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Research Article

Modulation of Binding at Opioid Receptors by Monoand Divalent Cations and by Cholinergic Compounds

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Pages 363-373 | Published online: 26 Sep 2008

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Steven D. Stroop, Emma E. Moore, Rolf E. Kuestner & Deborah L. Thompson. (1993) Modulation of Calcitonin Binding by Calcium: Differential Effects of Divalent Cations. Journal of Receptor Research 13:8, pages 1173-1197.
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M.A. Ottinger, C. Corbitt, R. Hoffman, N. Thompson, E. Russek-Cohen & P. Deviche. (2006) Reproductive aging in Japanese quail, Coturnix japonica is associated with changes in central opioid receptors. Brain Research 1126:1, pages 167-175.
Crossref
Michael A. Statnick, Todd M. Suter, Susan L. Gackenheimer, Paul J. Emmerson, Steve J. Quimby, Donald R. Gehlert, William J. Wheeler & Charles H. Mitch. (2003) Na+-dependent high affinity binding of [3H]LY515300, a 3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid receptor inverse agonist. European Journal of Pharmacology 482:1-3, pages 139-150.
Crossref
George Rodgers, Cassandra Hubert, Jamie McKinzie, Todd Suter, Michael Statnick, Paul Emmerson & Louis Stancato. (2003) Development of Displacement Binding and GTPγS Scintillation Proximity Assays for the Identification of Antagonists of the μ-Opioid Receptor. ASSAY and Drug Development Technologies 1:5, pages 627-636.
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David Philippe, Laurent Dubuquoy, Hervé Groux, Valérie Brun, Myriam Tran Van Chuoï-Mariot, Claire Gaveriaux-Ruff, Jean-Frédéric Colombel, Brigitte L. Kieffer & Pierre Desreumaux. (2003) Anti-inflammatory properties of the μ opioid receptor support its use in the treatment of colon inflammation. Journal of Clinical Investigation 111:9, pages 1329-1338.
Crossref
Francesca Ceccarelli, Laura Giusti, Gianni Bigini, Barbara Costa, Dante Grillotti, Erika Fiumalbi, Antonio Lucacchini & Maria Rosa Mazzoni. (2001) Regulation of agonist binding to rat ETB receptors by cations and GTPγS11Abbreviations: ETs, endothelins; ETR, endothelin receptors; GTPγS, guanosine 5′-O-(2-thiotriphosphate); BQ 788, N-cis-2,6-dimethylpiperidinocarbonyl-l-γMeLeu-d-Trp(COOMe)-d-Nle-ONa; IRL 1620, suc-[Glu9, Ala11,15]-endothelin-1 (8-21); and PMSF, phenylmethanesulphonyl fluoride.. Biochemical Pharmacology 62:5, pages 537-545.
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E A Harper, N P Shankley & J W Black. (2009) Characterization of the binding of a novel radioligand to CCK B /gastrin receptors in membranes from rat cerebral cortex . British Journal of Pharmacology 126:6, pages 1504-1512.
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Cynthia C. Gulledge & Pierre Deviche. (1999) Age- and sex-related differences in opioid receptor densities in the songbird vocal control system. The Journal of Comparative Neurology 404:4, pages 505-514.
Crossref
Roger Bossé, Russell Garlick, Beverly Brown & Luc Ménard. (1998) Development of Nonseparation Binding and Functional Assays for G Protein-Coupled Receptors for High Throughput Screening: Pharmacological Characterization of the Immobilized CCR5 Receptor on FlashPlate®. SLAS Discovery 3:4, pages 285-292.
Crossref
V. Pliška. 1996. Lipophilicity in Drug Action and Toxicology. Lipophilicity in Drug Action and Toxicology 263 293 .
Cynthia C. Gulledge & Pierre Deviche. (2004) Autoradiographic localization of opioid receptors in vocal control regions of a male passerine bird ( Junco hyemalis ) . Journal of Comparative Neurology 356:3, pages 408-417.
Crossref
T. Reisine. (1995) Opiate receptors. Neuropharmacology 34:5, pages 463-472.
Crossref
B P Ceresa & L E Limbird. (1994) Mutation of an aspartate residue highly conserved among G-protein-coupled receptors results in nonreciprocal disruption of alpha 2-adrenergic receptor-G-protein interactions. A negative charge at amino acid residue 79 forecasts alpha 2A-adrenergic receptor sensitivity to allosteric modulation by monovalent cations and fully effective receptor/G-protein coupling.. Journal of Biological Chemistry 269:47, pages 29557-29564.
Crossref
Jin-Chung Chen, Emil R. Smith, Michael Cahill, Robert Cohen & Jordan B. Fishman. (1993) The opioid receptor binding of dezocine, morphine, fentanyl, butorphanol and nalbuphine. Life Sciences 52:4, pages 389-396.
Crossref
I. Ji & T.H. Ji. (1991) Asp383 in the second transmembrane domain of the lutropin receptor is important for high affinity hormone binding and cAMP production. Journal of Biological Chemistry 266:23, pages 14953-14957.
Crossref
Anna D. Ilyina, Sergei V. Zaitsev & Sergei D. Varfolomeyev. (1991) Kinetics of the dual-action mechanism of narcotic substances: conditions for conservative functioning of enzyme-receptor systems. Biosystems 25:3, pages 193-203.
Crossref
D A Horstman, S Brandon, A L Wilson, C A Guyer, E J CragoeJrJr & L E Limbird. (1990) An aspartate conserved among G-protein receptors confers allosteric regulation of alpha 2-adrenergic receptors by sodium.. Journal of Biological Chemistry 265:35, pages 21590-21595.
Crossref
Pierre Deviche, Thomas F. Murray & Frank L. Moore. (1990) Effects of sodium and temperature on naloxone binding in brain tissues of a urodele amphibian. Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 96:2, pages 393-398.
Crossref
P.J. Horan & I.K. Ho. (1989) Comparative pharmacological and biochemical studies between butorphanol and morphine. Pharmacology Biochemistry and Behavior 34:4, pages 847-854.
Crossref

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