Endogenous opioid peptides suppress cytokine-mediated upregulation of HIV-1 expression in the chronically infected promonocyte clone U1

Adv Exp Med Biol. 1995:373:65-72. doi: 10.1007/978-1-4615-1951-5_10.

Abstract

Opioid peptides appear to have an immunomodulatory activity. Using the chronically HIV-1-infected promonocyte clone U1, we investigated the effect of endogenous and synthetic opioid agonists on cytokine-induced HIV-1 expression. None of the endogenous or synthetic opioid agonists had an effect on constitutive HIV-1 expression. Opioid agonists such as methionine-enkephalin, dynorphin, and the kappa receptor agonist, U50,488, dose-dependently suppressed (> 40%) interleukin (IL)-6-induced upregulation of HIV-1 expression. Interestingly, opioid receptor antagonists (mu, delta, and kappa types) also inhibited (> 60%) IL-6-induced upregulation of HIV-1 expression. All opioid agonists and antagonists tested only modestly suppressed (< 20%) tumor necrosis factor-alpha-induced upregulation of HIV-1 expression in U1 cell cultures. These data suggest that certain opioid peptides alter an IL-6-induced signal transduction pathway which triggers HIV-1 expression in the chronically infected promonocyte U1.

Publication types

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

MeSH terms

  • Clone Cells
  • Cytokines / antagonists & inhibitors*
  • Cytokines / pharmacology
  • Endorphins / pharmacology*
  • Gene Expression Regulation, Viral / drug effects*
  • HIV-1 / drug effects
  • HIV-1 / genetics
  • HIV-1 / metabolism*
  • Humans
  • Monocytes / metabolism*
  • Monocytes / virology*
  • Receptors, Opioid / agonists
  • Signal Transduction / drug effects
  • Up-Regulation / drug effects*
  • Virus Replication / drug effects

Substances

  • Cytokines
  • Endorphins
  • Receptors, Opioid