Mouse Strain Differences in in vivo and in vitro Immunosuppressive Effects of Opioids

  • Toby K. Eisenstein
  • Joseph J. MeisslerJr.
  • Jeanine L. Bussiere
  • Thomas J. Rogers
  • Ellen B. Geller
  • Martin W. Adler
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 373)

Abstract

We have previously demonstrated that subcutaneous (s.c.) implantation of a 75-mg morphine pellet in a variety of mouse strains (including C3HeB/FeJ, C3H/HeJ, C57BL/6ByJ, C57BL/6J bgJ/bgJ and C57BL/6J bgJ/+ [Beige homozygous and heterologous mice]) suppresses the primary in vitro plaque-forming cell (PFC) response to sheep red blood cells (SRBCs), when spleen cells are harvested 48 hours after drug administration (1, 2). Involvement of opioid receptors in the immunosuppression is shown by two observations: (i) simultaneous implantation of a naltrexone pellet blocks the morphine-induced immunosuppression in C3H lineage mice, and (ii) morphine does not suppress the CXBK/By mouse strain, which is deficient in μ opioid receptors (1). While this evidence clearly supports the involvement of classical opioid receptors in C3H lineage mice, these in vivo studies cannot rule out a role for the hypothalamic-pituitary-adrenal (HPA) axis or for other mediators from other systems participating in the observed immunosuppression (3–5).

Keywords

Placebo Lymphoma Morphine Adenosine Pyruvate 

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Copyright information

© Springer Science+Business Media New York 1995

Authors and Affiliations

  • Toby K. Eisenstein
    • 1
  • Joseph J. MeisslerJr.
    • 1
  • Jeanine L. Bussiere
    • 1
    • 2
  • Thomas J. Rogers
    • 1
  • Ellen B. Geller
    • 2
  • Martin W. Adler
    • 2
  1. 1.Department of Microbiology and ImmunologyUSA
  2. 2.Department of PharmacologyTemple University School of MedicinePhiladelphiaUSA

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