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Effect of dietary rosemary extract on cell-mediated immunity of young rats

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Abstract

The impact of rosemary extract on splenic mononuclear cell proliferation was determined. Weanling male Sprague-Dawley rats were fed diets containing 0, 100, 200 or 400 ppm rosemary extract or 400 ppm butylated hydroxytoluene (BHT) in combinatiion with 10 or 20% casein enriched diets for 8 weeks. Splenic mononuclear cells were isolated from these animals and mitogenic response to Concanavalin A (Con A), Phytohemagglutinin (PHA) and lipopolysaccharide was determined. Con A and PHA-stimulated proliferation of spleen cells from rats fed 10% casein and 200 ppm rosemary extract was significantly higher than that of cells from the corresponding control animals. However, other levels of rosemary at 10% dietary casein or rosemary at any concentration fed along with 20% dietary casein had no impact on the mitogenic stimulation of splenic mononuclear cells. Thus, these results suggest that the use of rosemary might not have a generalized immunoenhancing effect, and will probably be effective in some stressed conditions, such as protein or antioxidant deficiency.

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References

  1. Aruoma OI, Haliwell B, Aeschbach R, Loligers J (1992) Antioxidant and pro-oxidant properties of active rosemary constituents: carnosol and carnosic acid. Xenobiotica 22: 257–268.

    Google Scholar 

  2. Kim SJ, Han D, Moon KD, Rhee JS (1995) Measurement of superoxide dismutase-like activity of natural antioxidants. Biosci Biotech Biochem 59(3): 822–826.

    Google Scholar 

  3. Paris A, Strukelj B, Renko M, Turk V (1993) Inhibitory effect of carnosolic acid on HIV-1 protease in cell-free assays. J Natural Products 56(8): 1426–1430.

    Google Scholar 

  4. Favier A, Sappey C, Leclerc P, Faure P, Micoud M (1994) Antioxidant status and lipid peroxidation in patients infected with HIV. Chemico-Biol Interact 91: 165–180.

    Google Scholar 

  5. Moriguchi S, Kobayashi N, Kishino Y (1990) High dietary intakes of vitamin E and cellular immune functions in rats. J Nutr 120: 1096–1102.

    Google Scholar 

  6. Meydani SN, Meydani M, Verdon CP, Shapiro AA, Blumberg JB, Hayes KC (1986) Vitamin E supplementation suppresses prostaglandin E2 synthesis and enhances the immune response of aged mice. Mech Ageing Develop 34: 191–201.

    Google Scholar 

  7. Meydani SN, Barklund MP, Liu S, Meydani M, Miller RA, Cannon JG, Morrow FD, Rocklin R, Blumberg JB (1990) Vitamin E supplementation enhances cell-mediated immunity in healthy elderly subjects. Am J Clin Nutr 52: 557–563.

    Google Scholar 

  8. Nash DR, Steingrube VA, Warrington RJ (1983) Primary immune responsiveness and other observations in mice given oral dimethyl sulfoxide. Immunopharmacology 6: 191–201.

    Google Scholar 

  9. Dornand J, Gerber M (1989) Inhibition of murine T-cell responses by anti-oxidants: the targets of lipo-oxygenase pathway inhibitors. Immunology 68: 384–391.

    Google Scholar 

  10. Huang C-J, Fwu M-L (1992) Protein insufficiency aggravates the enhanced lipid peroxidation and reduced activities of antioxidative enzymes in rats fed diets high in polyunsaturated fat. J Nutr 122: 1182–1189.

    Google Scholar 

  11. Yasunaga T, Kato H, Ohgaki K, Inamoto T, Hikasa Y (1982) Effect of vitamin E as an immunopotentiation agent for mice at optimal dosage and its toxicity at high dosage. J Nutr 112: 1075–1084.

    Google Scholar 

  12. Babu U, Failla ML (1989) Superoxide dismutase activity and blastogenic response of lymphocytes from copper-deficient rats fed diets containing fructose or corn starch. Nutr Res 9: 273–282.

    Google Scholar 

  13. Jenkins MY, Sheikh NM, Mitchell GV, Grundel E, Blakely SR, Carter CJ (1993) Dietary carotenoids influenced biochemical but not morphological changes in adult male rats fed a choline-deficient diet. Nutr Cancer 19: 55–65.

    Google Scholar 

  14. Ahmann GB, Sachs DH, Hodes RJ (1978) Requirement for an Ia-bearing accessory cell in Con A-induced T cell Proliferation. J Immunol 121(5): 1981–1989.

    Google Scholar 

  15. Droge W, Schulze-Osthoff K, Mihm S, Galter D, Schenk H, Eck HP, Roth S, Gmunder H (1994) Functions of glutathione and glutathione disulfide in immunology and immunopathology. Faseb J 8: 1131–1138.

    Google Scholar 

  16. Grimble RF (1997) Effect of antioxidative vitamins on immune function with clinical applications. Intern J Vit Nutr Res 67: 312–320.

    Google Scholar 

  17. Freed BM, Rapoport R, Lampert M (1987) Inhibition of early events in the human Tlymphocyte response to mitogens and alloantigens by hydrogen peroxide. Arch Surg 122: 99–104.

    Google Scholar 

  18. National Research Council (1978) Nutrient requirement of laboratory animals, 3rd edn, p. 23, Washington, DC: National Academy of Sciences.

    Google Scholar 

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Babu, U., Wiesenfeld, P. & Jenkins, M. Effect of dietary rosemary extract on cell-mediated immunity of young rats. Plant Foods Hum Nutr 53, 169–174 (1998). https://doi.org/10.1023/A:1008040324935

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  • DOI: https://doi.org/10.1023/A:1008040324935

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