Hostname: page-component-78c5997874-m6dg7 Total loading time: 0 Render date: 2024-11-20T03:37:44.921Z Has data issue: false hasContentIssue false

Dietary fat affects lipids and anti-cardiolipin antibody levels in autoimmune-prone NZB/W F1 mice

Published online by Cambridge University Press:  24 July 2007

Bi-Fong Lin
Affiliation:
Laboratory of Nutritional Chemistry, Department of Agricultural Chemistry, College of Agriculture, Taipei, Taiwan 10764, Republic of China
Su-Jen Jeng
Affiliation:
Laboratory of Nutritional Chemistry, Department of Agricultural Chemistry, College of Agriculture, Taipei, Taiwan 10764, Republic of China
Bor-Luen Chiang
Affiliation:
Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan 10764, Republic of China
Chao-Chi Huang
Affiliation:
Laboratory of Nutritional Chemistry, Department of Agricultural Chemistry, College of Agriculture, Taipei, Taiwan 10764, Republic of China
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.

Studies in autoimmune-prone NZB/W F1 mice have demonstrated that the amount of dietary fat can affect autoantibody production and the disease course of autoimmune diseases. Anti-cardiolipin antibodies have been found to play a major role in thrombus formation and the increase of abortion rate in both human lupus patients and murine lupus. The present study investigated further the effect of dietary fat on lipid and anti-cardiolipin antibody production in autoimmune-prone mice. Two groups of NZB/W F1 mice were fed on diets containing 200 g dietary fat/kg and 50 g dietary fat/kg respectively, the fat being composed of equal amounts of lard and soyabean oil. Serum levels of lipids, immunoglobulin (Ig) anti-single stranded DNA and anti-cardiolipin antibodies were followed regularly every month and mice were killed for in vitro experiments after 5 months on the experimental diets. The results showed that serum triacylglycerol concentration was lower in mice fed on the high-fat diet than in those fed on 50 g fat/kg. There was no significant difference in hepatic lipid contents; however, the fatty acid contents were different between these two groups. Hepatic linoleic acid (18:2n−6) and arachidonic acid (20:4n−6) concentrations were higher in mice fed on the high-fat diet. There were no significant differences in serum IgM concentrations or IgM anti-cardiolipin antibody levels between these two groups. However, IgG anti-cardiolipin antibody levels were higher in mice fed on the high-fat diet at the age of 3–4 months. Total serum IgG concentration was noted to be higher, but in contrast, serum IgA was lower, in the high-dietary-fat group. These findings suggest that high dietary fat may affect lipid metabolism and autoantibody levels in autoimmune diseases

Type
General Nutrition
Copyright
Copyright © The Nutrition Society 1997

References

REFERENCES

Berger, A., Gershwin, M. E. & German, J. B. (1992). Effects of various dietary fats on cardiolipin acyl composition during ontogeny of mice. Lipids 27, 605612.CrossRefGoogle ScholarPubMed
Carlson, S. E. & Goldfarb, S. (1979). A sensitive enzymatic method for the determination of free and esterified tissue cholesterol. Clinica Chimica Acta 79, 575582.CrossRefGoogle Scholar
Carroll, P., Stafford, D., Schwartz, R. S. & Stollar, B. D. (1985). Murine monoclonal anti-DNA autoantibodies bind to endogenous bacteria. Journal of Immunology 135, 10861090.CrossRefGoogle ScholarPubMed
Carteron, N. L., Schimenti, C. L. & Wofsy, D. (1989). Treatment of murine lupus with F(ab')2 fragments of monoclonal antibody to L3T4. Suppression of autoimmunity does not depend on T helper cell depletion. Journal of Immunology 142, 14701475.CrossRefGoogle Scholar
Datta, S. K., Patel, H. & Berry, D. (1987). Induction of cationic shift in IgG anti-DNA autoantibodies. Role of T helper cells with classical and novel phenotypes in three murine models of lupus nephritis. Journal of Experimental Medicine 165, 12521268.CrossRefGoogle ScholarPubMed
Eilat, D., Zlomick, A. Y. & Fischel, R. (1986). Evaluation of the cross-reaction between anti-DNA and anticardiolipin antibodies in SLE and experimental animals. Clinical Experimental Immunology 65, 269278.Google ScholarPubMed
Fernandes, G., Yunis, E. J. & Good, R. A. (1976). Influence of diet on survival of mice. Proceedings of the National Academy of Sciences USA 73, 12791283.CrossRefGoogle ScholarPubMed
Folch, J., Lees, M. & Sloane-Stanley, G. (1957). A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biological Chemistry 226, 497509.CrossRefGoogle ScholarPubMed
Fossati, P. & Prencipe, L. (1982). Serum triglycerides determined colonmetrically with an enzyme that produces hydrogen peroxide. Clinical Chemistry 28, 20772080.CrossRefGoogle ScholarPubMed
Gajjar, A., Kubo, C., Johnson, B. C. & Good, R. A. (1987). Influence of extremes of protein and energy intake on survival of B/W mice. Journal of Nutrition 117, 11361140.CrossRefGoogle ScholarPubMed
Haeeis, E. N., Gharavi, A. E., Patel, S. P. & Hughes, G. R. V. (1987). Evaluation of the anticardiolipin antibody test: report of an international workshop held April 1986. Clinical Experimental Immunology 68, 212215.Google Scholar
Harris, E. N., Gharavi, A. E., Boey, M. L., Patel, B. M., Mackworth-Young, C. G., Loizou, S. & Hughes, G. R. V. (1983). Anticardiolipin antibodies: detection by radioimmunoassay and association with thrombosis in systemic lupus erythematosus. Lancet 2, 12111214.CrossRefGoogle ScholarPubMed
Hashimoto, Y., Kawamura, M., Ichikawa, K., Suzuki, T., Sumida, T., Yoshida, S., Matsuura, E., Ikehara, S. & Koike, T. (1992). Anticardiolipin antibodies in NEW x BXSB F1 mice: a model of antiphospholipid syndrome. Journal of Immunology 149, 10631068.CrossRefGoogle Scholar
Hurd, E. T., Johnston, J. M, Okita, J. R., MacDonald, P. C., Ziff, M. & Gilliam, J. N. (1981). Prevention of glomerulonephritis and prolonged survival in New Zealand Black/New Zealand White F1 hybrid mice fed on essential fatty acid-deficient diet. Journal of Clinical Investigation 67, 476483.CrossRefGoogle ScholarPubMed
Koike, T., Sueishi, M., Funaki, H., Tomioka, H. & Yoshida, S. (1984). Antiphospholipid antibodies and biological false positive serological test for syphilis in patients with systemic lupus erythematosus. Clinical Experimental Immunology 56, 193199.Google ScholarPubMed
Koike, T., Tomioka, H. & Kumagai, A. (1982). Antibodies cross-reactive with DNA and cardiolipin in patients with systemic lupus erythematosus. Clinical Experimental Immunology 50, 298.Google ScholarPubMed
Kubo, C., Johnson, B. C., Day, N. K. & Good, R. A. (1984). Calorie source, calorie restriction, immunity and aging of (NZB/NEW) F1 mice. Journal of Nutrition 114, 18841899.CrossRefGoogle Scholar
Lafer, E. M., Raugh, J., Andrzejewski, C. Jr, Mudd, D., Furie, B., Schwarz, R. S. & Stollar, B. D. (1981). Polyspecific monoclonal lupus autoantibodies reactive with both polynuclmtides and phospholipids. Journal of Experimental Medicine 153, 897909.CrossRefGoogle ScholarPubMed
Lee, M.-H., Wang, M.-L. & Min, B.-W. (1990). Effects of methylation on determination of fatty acids. Food Science 17, 110.Google Scholar
Levy, J. A., Ibrahim, A. B., Shirai, T., Ohta, K., Nagasawa, R., Yoshida, H., Estes, J. & Gardner, M. (1982). Dietary fat affects immune response, production of antiviral factors, and immune complex disease in NZB/NZW mice. Proceedings of the Nationul Academy of Sciences USA 79, 19741978.CrossRefGoogle ScholarPubMed
Lin, B.-F., Huang, C.-C., Chiang, B.-L. & Jeng, S. -J. (1996). Dietary fat influences Ia antigen expression, cytokines and prostaglandin E2 production of immune cells in autoimmune-prone NZB x NZW F1 mice. British Journal of Nutrition 75, 711722.CrossRefGoogle ScholarPubMed
Lockshin, M. D., Druzin, M. L., Goei, S., Qamar, T., Magid, M. S., Janovic, L. & Ferenc, M. (1985). Antibody to cardiolipin as a predictor of fetal distress or death in pregnant patients with systemic lupus erythematosus. New England Journal of Medicine 313, 152156.CrossRefGoogle ScholarPubMed
MacGregor, A. J., Dhillon, V. B., Binder, A., Forte, C. A., Knight, B. C., Betterridge, D. J. & Isenberg, D. A. (1992). Fasting lipids and anticardiolipin antibodies as risk factors for vascular disease in systemic lupus erythematosus. Annals of Rheumatic Diseases 51, 152155.CrossRefGoogle ScholarPubMed
Mackworth-Young, C. (1990). Antiphospholipid antibodies: more than just a disease marker? Immunology Today 11, 6065.CrossRefGoogle ScholarPubMed
McNeil, H. P., Chesterman, C. N. & Krills, S. A. (1991). Immunology and clinical importance of antiphospholipid antibodies. Advances in Immunology 49, 193280.CrossRefGoogle ScholarPubMed
Morrow, W. J. W., Ohashi, Y., Hall, J., Pribnow, J., Hirose, S., Shirai, T. & Levy, J. A. (1985). Dietary fat and immune function. I. Antibody response, lymphocyte and accessory cell function in (NZB x NZW) F1 mice. Journal of Immunology 135, 38573863.CrossRefGoogle ScholarPubMed
National Research Council (1985). Guide for the Care and Use of Laboratory Animals. Publication no. 85–23 (revised). Bethesda, MD: National Institutes of Health.Google Scholar
Prickett, J. D., Robinson, D. R. & Steinberg, A. D. (1981). Dietary enrichment with the polyunsaturated fatty acid eicosapentaenoic acid prevents proteinuria and prolongs survival in NZB/W F1 mice. Journal of Clinical Investigation 68, 556559.CrossRefGoogle Scholar
Rauch, J., Tannenbaum, H., Stollar, B. D. & Schwartz, S. (1984). Monoclonal anti-cardiolipin antibodies bind to DNA. European Journal of Immunology 14, 529534.CrossRefGoogle ScholarPubMed
Richmond, N. (1973). Preparation and properties of a bacterial cholesterol oxidase from Nocardia sp. and its application to the enzymatic assay of total cholesterol in serum. Clinical Chemistry 19, 13501356.CrossRefGoogle Scholar
Rupin, A., Gruel, Y., Watier, H., Girard, A. C., Leroy, J. & Bardos, P. (1991). ELISA for the detection of anticardiolipin antibodies. High specificity based on the use of adult bovine serum as buffer and systematic subtraction of non-specific binding. Journal of Immunological Methods 138, 225231.CrossRefGoogle ScholarPubMed
Santoli, D. & Zurier, R. B. (1989). Prostaglandin E precursor fatty acids inhibit human IL-2 production by a prostaglandin E-independent mechanism. Journal of Immunology 143, 13031309.CrossRefGoogle ScholarPubMed
Shoenfeld, Y., Rauch, J., Massicotte, H., Datta, S. K., Andre-Schwartz, J., Stollar, B. D. & Schwartz, R. S. (1983). Polyspecificity of monoclonal lupus autoantibodies produced by human-human hybridomas. New England Journal of Medicine 308, 414420.CrossRefGoogle ScholarPubMed
Snyder, D. S., Beller, D. I. & Unanue, E. R. (1982). Prostaglandins modulate macrophage Ia expression. Nature 299, 163165.CrossRefGoogle ScholarPubMed
Steinberg, A. D., Huston, D. P., Taurog, J. D., Cowdery, J. S. & Raveche, E. S. (1981). The cellular and genetic basis of murine lupus. Immunology Review 55, 121154.CrossRefGoogle ScholarPubMed
Takeyama, M., Itoh, S., Nayasaki, T. & Tanimazu, I. (1977). A new enzymatic method for determinant of serum choline-containing phospholipids. Clinica Chimica Acta 79, 9398.Google Scholar
Theofilopoulos, A. N. & Dixon, F. J. (1981). Etiopathogenesis of murine SLE. Immunology Review 55, 179216.CrossRefGoogle ScholarPubMed
Theofilopoulos, A. N., Kofler, R., Singer, P. A. & Dixon, F. J. (1989). Molecular genetics of murine lupus models. Advances in Immunology 46, 61109.CrossRefGoogle ScholarPubMed