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Fish oil dietary supplementation reduces Ia expression in rat and mouse peritoneal macrophages.

Abstract
Preliminary studies suggest that administration of fish oil fatty acids may be beneficial in several immunological diseases; therefore, we studied the effect of fish oil dietary supplementation on the expression of Ia in stimulated murine peritoneal macrophages. Rats (n = 19) and mice (n = 27) on standard rodent feeding were separated in experimental (E) and control (C) groups that received fish oil or saline solution, respectively, daily for 4 weeks by esophageal gavage. Cholesterol serum levels were significantly lowered by fish oil (E vs C, P less than 0.01). E and C groups were injected intraperitoneally with Listeria monocytogenes (LM) and peritoneal cells were harvested 4 and 7 days after infection. Decreased expression of Ia induced by LM was found in rats (C = 49.68 +/- 5.09%, E = 16.95 +/- 4.3%, P less than 0.01) and mice (C = 47.38 +/- 7.63%, E = 26.66 +/- 1.92%, P less than 0.01). Animals with a more pronounced depression of serum cholesterol (reduction of 44.04 +/- 1.52% of baseline levels) had more depression of Ia expression (6.47 +/- 1.22%, P less than 0.001 vs control). Reduction of Ia expression was not related to PGE2 production by peritoneal cells. Reduction of Ia expression by fish oil could induce down-regulation of antigen presentation and alloreactivity.
AuthorsJ Mosquera, B Rodríguez-Iturbe, G Parra
JournalClinical immunology and immunopathology (Clin Immunol Immunopathol) Vol. 56 Issue 1 Pg. 124-9 (Jul 1990) ISSN: 0090-1229 [Print] United States
PMID2113444 (Publication Type: Journal Article)
Chemical References
  • Dietary Fats, Unsaturated
  • Fish Oils
  • Histocompatibility Antigens Class II
  • Dinoprostone
Topics
  • Animals
  • Dietary Fats, Unsaturated (pharmacology)
  • Dinoprostone (biosynthesis)
  • Fish Oils (pharmacology)
  • Gene Expression Regulation (drug effects)
  • Histocompatibility Antigens Class II (biosynthesis)
  • Listeria monocytogenes (immunology)
  • Macrophages (metabolism)
  • Male
  • Mice
  • Mice, Inbred C3H
  • Peritoneal Cavity (cytology)
  • Rats
  • Rats, Inbred Lew

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