[Phe1ψ(CH2‐NH)Gly2]nociceptin‐(1–13)‐NH2 activation of an inward rectifier as a partial agonist of O...
[Phe1ψ(CH2‐NH)Gly2]nociceptin‐(1–13)‐NH2 activation of an inward rectifier as a partial agonist of ORL1 receptors in rat periaqueductal gray
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Publisher
Oxford, UK: Blackwell Publishing Ltd
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Language
English
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Oxford, UK: Blackwell Publishing Ltd
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[Phe1ψ(CH2‐NH)Gly2]nociceptin‐(1–13)‐NH2 (Pheψ), a tridecapeptide analogue of orphanin FQ/nociceptin (OFQ/N), was introduced as a competitive antagonist of opioid receptor‐like orphan receptor (ORL1) in guinea‐pig ileum and mouse vas deferens preparations in vitro but was recently found to act as an agonist in vivo.
In the periaqueductal gray, a...
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Full title
[Phe1ψ(CH2‐NH)Gly2]nociceptin‐(1–13)‐NH2 activation of an inward rectifier as a partial agonist of ORL1 receptors in rat periaqueductal gray
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1571592
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1571592
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ISSN
0007-1188
E-ISSN
1476-5381
DOI
10.1038/sj.bjp.0702746