Enhanced oxygen metabolism of peritoneal macrophages in the presence of murine neuroblastoma cells is partly caused by enkephalins

J Neuroimmunol. 1988 Oct;19(4):269-78. doi: 10.1016/0165-5728(88)90008-2.

Abstract

A bioluminescent technique was used to show that murine neuroblastoma (NB) cells or cell-free extracts (H variant) were able to enhance the release of reactive oxygen intermediates (ROI) from peritoneal macrophages in vitro. L-variant NB cells were ineffective. Physiological concentrations of met-enkephalin produced the same effect in vitro but not leu-enkephalin. When both H- and L-variant cells, or their extracts, were incubated together with macrophages, ROI production was not increased. Similar findings were detectable when met- and leu-enkephalin were cultured together with macrophages. In vivo, preliminary studies gave the same results. The concentration rate of met- to leu-enkephalin was higher in H-variant than in L-variant NB cells. We conclude from our results that met-enkephalin can enhance the release of ROI from peritoneal macrophages. The difference in the effects produced by the H and L variants is due to differences in the concentrations of enkephalins released.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigenic Variation
  • Enkephalins / physiology*
  • Female
  • Macrophages / metabolism*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Neuroblastoma / analysis
  • Neuroblastoma / immunology
  • Neuroblastoma / pathology*
  • Oxygen Consumption* / drug effects
  • Peritoneal Cavity / cytology*
  • Tissue Extracts / pharmacology
  • Tumor Cells, Cultured

Substances

  • Enkephalins
  • Tissue Extracts