Abstract

A heptadecapeptide was identified and purified from porcine brain tissue as a ligand for an orphan heterotrimeric GTP- binding protein (G protein)- coupled receptor (LC132) that is similar in sequence to opioid receptors. This peptide, orphanin FQ, has a primary structure reminiscent of that of opioid peptides. Nanomolar concentrations of orphanin FQ inhibited forskolin-stimulated adenylyl cyclase activity in cells transfected with LC132. This inhibitory activity was not affected by the addition of opioid ligands, nor did the peptide activate opioid receptors. Orphanin FQ bound to its receptor in a saturable manner and with high affinity. When injected intracerebroventricularly into mice, orphanin FQ caused a decrease in locomotor activity but did not induce analgesia in the hot-plate test. However, the peptide produced hyperalgesia in the tail-flick assay. Thus, orphanin FQ may act as a transmitter in the brain by modulating nociceptive and locomotor behavior.

Keywords

ChemistryNociceptin receptorAdenylyl cyclaseReceptorNeuropeptideOpioid receptorOpioid peptideOpioidHeterotrimeric G proteinPharmacologyG proteinHyperalgesiaInternal medicineNociceptionBiochemistryBiologyMedicine

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Publication Info

Year
1995
Type
article
Volume
270
Issue
5237
Pages
792-794
Citations
1812
Access
Closed

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Rainer K. Reinscheid, Hans‐Peter Nothacker, Anne Bourson et al. (1995). Orphanin FQ: A Neuropeptide That Activates an Opioidlike G Protein-Coupled Receptor. Science , 270 (5237) , 792-794. https://doi.org/10.1126/science.270.5237.792

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DOI
10.1126/science.270.5237.792