| Title | Activity of opioid ligands in cells expressing cloned mu opioid receptors. | | Author(s) | Gharagozlou P, Demirci H, David Clark J, Lameh J | | Institution | Department of Pharmacology, Molecular Research Institute, Mountain View, CA 94043, USA. parhamgr@purisima.molres.org | | Source | BMC Pharmacol 2003 Jan 4.:1. | | MeSH | Azocines
Binding, Competitive
Butorphanol
Cell Line
Comparative Study
Cyclic AMP
Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
Etorphine
Fentanyl
Forskolin
Humans
Hydromorphone
Ligands
Morphine
Naltrexone
Phenazocine
Radioligand Assay
Receptors, Opioid, mu
Research Support, U.S. Gov't, P.H.S.
Tritium
beta-Endorphin
| | Abstract | BACKGROUND: The aim of the present study was to describe the activity of a set of opioid drugs, including partial agonists, in a cell system expressing only mu opioid receptors. Receptor activation was assessed by measuring the inhibition of forskolin-stimulated cyclic adenosine mono phosphate (cAMP) production. Efficacies and potencies of these ligands were determined relative to the endogenous ligand beta-endorphin and the common mu agonist, morphine.
RESULTS: Among the ligands studied naltrexone, WIN 44,441 and SKF 10047, were classified as antagonists, while the remaining ligands were agonists. Agonist efficacy was assessed by determining the extent of inhibition of forskolin-stimulated cAMP production. The rank order of efficacy of the agonists was fentanyl = hydromorphone = beta-endorphin > etorphine = lofentanil = butorphanol = morphine = nalbuphine = nalorphine > cyclazocine = dezocine = metazocine >or= xorphanol. The rank order of potency of these ligands was different from that of their efficacies; etorphine > hydromorphone > dezocine > xorphanol = nalorphine = butorphanol = lofentanil > metazocine > nalbuphine > cyclazocine > fentanyl > morphine >>>> beta-endorphin.
CONCLUSION: These results elucidate the relative activities of a set of opioid ligands at mu opioid receptor and can serve as the initial step in a systematic study leading to understanding of the mode of action of opioid ligands at this receptor. Furthermore, these results can assist in understanding the physiological effect of many opioid ligands acting through mu opioid receptors. | | Language | eng | | Pub Type(s) | Journal Article
| | PubMed ID | 12513698 |
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