Human recombinant interferon alpha inhibits naloxone binding to rat brain membranes

Life Sci. 1992;50(24):PL227-32. doi: 10.1016/0024-3205(92)90555-4.

Abstract

Regulation of certain central nervous system (CNS) functions by the immune system may involve interferons (IFNs) acting through opioid receptors. Human recombinant interferon alpha (hrIFN alpha), as well as natural IFN alpha, have been reported to modulate a variety of physiological CNS functions both in vivo and in vitro. If the mechanism is via opioid receptors then IFN alpha should inhibit the binding of certain opioid radioligands to brain membranes. This study reports the inhibitory effect of hrIFN alpha on the binding of 3H-naloxone to rat brain membranes in vitro. The inhibitory effect at 37 degrees C is hrIFN alpha concentration dependent over the range of 500 to 6000 antiviral units per ml (U/ml) with 500 micrograms of membrane protein. The presence of NaCl (100mM) increases specific binding of naloxone and attenuates the inhibitory effect of hrIFN alpha. The inhibitory effect of hrIFN alpha is sensitive to temperature with maximum inhibition observed at 37 degrees C, and less as incubation temperature is reduced. These data suggest that IFN alpha may modulate certain physiologic functions via opioid pathways in the brain.

Publication types

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

MeSH terms

  • Animals
  • Brain / metabolism*
  • Humans
  • In Vitro Techniques
  • Interferon Type I / pharmacology*
  • Membranes / metabolism
  • Naloxone / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Opioid / drug effects
  • Recombinant Proteins
  • Serum Albumin, Bovine / pharmacology
  • Sodium Chloride / pharmacology
  • Temperature

Substances

  • Interferon Type I
  • Receptors, Opioid
  • Recombinant Proteins
  • Serum Albumin, Bovine
  • Naloxone
  • Sodium Chloride