Involvement of eicosanoids and macrophage-like cells in cytokine-mediated changes in rat myenteric nerves

Gastroenterology. 1995 Dec;109(6):1852-62. doi: 10.1016/0016-5085(95)90752-1.

Abstract

Background & aims: Proinflammatory cytokines alter function in enteric nerves, but little is known about underlying mechanisms. This study was designed to investigate the roles of prostanoids and of macrophage-like cells in cytokine-induced suppression of [3H]norepinephrine release from rat myenteric plexus.

Methods: The release of 3H from jejunal longitudinal muscle-myenteric plexus preparations that had been loaded with [3H]norepinephrine was measured. Measurements of 3H release as well as concentrations of prostaglandin E2 and leukotriene were made in preparations exposed to interleukin 1 beta plus interleukin 6 and in the presence or absence of piroxicam, 5-lipoxygenase inhibitor MK886, cycloheximide, or cyclosporin A. An ultrastructural analysis was also performed to investigate the presence of macrophage-like cells in the myenteric plexus.

Results: Interleukin 1 beta plus interleukin 6 suppressed 3H release and caused an increase in tissue prostaglandin E2 but not leukotriene E4. Piroxicam and cycloheximide but not MK886 attenuated the cytokine-induced increase in prostaglandin E2 and the suppression of [3H]norepinephrine release. Ultrastructural analysis showed macrophage-like cells in the plexus, and the cytokine effects were inhibited by cyclosporin A.

Conclusions: Prostanoids but not leukotrienes mediate the cytokine-induced suppression of norepinephrine release, and the results of this study suggest that macrophage-like cells are also involved.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Cycloheximide / pharmacology
  • Cyclooxygenase Inhibitors / pharmacology
  • Dinoprostone / biosynthesis
  • Dinoprostone / metabolism
  • Eicosanoids / metabolism*
  • Indoles / pharmacology
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / pharmacology*
  • Jejunum / innervation
  • Leukotrienes / biosynthesis
  • Leukotrienes / metabolism
  • Macrophages / physiology*
  • Macrophages / ultrastructure
  • Male
  • Muscle, Smooth / innervation
  • Myenteric Plexus / drug effects
  • Myenteric Plexus / metabolism*
  • Myenteric Plexus / ultrastructure
  • Norepinephrine / metabolism
  • Piroxicam / pharmacology
  • Protein Synthesis Inhibitors / pharmacology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Cyclooxygenase Inhibitors
  • Eicosanoids
  • Indoles
  • Interleukin-1
  • Interleukin-6
  • Leukotrienes
  • Protein Synthesis Inhibitors
  • MK-886
  • Piroxicam
  • Cycloheximide
  • Dinoprostone
  • Norepinephrine