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The porcine mu opioid receptor: molecular cloning and mRNA distribution in lymphoid tissues

M S Pampusch1, M A Osinski, D R Brown

  • 1Department of Veterinary PathoBiology, University of Minnesota, St. Paul 55108, USA. pampu002@maroon.tc.umn.edu

Journal of Neuroimmunology
|November 17, 1998
PubMed

Insights

The porcine mu-opioid receptor (pMOR) is highly similar to the human version. Opioids may not directly suppress immune cells, but could indirectly modulate immune function via neuronal pMOR.

Area of Science:

  • Pharmacology
  • Immunology
  • Neuroscience

Background:

  • The mu-opioid receptor (MOR) plays a role in pain and reward pathways.
  • Opioid effects on the immune system are complex and not fully understood.
  • Previous research suggests potential interactions between opioids and immune cells.

Purpose of the Study:

  • To clone and characterize the porcine mu-opioid receptor (pMOR).
  • To investigate the distribution of pMOR mRNA in porcine tissues, including immune and non-immune tissues.
  • To determine if opioids directly impact immune cells via pMOR.

Main Methods:

  • Cloning of pMOR from porcine cerebral cortex RNA using Polymerase Chain Reaction (PCR).
  • Amino acid sequence comparison between porcine MOR and human MOR.
  • Reverse Transcription PCR (RT-PCR) to survey pMOR mRNA expression in various tissues.

Main Results:

  • Porcine MOR shares 96% amino acid identity with human MOR.
  • pMOR mRNA is widely distributed in the gut, thymus, and Peyer's patches.
  • pMOR mRNA was notably absent in other immune tissues and isolated immune cells.

Conclusions:

  • Opioids likely do not exert immunosuppressive effects through direct interaction with pMOR on immune cells.
  • Opioid modulation of immune function may occur indirectly through neuronal MOR in specific tissues.
  • Findings suggest a nuanced role for opioids in immune regulation, distinct from direct immune cell receptor interaction.

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