A delta2-opioid agonist inhibits p38 MAPK and suppresses activation of murine macrophages

J Surg Res. 2005 Sep;128(1):45-9. doi: 10.1016/j.jss.2005.04.003.

Abstract

Background: delta-Opioid agonists have been shown to attenuate ischemic organ injury in multiple models. The purpose of the present study was to determine if delta-opioid agonists could inhibit proinflammatory cytokine production by macrophages.

Material and methods: Murine macrophages (RAW 264.7) were pretreated for 4 h with media, a dose range (10(-4) to 10(-7) M) of DADLE ([D-Ala2], D-Leu5]-enkephalin, a nonspecific delta-opioid receptor agonist), a dose range (10(-4) to 10(-7) M) of DPDPE ([D2,5Pen]-enkephalin, a specific delta1-opioid receptor agonist), or a dose range (10(-4) to 10(-7) M) of Deltorphin-Dvariant (a specific delta2 opioid receptor agonist) and then incubated with 0.1 microg/ml lipopolysaccharide (LPS) for 1 or 4 h. Cytokine levels were measured by enzyme-linked immunosorbent assay. Activation of NF-kappaB, AP-1, and p38 MAPK were determined by mobility shift assays and Western blot.

Results: LPS induced significant increases in TNFalpha and MIP-2 production. Deltorphin-Dvariant, but not DADLE or DPDPE, dose-dependently reduced both TNFalpha and MIP-2 production. Deltorphin-Dvariant did not alter activation of the transcription factors NF-kappaB or AP-1, but greatly reduced activation of p38 MAPK.

Conclusions: The data show that delta2- but not delta1-opioid agonists suppress LPS-induced p38 MAPK activation and expression of TNFalpha and MIP-2.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • Cell Line
  • Chemokine CXCL2
  • Chemokines / biosynthesis
  • Cytokines / biosynthesis
  • Enkephalin, D-Penicillamine (2,5)- / pharmacology*
  • Enkephalin, Leucine-2-Alanine / pharmacology*
  • Lipopolysaccharides
  • Macrophage Activation / drug effects*
  • Macrophage Activation / immunology
  • Macrophages / drug effects
  • Macrophages / immunology
  • Mice
  • Oligopeptides / pharmacology*
  • Receptors, Opioid, delta / agonists
  • Tumor Necrosis Factor-alpha / biosynthesis
  • p38 Mitogen-Activated Protein Kinases / immunology

Substances

  • Analgesics, Opioid
  • Chemokine CXCL2
  • Chemokines
  • Cxcl2 protein, mouse
  • Cytokines
  • Lipopolysaccharides
  • Oligopeptides
  • Receptors, Opioid, delta
  • Tumor Necrosis Factor-alpha
  • deltorphin
  • Enkephalin, Leucine-2-Alanine
  • Enkephalin, D-Penicillamine (2,5)-
  • p38 Mitogen-Activated Protein Kinases