In vitro inhibition of histamine release from mouse mast cells and human basophils by an anthranilic acid derivative

Int J Immunopharmacol. 1983;5(5):431-5. doi: 10.1016/0192-0561(83)90019-x.

Abstract

Optimal conditions for in vitro histamine release mediated either by Con A (3 micrograms/ml) or by Ionophore A23187 (1 microgram/ml), were established for mouse peritoneal mast cells and human normal basophils. In both systems N-5' exerts potent inhibiting effects on histamine release after short term (1-5 minutes) in vitro preincubation. At concentrations of 1mM for mouse mast cells and 3mM for normal human basophils, N-5' inhibits up to 95% Con A-induced histamine release and more than 50% ionophore-induced histamine release. Such in vitro effects are more potent than DSCG-mediated inhibition, under similar experimental conditions, and are resistant to challenge with exceeding doses of the two releasing agents, particularly in the Con A system. Interestingly, basophils with apparent normal morphology, from a CML patient, were resistant to both challenges.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basophils / drug effects*
  • Calcimycin / pharmacology
  • Cells, Cultured
  • Concanavalin A / pharmacology
  • Histamine Release / drug effects*
  • Humans
  • Mast Cells / drug effects*
  • Mice
  • ortho-Aminobenzoates / pharmacology*

Substances

  • ortho-Aminobenzoates
  • Concanavalin A
  • Calcimycin
  • tranilast