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Molecular Pharmacology

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Research ArticleArticle

Desensitization and tolerance of mu opioid receptors on pontine Kolliker-Fuse neurons.

Erica S. Levitt and John T. Williams
Molecular Pharmacology November 2, 2017, mol.117.109603; DOI: https://doi.org/10.1124/mol.117.109603
Erica S. Levitt
1 University of Florida;
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John T. Williams
2 Oregon Health & Science University
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Abstract

Acute desensitization of mu opioid receptors is thought to be an initial step in the development of tolerance to opioids. Given the resistance of the respiratory system to develop tolerance, desensitization of neurons in the Kölliker-Fuse (KF), a key area in the respiratory circuit, was examined. The activation of G protein-coupled inwardly rectifying potassium (GIRK) current was measured using whole-cell voltage-clamp recordings from KF and locus coeruleus (LC) neurons contained in acute rat brain slices. A saturating concentration of the opioid agonist [Met5]-enkephalin (ME) caused significantly less desensitization in KF neurons compared to LC neurons. In contrast to LC, desensitization in KF neurons was not enhanced by activation of PKC or in slices from morphine-treated rats. Cellular tolerance to ME and morphine was also lacking in KF neurons from morphine-treated rats. The lack of cellular tolerance in KF neurons correlates with the relative lack of tolerance to the respiratory depressant effect of opioids.

  • Desensitization/uncoupling
  • Gi family
  • Opioids
  • Patch clamp methods
  • Drug tolerance/dependence
  • The American Society for Pharmacology and Experimental Therapeutics
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Molecular Pharmacology: 103 (4)
Molecular Pharmacology
Vol. 103, Issue 4
1 Apr 2023
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Research ArticleArticle

Desensitization and tolerance of mu opioid receptors on pontine Kolliker-Fuse neurons.

Erica S. Levitt and John T. Williams
Molecular Pharmacology November 2, 2017, mol.117.109603; DOI: https://doi.org/10.1124/mol.117.109603

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Research ArticleArticle

Desensitization and tolerance of mu opioid receptors on pontine Kolliker-Fuse neurons.

Erica S. Levitt and John T. Williams
Molecular Pharmacology November 2, 2017, mol.117.109603; DOI: https://doi.org/10.1124/mol.117.109603
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