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Inhibition of the accumulation of macrophages and the generation of macrophage chemotactic activity by dexamethasone in concanavalin A-induced peritonitis of mice.

Abstract
A delayed-type inflammatory response was evoked in mice using concanavalin A (Con A) as a stimulus, and the effect of various anti-inflammatory agents on the inflammation was examined. The intraperitoneal injection of Con A in the mouse resulted in the marked accumulation of leukocytes, especially macrophages, in the peritoneal cavity between 16 and 48 hr after the injection. Prior to the accumulation of macrophages, the chemotactic activity for macrophages appeared in the peritoneal fluid, and was associated with protein(s) in the molecular weight range from 10,000 to 100,000 daltons. When the effect of various agents on Con A-induced peritonitis was examined, neither anticomplementary agents (FUT-175 and K-76 COONa), bromophenacyl bromide, nordihydroguaiaretic acid nor indomethacin affected the generation of chemotactic activity and the accumulation of macrophages, suggesting that C5a, prostaglandins and leukotriene B4 are hardly involved in the Con A-induced macrophage accumulation. On the other hand, dexamethasone suppressed both the generation of chemotactic activity and the accumulation of macrophages. Taking into consideration the observation that the synthesis of macrophage chemotactic factors by mitogen-stimulated lymphocytes is inhibited by glucocorticoids, these results suggest that the macrophage chemotactic lymphokines might be involved in the accumulation of macrophages in Con A-induced peritonitis.
AuthorsI Nagaoka, H Kaneko, T Yamashita
JournalAgents and actions (Agents Actions) Vol. 25 Issue 1-2 Pg. 156-63 (Aug 1988) ISSN: 0065-4299 [Print] Switzerland
PMID3189042 (Publication Type: Journal Article)
Chemical References
  • Anti-Inflammatory Agents
  • Chemotactic Factors
  • Complement C5
  • Concanavalin A
  • Dexamethasone
  • Complement C5a
Topics
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Chemotactic Factors (biosynthesis)
  • Chemotaxis (drug effects)
  • Complement C5 (metabolism)
  • Complement C5a
  • Concanavalin A
  • Dexamethasone (pharmacology)
  • Kinetics
  • Macrophages (drug effects, immunology, pathology)
  • Male
  • Mice
  • Molecular Weight
  • Peritonitis (etiology, immunology, pathology)

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