Tolerance to Μ-opioid agonists in human neuroblastoma SH-SY5Y cells as determined by changes in guanosine-5′-O-(3-[ 35 S]-thio)triphosphate binding
dc.contributor.author | Elliott, Jackie | en_US |
dc.contributor.author | Guo, Li | en_US |
dc.contributor.author | Traynor, John R. | en_US |
dc.date.accessioned | 2010-06-01T18:30:54Z | |
dc.date.available | 2010-06-01T18:30:54Z | |
dc.date.issued | 1997-07 | en_US |
dc.identifier.citation | Elliott, Jackie; Guo, Li; Traynor, John R (1997). "Tolerance to Μ-opioid agonists in human neuroblastoma SH-SY5Y cells as determined by changes in guanosine-5′-O-(3-[ 35 S]-thio)triphosphate binding." British Journal of Pharmacology 121(7): 1422-1428. <http://hdl.handle.net/2027.42/71721> | en_US |
dc.identifier.issn | 0007-1188 | en_US |
dc.identifier.issn | 1476-5381 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/71721 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9257923&dopt=citation | en_US |
dc.format.extent | 381027 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | 1997 British Pharmacological Society | en_US |
dc.subject.other | Μ-Opioid Receptor Agonists | en_US |
dc.subject.other | Morphine | en_US |
dc.subject.other | DAMGO | en_US |
dc.subject.other | [ 35 S]-GTPΓS Binding | en_US |
dc.subject.other | Tolerance | en_US |
dc.subject.other | SH-SY5Y Cells | en_US |
dc.title | Tolerance to Μ-opioid agonists in human neuroblastoma SH-SY5Y cells as determined by changes in guanosine-5′-O-(3-[ 35 S]-thio)triphosphate binding | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Pharmacy and Pharmacology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, U.S.A. | en_US |
dc.identifier.pmid | 9257923 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/71721/1/sj.bjp.0701253.pdf | |
dc.identifier.doi | 10.1038/sj.bjp.0701253 | en_US |
dc.identifier.source | British Journal of Pharmacology | en_US |
dc.identifier.citedreference | Adams, J. & Holtzman, S.R. ( 1990 ). Tolerance and dependence after continuous morphine infusion from osmotic pumps measured by operant responding in rats. Psychopharmacology, 100, 451 – 458. | en_US |
dc.identifier.citedreference | Aloyo, V.J. ( 1995 ). Modulation of mu opioid binding by protein kinase inhibitors. Biochem. Pharmacol. 49, 17 – 21. | en_US |
dc.identifier.citedreference | Carroll, J.A., Shaw, J.S. & Wickenden, A.D. ( 1988 ). The physiological relevance of low agonist affinity binding at opioid Μ-receptors. Br. J. Pharmacol., 94, 625 – 631. | en_US |
dc.identifier.citedreference | Carter, B.D. & Medzihradsky, F. ( 1992 ). Opioid signal transduction in intact and fragmented SH-SY5Y neural cells. J. Neurochem., 58, 1611 – 1619. | en_US |
dc.identifier.citedreference | Carter, B.D. & Medzihradsky, F. ( 1993a ). Receptor mechanisms of opioid tolerance in SH-SY5Y human neural cells. Mol. Pharmacol., 43, 465 – 473. | en_US |
dc.identifier.citedreference | Carter, B.D. & Medzihradsky, F. ( 1993b ). Go mediates the coupling of Μ opioid receptor adenylyl cyclase in cloned neural cells and brain. Proc. Natl. Acad. Sci. U.S.A., 90, 4062 – 4066. | en_US |
dc.identifier.citedreference | Cheng, J., Standifer, K.M., Tublin, P.R., Su, W. & Pasternak, G.W. ( 1995 ). Demonstration of Κ 3 opioid receptors in the SH-SY5Y human neuroblastoma cell line. J. Neurochem., 65, 170 – 175. | en_US |
dc.identifier.citedreference | Cheng, Y.C. & Prussoff, W.H. ( 1973 ). Relationship between the inhibition constant (Ki) and the concentration of inhibitor which causes 50 per cent inhibition (150) of an enzymic reaction. Biochem. Pharmacol., 22, 3099 – 3108. | en_US |
dc.identifier.citedreference | Chidiac, P., Nouet, S. & Bouvier, M. ( 1996 ). Agonist-induced modulation of inverse agonist efficacy at the Β2-adrenergic receptor. Mol. Pharmacol., 50, 662 – 669. | en_US |
dc.identifier.citedreference | Childers, S.R. ( 1991 ). Opioid-receptor coupled 2nd messenger systems. Life Sci., 48, 1991 – 2002. | en_US |
dc.identifier.citedreference | Christie, M.J., Williams, J.T. & North, R.A. ( 1987 ). Cellular mechanisms of opioid tolerance: studies in single brain neurons. Mol. Pharmacol., 32, 633 – 638. | en_US |
dc.identifier.citedreference | Elliott, J., Lambert, D.G., Smart, D. & Traynor, J.R. ( 1994 ). Characterisation of Μ-opioid receptors on SH-SY5Y cells using naloxonazine and Β-funaltrexamine. Eur. J. Pharmacol. Mol. Pharmacol., 268, 447 – 450. | en_US |
dc.identifier.citedreference | Elliott, J. & Traynor, J.R. ( 1994 ). [ 35 S]GTPΓS binding in SH-SY5Y human neuroblastoma cells as a model for the study of opioid tolerance. Regul. Peptides, 54, 91 – 92. | en_US |
dc.identifier.citedreference | Hidaka, H., Inagaki, M., Kawamoto, S. & Sasaki, Y. ( 1984 ). Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide dependent kinase and protein kinase C. Biochemistry, 23, 5036 – 5041. | en_US |
dc.identifier.citedreference | Kazmi, S.M. & Mishra, R.K. ( 1987 ). Comparative pharmacological properties and functional coupling of Μ and Δ opioid receptor sites in human neuroblastoma SH-SY5Y cells. Mol. Pharmacol., 32, 109 – 118. | en_US |
dc.identifier.citedreference | Kennedy, C. & Henderson, G. ( 1991 ). Μ-Opioid receptor inhibition of calcium current: development of homologous tolerance in single SH-SY5Y cells after chronic exposure to morphine in vitro. Mol. Pharmacol., 40, 1000 – 1005. | en_US |
dc.identifier.citedreference | Kenakin, T. ( 1993 ). Pharmacologic Analysis of Drug-Receptor Interactions. 2nd edition, pp 249 – 277. New York: Raven Press. | en_US |
dc.identifier.citedreference | Lameh, J., Eiger, S. & Sadee, W. ( 1992 ). Interaction among Μ-opioid receptors and Α 2 -adrenoceptors on SH-SY5Y human neuroblastoma cells. Eur. J. Pharmacol., 227, 19 – 24. | en_US |
dc.identifier.citedreference | Laugwitz, K.-H., Offermanns, S., Spicher, K. & Schultz, G. ( 1993 ). Μ and Δ opioid receptors differentially couple to G protein subtypes in membranes of human neuroblastoma SH-SY5Y cells. Neuron, 10, 233 – 242. | en_US |
dc.identifier.citedreference | Lowry, O.H., Rosenberg, N.G., Farr, A.L. & Randall, R.J. ( 1951 ). Protein measurement with the Folin phenol reagent. J. Biol. Chem., 139, 265 – 275. | en_US |
dc.identifier.citedreference | Miller, S.W., Haske, T.N., Raby, C.A. & Levine, H. ( 1993 ). Inhibition of Β 2 adrenergic receptor desensitization. Soc. Neurosci Abs., 19, 181 – 5. | en_US |
dc.identifier.citedreference | Munson, P.J. & Rodbard, D. ( 1980 ). LIGAND: a versatile computerised approach for characterisation of ligand-binding systems. Anal. Biochem., 107, 220 – 239. | en_US |
dc.identifier.citedreference | Nestler, E.J. ( 1993 ). Cellular responses to chronic treatment with drugs of abuse. Critical Rev. Neurobiol., 7, 23 – 39. | en_US |
dc.identifier.citedreference | Pak, Y., Kouvelas, A., Scheideler, M.A., Rasmussen, J., O'Dowd, B.F. & George, S.R. ( 1996 ). Agonist-induced functional desensitization of the Μ- opioid receptor is mediated by loss of membrane receptors rather than uncoupling from G protein. Mol. Pharmacol. 50, 1214 – 1222. | en_US |
dc.identifier.citedreference | Pei, G., Keiffer, B.L., Lefkowitz, R.J. & Freedman, N.J. ( 1995 ). Agonist-dependent phosphorylation of the mouse Δ-opioid receptor: involvement of G-protein-coupled receptor kinases but not protein kinase C. Mol. Pharmacol., 48, 173 – 177. | en_US |
dc.identifier.citedreference | Prather, P.L., Tsai, A.W., & Law, P.Y. ( 1994 ). Mu and delta opioid receptor desensitization in undifferentiated human neuroblastoma cell SH-SY5Y cells. J. Pharmacol. Exp. Ther., 270, 177 – 184. | en_US |
dc.identifier.citedreference | Puttfarcken, P.S., Werling, L.L. & Cox, B.M. ( 1988 ). Effects of chronic morphine exposure on opioid inhibition of adenylyl cyclase in 7315c cell membranes: a useful model for the study of tolerance at Μ opioid receptors. Mol. Pharmacol., 33, 520 – 527. | en_US |
dc.identifier.citedreference | Raynor, K., Kong, H., Hines, J., Kong, G., Benovic, J., Yasuda, K., Bell, G. & Reisine, T. ( 1994 ). Molecular mechanisms of agonist-induced desensitization of the cloned mouse kappa opioid receptor. J. Pharmacol. Exp. Ther., 270, 1381 – 1386. | en_US |
dc.identifier.citedreference | Schiller, P.W., Nguyen, T.M.D., Weltowska, G., Wilkes, B.C., Marsden, B.C., Lemieux, C. & Chung, N.N. ( 1992 ). Differential stereochemical requirements of Μ versus Δ opioid receptors for ligand binding and signal transduction: development of a class of potent and highly Δ-selective peptide antagonists. Proc. Natl. Acad. Sci. U.S.A., 89, 11871 – 11875. | en_US |
dc.identifier.citedreference | Traynor, J.R. ( 1994 ). Opioid receptors and their subtypes: Focus on peripheral isolated tissue preparations. Neurochem. Int., 24, 427 – 432. | en_US |
dc.identifier.citedreference | Traynor, J.R. & Nahorski, S.R. ( 1995 ). Modulation by Μ-opioid agonists of guanosine-5′-O-(3-[ 35 S]thio)triphosphate binding to membranes from human neuroblastoma SH-SY5Y cells. Mol. Pharmacol., 47, 848 – 854. | en_US |
dc.identifier.citedreference | Traynor, J.R. & Wood, M.S. ( 1989 ). [ 3 H]Diprenorphine binding to kappa-sites in guinea-pig and rat brain: evidence for apparent heterogeneity. J. Neurochem., 53, 173 – 178. | en_US |
dc.identifier.citedreference | Ueda, H., Miyamea, T., Hayashi, C., Watanabe, S., Fukushima, N., Sasaki, Y., Iwamura, T. & Misu, Y. ( 1995 ). Protein kinase C involvement in homologous desensitization of the Δ-opioid receptor coupled to G il -phospholipase C activation in xenopus oocytes. J. Neurosci., 15, 7485 – 7499. | en_US |
dc.identifier.citedreference | Uhl, G.R., Childers, S. & Pasternak, G.W. ( 1993 ). An opiate-receptor gene family reunion. Trends Pharmacol. Sci., 17, 89 – 93. | en_US |
dc.identifier.citedreference | Van Vliet, B., Van Rijswijk, A.L.C.T., Wardeh, G., Mulder, A.H. & Schoffelmeer, A.N.M. ( 1993 ). Adaptive changes in the number of Gs- and Gi-proteins underlie adenylyl cyclase sensitization in morphine-treated rat striatal neurons. Eur. J. Pharmacol., 245, 23 – 29. | en_US |
dc.identifier.citedreference | Wang, Z., Bilsky, E.J., Porreca, F. & Sadee, W. ( 1994 ). Constitutive Μ opioid receptor activation as a regulatory mechanisms underlying narcotic tolerance and dependence. Life Sci., 54, 339 – 350. | en_US |
dc.identifier.citedreference | Yu, V.C. & Sadee, W. ( 1988 ). Efficacy and tolerance of narcotic analgesics at the mu opioid receptor in differentiated human neuroblastoma cells. J. Pharmacol. Exp. Ther., 245, 350 – 355. | en_US |
dc.identifier.citedreference | Zadina, J.E., Chang, S.L., Ge, L.-J. & Kastin, A.J. ( 1993 ). Mu opiate receptor down-regulation by morphine and up-regulation by naloxone in SH-SY5Y human neuroblastoma cells. J. Pharmacol. Exp. Ther., 265, 254 – 262. | en_US |
dc.identifier.citedreference | Zadina, J.E., Harrison, L.M., Ge, L.-J., Kastin, A.J. & Chang, S.L. ( 1994 ). Differential regulation of mu and delta opiate receptors by morphine, selective agonists and antagonists and differentiating agents in SH-SY5Y human neuroblastoma cells. J. Pharmacol. Exp. Ther., 270, 1086 – 1096. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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