Suppression of adjuvant-induced disease (AID) by a novel analgesic-opioid agonist which also possesses antioxidant activity (neuroimmunomodulation)

Ann N Y Acad Sci. 1992 Apr 15:650:19-24. doi: 10.1111/j.1749-6632.1992.tb49089.x.

Abstract

A centrally acting analgesic-opioid agonist, PM, suppresses the primary inflammation and the secondary lesions of adjuvant-induced disease in rats. This compound also possesses antioxidant properties and inhibits the carrageenin-induced edema in mice. PM, therefore, is interfering to immune functions probably by binding to opioid receptors on lymphocytes and to inflammatory cells by its antioxidant activity.

MeSH terms

  • Analgesics / pharmacology*
  • Animals
  • Antioxidants / pharmacology*
  • Arthritis, Experimental / immunology*
  • Female
  • Lipid Peroxides / metabolism
  • Lymphocyte Activation / drug effects
  • Male
  • Morpholines / pharmacology*
  • Neuroimmunomodulation
  • Rats
  • Rats, Inbred F344

Substances

  • Analgesics
  • Antioxidants
  • Lipid Peroxides
  • Morpholines
  • 2-n-pentyloxy-2-phenyl-4-methylmorpholine