebenberg, RW, Albrecht, CF, Pegel, K & Van Jaarsveld, PP (1997) Beta-sitosterol and beta-sitosterol glucoside stimulate human peripheral blood lymphocyte proliferation: Implications for their use as an immunomodulatory vitamin combination. International Journal of Immunopharmacology 18, 693700.Google Scholar
Calder, PC (1998) Dietary fatty acids and the immune system. Nutrition Reviews 56, S70S83.Google Scholar
Calder, PC (2001) The effect of dietary fatty acids on the immune response and susceptibility to infection. In Nutrition, Immunity, and Infection in Infants and Children, pp. 137168 [Suskind, RM and Tontisirin, K, editors]. Philadelphia, PA: Vevey/Lippincott Williams & Wilkins.Google Scholar
Corsini, AC, Bellucci, SB & Costa, MG (1979) A simple method of evaluating delayed type hypersensitivity in mice. Journal of Immunological Methods 30, 195200.Google Scholar
Crevel, RWR, Friend, JV, Goodwin, BFJ & Parish, WE (1992) High-fat diets and the immune response of C57 Bl mice. British Journal of Nutrition 67, 1726.Google Scholar
Dearman, RJ, Moussavi, A, Kemeny, DM & Kimber, I (1996) Contribution of CD4+ and CD8+ T lymphocyte subsets to the cytokine secretion patterns induced in mice during sensitization to contact and respiratory chemical allergens. Immunology 89, 502510.CrossRefGoogle Scholar
DeFranco, AL (1999) B lymphocyte activation. In Fundamental Immunology, 4th ed., pp. 225261 [Paul, WE, editor]. Philadelphia, PA, New York, NY: Lippincott-Raven.Google Scholar
de Lorgeril, M, Renaud, S, Mamelle, N, Salen, P, Martin, JL, Monjaud, I, Guidollet, J, Touboul, P & Delaye, J (1994) Mediterranean alpha-linolenic acid-rich diet in secondary prevention of coronary heart disease. Lancet 343, 14541459.CrossRefGoogle ScholarPubMed
DeWille, JW, Fraker, PJ & Romsos, DR (1979) Effects of essential fatty acid deficiency and various levels of dietary polyunsaturated fatty acids on humoral immunity in mice. Journal of Nutrition 109, 10181022.Google Scholar
Erickson, KL, Adams, DA & Scibienski, RJ (1986) Dietary fatty acid modulation of murine B-cell responsiveness. Journal of Nutrition 116, 18301840.Google Scholar
Fritsche, KL, Cassity, NA & Huang, SC (1991) Effect of dietary fat source on antibody production and lymphocyte proliferation in chickens. Poultry Science 70, 611617.CrossRefGoogle ScholarPubMed
Fritsche, KL & Johnston, PV (1990) Effect of dietary omega-3 fatty acids on cell-mediated cytotoxic activity in BALB/C mice. Nutrition Research 10, 577588.Google Scholar
Hinds, A & Sanders, TAB (1993) The effect of increasing levels of dietary fish oil rich in eicosapentaenoic acid and docosahexaenoic acids on lymphocyte phospholipid fatty acid composition and cell-mediated immunity in the mouse. British Journal of Nutrition 69, 423429.CrossRefGoogle Scholar
Holub, BJ & Skeaff, CM (1987) Nutritional regulation of cellular phosphatidylinositol. Methods in Enzymology 141, 234244.CrossRefGoogle ScholarPubMed
Hosack-Fowler, K, Chapkin, RS & McMurray, DN (1993) Effects of purified dietary n-3 ethyl esters on murine T lymphocyte function. Journal of Immunology 151, 51865197.Google Scholar
Jeffery, NM, Sanderson, P, Sherrington, EJ, Newsholme, EA & Calder, PC (1996) The ratio of n-6 to n-3 polyunsaturated fatty acids in the rat diet alters serum lipid levels and lymphocyte functions. Lipids 31, 737745.CrossRefGoogle ScholarPubMed
Kelley, DS, Dougherty, RM, Branch, LB, Taylor, PC & Iacono, JM (1992) Concentration of dietary n-6 polyunsaturated fatty acids and human immune status. Clinical Immunology and Immunopathology 62, 240244.Google Scholar
Kelley, DS, Nelson, GJ, Serrato, CM, Schmidt, PC & Branch, LB (1988) Effect of type of dietary fat on indices of immune status of rabbits. Journal of Nutrition 118, 13761384.Google Scholar
Kolodziejczyk, PP & Fedec, P (1995) Processing flaxseed for human consumption. In Flaxseed in Human Nutrition, pp. 261280 [Cunnane, SC and Thompson, LU, editors]. Champaign, IL: AOCS Press.Google Scholar
Kris-Etherton, PM (1999) AHA science advisory: Monounsaturated fatty acids and risk of cardiovascular disease. Journal of Nutrition 129, 22802284.Google Scholar
Kris-Etherton, PM, Pearson, TA, Wan, Y, Hargrove, RL, Moriarty, K, Fishell, V & Etherton, TD (1999) High-monounsaturated fatty acid diets lower both plasma cholesterol and triacylglycerol concentrations. American Journal of Clinical Nutrition 70, 10091015.Google Scholar
Kuby, J (1997) Immunology, 3rd ed., New York, NY: WH Freeman and Company.Google Scholar
Larsen, LF, Jespersen, J & Marckmann, P (1999) Are olive oil diets anti-thrombotic? Diets enriched with olive, rapeseed, or sunflower oil affect postprandial factor VII differently. American Journal of Clinical Nutrition 70, 976982.Google Scholar
Leibson, HJ, Gefter, M, Zlotnik, A, Marrack, P & Kappler, JW (1984) Role of γ-interferon in antibody-producing responses. Nature 309, 799801.CrossRefGoogle ScholarPubMed
Litridou, M, Linssen, J, Schols, H, Bergmans, M, Pstrhumus, M, Tsimdou, M & Boskou, D (1997) Phenolic compounds in virgin olive oils: fractionation by solid-phase extraction and antioxidant activity assessment. Journal of the Science of Food and Agriculture 74, 169174.Google Scholar
Marshall, LA & Johnston, PV (1985) The influence of dietary essential fatty acids on rat immunocompetent cell prostaglandin synthesis and mitogen-induced blastogenesis. Journal of Nutrition 115, 15721580.CrossRefGoogle ScholarPubMed
Moreno, JJ, Carbonell, T, Sanchez, T, Miret, S & Mitjavila, MT (2001) Olive oil decreases both oxidative stress and the production of arachidonic acid metabolites by the prostaglandin G/H synthase pathway in rat macrophages. Journal of Nutrition 131, 21452149.Google Scholar
National Research Council (1995) Nutrient requirements of the mouse. In Nutrient Requirements of Laboratory Animals, pp. 80102. Washington, DC: National Academy Press.Google Scholar
Nelson, GJ & Chamberlain, JG (1995) The effect of dietary α-linolenic acid on blood lipids and lipoproteins in humans. In Flaxseed in Human Nutrition, pp. 187206 [Cunnane, SC and Thompson, LU, editors]. Champaign, IL: AOCS Press.Google Scholar
Ossmann, JB, Erickson, KL & Canolty, NL (1980) Effects of saturation and concentration of dietary fats on lymphocyte transformation in mice. Nutrition Reports International 22, 279284.Google Scholar
Poiley, SM (1972) Growth tables for 66 strains and stocks of laboratory animals. Laboratory Animal Science 22, 759799.Google Scholar
Reeves, PG, Nielsen, FH & Gahey, GC Jr (1993) AIN-93 purified diets of laboratory rodents: final report of the American Institute of Nutrition Ad Hoc Writing Committee on the reformation of the AIN-76 rodent diet. Journal of Nutrition 123, 19391951.Google Scholar
Robinson, LE & Field, CJ (1998) Dietary long-chain (n-3) fatty acids facilitate immune cell activation in sedentary, but not exercise-trained rats. Journal of Nutrition 128, 498504.CrossRefGoogle Scholar
Sanderson, P, Yaqoob, P & Calder, PC (1995 a) Effects of dietary lipid manipulation upon graft vs host and host vs graft responses in the rat. Cellular Immunololgy 164, 240247.Google Scholar
Sanderson, P, Yaqoob, P & Calder, PC (1995 b) Effects of dietary lipid manipulation upon rat spleen lymphocyte functions and the expression of lymphocyte surface molecules. Journal of Nutritional and Environmental Medicine 5, 119132.Google Scholar
Sell, S (1980) Cytotoxic or cytolytic reactions. In Immunology Immunopathology and Immunity, 3rd ed., pp. 226241New York, NY: Harper & Row.Google Scholar
Shipp, K & Woodward, BD (1998) A simple exsanguination method that minimizes acute pre-anesthesia stress in the mouse: Evidence based on serum corticosterone concentrations. Contemporary Topics in Laboratory Animal Science 37, 7377.Google ScholarPubMed
Shukla, VKS (1994) Present and future outlook of the world fats and oils supplies. In Technological Advances in Improved and Alternative Sources of Lipids, pp. 115 [Kamel, BS and Kakuda, Y, editors]. New York, NY: Blackie Academic and Professional.Google Scholar
Uceda, M & Hermoso, M (1997) La calidad del aceite de oliva. In El Cultivo del Olivo (Cultivation of the Olive), pp. 539564 [Barranco, D, Fernandez-Escobar, R and Rallo, L, editors]. Madrid: Junta de Andalucia & Ediciones Mundeprensa.Google Scholar
Woods, JW & Woodward, BD (1991) Enhancement of primary systemic acquired immunity by exogenous triiodothyronine in wasted, protein–energy malnourished weanling mice. Journal of Nutrition 121, 14251432.Google Scholar
Woodward, BD, Bezanson, KD, Hillyer, LM & Lee, W-H (1995) The CD45RA+ (quiescent) cellular phenotype is overabundant relative to the CD45RA- phenotype within the involuted splenic T cell population of weanling mice subjected to wasting protein–energy malnutrition. Journal of Nutrition 125, 24712482.Google Scholar