Nociceptin, Phe1 ψ-nociceptin1-13 , nocistatin and prepronociceptin154-181 effects on calcium channel currents and a potassium current in rat locus coeruleus in vitro

Author:

Connor Mark,Vaughan Christopher W,Jennings Ernest A,Allen Richard G,Christie Macdonald J

Publisher

Wiley

Subject

Pharmacology

Reference49 articles.

1. Nociceptin inhibits T-type Ca2+ channel current in rat sensory neurons by a G-protein-independent mechanism;ABDULLA;J. Neurosci.,1997

2. Assessment of the relative intrinsic activity of mu-opioid analgesics in vivo by using β-funaltrexamine;ADAMS;J. Pharmacol. Exp. Ther.,1990

3. Nociceptin (Orphanin FQ): high affinity and high capacity binding site coupled to low-potency stimulation of guanylyl-5′-O-(γ-thio)-triphosphate binding in rat brain membranes;ALBRECHT;J. Pharmacol. Exp. Ther.,1998

4. Orphanin-FQ/Nociceptin (OFQ/N) modulates the activity of suprachiasmatic nucleus neurons;ALLEN;J. Neurosci.,1999

5. Stimulation of guanosine-5′-O-(3-[35S]thio)triphosphate binding by endogenous opioids acting at a cloned mu receptor;ALT;J. Pharmacol. Exp. Ther.,1998

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