Biochemical characterization and regional quantification of μ, δ and κ opioid binding sites in rat spinal cord

Craig Stevens, Carolyn B. Lacey, Kenneth Miller, Robert P. Elde, Virginia S. Seybold

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

The spinal cord contains μ, δ and κ opioid receptors which mediate the antinociceptive effects of opioid agonists administered onto the spinal cord. In this study, we characterized the binding sites for highly-selective μ, δ and κ opioid radioligands and quantified and distribution of opioid binding sites in rat lumbosacral spinal cord using autoradiography. In sections of rat brain mounted on glass slides, the μ ligand, [3H]sufentanil, bound with high affinity with an apparent Kd of 0.46 nM. The δ ligand, [3H]DPDPE ([d-Pen2,5]-enkephalin), bound with a Kd of 4.31 nM, and the κ-ligand, [3H]U69593, bound with a Kd of 2.27 nM. Three regions of the spinal gray were targeted for quantification of binding sites by autoradiography. The data indicate that when considered as a percentage of the total opioid binding capacity within a region, the contribution of μ sites in laminae I-II was about 90%, with δ and κ sites 7% and 3%, respectively. In lamina V, the μ sites comprised about 70% of the total opioid sites, with δ and κ sites comprising 28% and 2%, respectively. In the area adjacent to the central canal, μ sites contributed about 65% of the total opioid sites followed by δ sites at 33% and κ sites at 2% of total opioid sites. These results demonstrate a differential distribution of μ, δ and κ binding sites with respect to the organization of the spinal gray matter. The preferential occurrence of all 3 opioid binding sites in the superficial dorsal horn is noteworthy since many fine caliber primary afferent fibers mediating nociception establish synaptic contact in this region.

Original languageEnglish
Pages (from-to)77-85
Number of pages9
JournalBrain Research
Volume550
Issue number1
DOIs
StatePublished - 31 May 1991

Fingerprint

Opioid Analgesics
Spinal Cord
Binding Sites
Ligands
Autoradiography
D-Penicillamine (2,5)-Enkephalin
Sufentanil
Nociception
Enkephalins
Opioid Receptors
Glass
Brain

Keywords

  • Antinociception
  • Autoradiography
  • Dorsal horn
  • Opioid receptor
  • Pain pathway
  • Rat spinal cord

Cite this

Stevens, Craig ; Lacey, Carolyn B. ; Miller, Kenneth ; Elde, Robert P. ; Seybold, Virginia S. / Biochemical characterization and regional quantification of μ, δ and κ opioid binding sites in rat spinal cord. In: Brain Research. 1991 ; Vol. 550, No. 1. pp. 77-85.
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abstract = "The spinal cord contains μ, δ and κ opioid receptors which mediate the antinociceptive effects of opioid agonists administered onto the spinal cord. In this study, we characterized the binding sites for highly-selective μ, δ and κ opioid radioligands and quantified and distribution of opioid binding sites in rat lumbosacral spinal cord using autoradiography. In sections of rat brain mounted on glass slides, the μ ligand, [3H]sufentanil, bound with high affinity with an apparent Kd of 0.46 nM. The δ ligand, [3H]DPDPE ([d-Pen2,5]-enkephalin), bound with a Kd of 4.31 nM, and the κ-ligand, [3H]U69593, bound with a Kd of 2.27 nM. Three regions of the spinal gray were targeted for quantification of binding sites by autoradiography. The data indicate that when considered as a percentage of the total opioid binding capacity within a region, the contribution of μ sites in laminae I-II was about 90{\%}, with δ and κ sites 7{\%} and 3{\%}, respectively. In lamina V, the μ sites comprised about 70{\%} of the total opioid sites, with δ and κ sites comprising 28{\%} and 2{\%}, respectively. In the area adjacent to the central canal, μ sites contributed about 65{\%} of the total opioid sites followed by δ sites at 33{\%} and κ sites at 2{\%} of total opioid sites. These results demonstrate a differential distribution of μ, δ and κ binding sites with respect to the organization of the spinal gray matter. The preferential occurrence of all 3 opioid binding sites in the superficial dorsal horn is noteworthy since many fine caliber primary afferent fibers mediating nociception establish synaptic contact in this region.",
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Biochemical characterization and regional quantification of μ, δ and κ opioid binding sites in rat spinal cord. / Stevens, Craig; Lacey, Carolyn B.; Miller, Kenneth; Elde, Robert P.; Seybold, Virginia S.

In: Brain Research, Vol. 550, No. 1, 31.05.1991, p. 77-85.

Research output: Contribution to journalArticle

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