• Title of article

    Opioid and nociceptin receptors regulate cytokine and cytokine receptor expression

  • Author/Authors

    Finley، نويسنده , , M.J. and Happel، نويسنده , , C.M. and Kaminsky، نويسنده , , D.E. and Rogers، نويسنده , , T.J.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2008
  • Pages
    9
  • From page
    146
  • To page
    154
  • Abstract
    Opioids were originally discovered because of their ability to induce analgesia, but further investigation has shown that the opioids regulate the function of cells involved in the immune response. We suggest that the regulation of cytokine, chemokine, and cytokine receptor expression is a critical component of the immunomodulatory activity of the opioids. In this paper we review the literature dealing with the regulation of cytokine and cytokine receptor expression by agonists for the three major opioid receptor types (μ, κ, and δ), and nociceptin, the natural agonist for the orphanin FQ/nociceptin receptor. Although the opioid receptors share a high degree of sequence homology, opposing roles between the kappa opioid receptor (KOR) and the mu opioid receptor (MOR) have become apparent. We suggest that activation of the KOR induces an anti-inflammatory response through the down-regulation of cytokine, chemokine and chemokine receptor expression, while activation of the MOR favors a pro-inflammatory response. Investigation into the opioid receptor-like (ORL1)/nociceptin system also suggests a role for this receptor as a down-regulator of immune function. These effects suggest a broad role for opioids in the modulation of the function of the immune system, and suggest possible targets for the development of new therapeutics for inflammatory and infectious diseases.
  • Keywords
    GPCR , ORL1 , HIV , Opioid , Chemokine , chemokine receptors , Opioid receptors , cytokine , Nociceptin
  • Journal title
    Cellular Immunology
  • Serial Year
    2008
  • Journal title
    Cellular Immunology
  • Record number

    1848252