Pain Forum
Volume 8, Issue 4 , Pages 206-209, Winter 1999

The Mu3 opiate receptor subtype

  • George B. Stefano

      Affiliations

    • Corresponding Author InformationReprint requests: George B. Stefano, PhD, Neuroscience Research Institute, State University of New York, College at Old Westbury, Old Westbury, NY 11568-0210.

Neuroscience Research Institute, State University of New York, College at Old Westbury, Old Westbury, New York

The mu3 opiate receptor subtype has been characterized by various binding assays as opiate alkaloid selective (eg, morphine) and opioid peptide (eg, methionine enkephalin) insensitive. The binding is monophasic, saturable, and stereospecific, as well as naloxone reversible. This opiate receptor subtype has been found on human and invertebrate tissues, demonstrating that it has been conserved during evolution. Furthermore, in numerous reports, this receptor is coupled to constitutive nitric oxide release. In this regard, for example, morphine immune downregulating activities parallels those actions formerly attributed to nitric oxide. Thus, this opiate receptor represents an addition to mu receptor heterogeneity that offers an explanation for the difference in actions of opioid peptides and opiate alkaloids in physiological systems transcending analgesia.

Key words: nitric oxide, morphine, opiate receptor, mu3 opiate receptor

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PII: S1082-3174(99)70010-3

doi:10.1016/S1082-3174(99)70010-3

Pain Forum
Volume 8, Issue 4 , Pages 206-209, Winter 1999