-
1
-
-
0031815337
-
Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: Evidence for agonist-directed trafficking of receptor stimulus
-
Berg KA, et al. (1998) Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: Evidence for agonist-directed trafficking of receptor stimulus. Mol Pharmacol 54:94-104.
-
(1998)
Mol Pharmacol
, vol.54
, pp. 94-104
-
-
Berg, K.A.1
-
2
-
-
41949089470
-
Beta-Arrestin-biased agonism at the beta2-adrenergic receptor
-
Drake MT, et al. (2008) beta-Arrestin-biased agonism at the beta2-adrenergic receptor. J Biol Chem 283:5669-5676.
-
(2008)
J Biol Chem
, vol.283
, pp. 5669-5676
-
-
Drake, M.T.1
-
3
-
-
45749146195
-
Conformational rearrangements and signaling cascades involved in ligand-biased mitogen-activated protein kinase signaling through the beta1-adrenergic receptor
-
Galandrin S, et al. (2008) Conformational rearrangements and signaling cascades involved in ligand-biased mitogen-activated protein kinase signaling through the beta1-adrenergic receptor. Mol Pharmacol 74:162-172.
-
(2008)
Mol Pharmacol
, vol.74
, pp. 162-172
-
-
Galandrin, S.1
-
4
-
-
33845903110
-
Functional selectivity and classical concepts of quantitative pharmacology
-
Urban JD, et al. (2007) Functional selectivity and classical concepts of quantitative pharmacology. J Pharmacol Exp Ther 320:1-13.
-
(2007)
J Pharmacol Exp Ther
, vol.320
, pp. 1-13
-
-
Urban, J.D.1
-
5
-
-
36348946976
-
Functional selectivity through protean and biased agonism: Who steers the ship?
-
Kenakin T (2007) Functional selectivity through protean and biased agonism: Who steers the ship? Mol Pharmacol 72:1393-1401.
-
(2007)
Mol Pharmacol
, vol.72
, pp. 1393-1401
-
-
Kenakin, T.1
-
6
-
-
35649027979
-
Long-acting kappa opioid antagonists disrupt receptor signaling and produce noncompetitive effects by activating c-Jun N-terminal kinase
-
Bruchas MR, et al. (2007) Long-acting kappa opioid antagonists disrupt receptor signaling and produce noncompetitive effects by activating c-Jun N-terminal kinase. J Biol Chem 282:29803-29811.
-
(2007)
J Biol Chem
, vol.282
, pp. 29803-29811
-
-
Bruchas, M.R.1
-
7
-
-
0033179904
-
Functional dissociation of mu opioid receptor signaling and endocytosis: Implications for the biology of opiate tolerance and addiction
-
Whistler JL, Chuang HH, Chu P, Jan LY, von Zastrow M (1999) Functional dissociation of mu opioid receptor signaling and endocytosis: Implications for the biology of opiate tolerance and addiction. Neuron 23:737-746.
-
(1999)
Neuron
, vol.23
, pp. 737-746
-
-
Whistler, J.L.1
Chuang, H.H.2
Chu, P.3
Jan, L.Y.4
Von Zastrow, M.5
-
8
-
-
0026764510
-
Extremely long-lasting antagonistic actions of nor-binaltorphimine (nor-BNI) in the mouse tail-flick test
-
Horan P, Taylor J, Yamamura HI, Porreca F (1992) Extremely long-lasting antagonistic actions of nor-binaltorphimine (nor-BNI) in the mouse tail-flick test. J Pharmacol Exp Ther 260:1237-1243.
-
(1992)
J Pharmacol Exp Ther
, vol.260
, pp. 1237-1243
-
-
Horan, P.1
Taylor, J.2
Yamamura, H.I.3
Porreca, F.4
-
9
-
-
0029054001
-
Opiate receptors
-
Reisine T (1995) Opiate receptors. Neuropharmacology 34:463-472.
-
(1995)
Neuropharmacology
, vol.34
, pp. 463-472
-
-
Reisine, T.1
-
10
-
-
0031726194
-
Agonist induced homologous desensitization of mu-opioid receptors mediated by G protein-coupled receptor kinases is dependent on agonist efficacy
-
Kovoor A, Celver JP, Wu A, Chavkin C (1998) Agonist induced homologous desensitization of mu-opioid receptors mediated by G protein-coupled receptor kinases is dependent on agonist efficacy. Mol Pharmacol 54:704-711.
-
(1998)
Mol Pharmacol
, vol.54
, pp. 704-711
-
-
Kovoor, A.1
Celver, J.P.2
Wu, A.3
Chavkin, C.4
-
11
-
-
0032499738
-
Role for G protein-coupled receptor kinase in agonist-specific regulation of mu-opioid receptor responsiveness
-
Zhang J, et al. (1998) Role for G protein-coupled receptor kinase in agonist-specific regulation of mu-opioid receptor responsiveness. Proc Natl Acad Sci USA 95: 7157-7162.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7157-7162
-
-
Zhang, J.1
-
12
-
-
46849091809
-
Morphine-induced mu-opioid receptor rapid desensitization is independent of receptor phosphorylation and beta-arrestins
-
Chu J, Zheng H, Loh HH, Law PY (2008) Morphine-induced mu-opioid receptor rapid desensitization is independent of receptor phosphorylation and beta-arrestins. Cell Signal 20:1616-1624.
-
(2008)
Cell Signal
, vol.20
, pp. 1616-1624
-
-
Chu, J.1
Zheng, H.2
Loh, H.H.3
Law, P.Y.4
-
13
-
-
0029778172
-
Morphine activates opioid receptors without causing their rapid internalization
-
Keith DE, et al. (1996) Morphine activates opioid receptors without causing their rapid internalization. J Biol Chem 271:19021-19024.
-
(1996)
J Biol Chem
, vol.271
, pp. 19021-19024
-
-
Keith, D.E.1
-
14
-
-
33746265800
-
Agonist-selective mechanisms of mu-opioid receptor desensitization in human embryonic kidney 293 cells
-
Johnson EA, et al. (2006) Agonist-selective mechanisms of mu-opioid receptor desensitization in human embryonic kidney 293 cells. Mol Pharmacol 70:676-685.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 676-685
-
-
Johnson, E.A.1
-
15
-
-
1242341368
-
G-protein receptor kinase 3 (GRK3) influences opioid analgesic tolerance but not opioid withdrawal
-
Terman GW, et al. (2004) G-protein receptor kinase 3 (GRK3) influences opioid analgesic tolerance but not opioid withdrawal. Br J Pharmacol 141:55-64.
-
(2004)
Br J Pharmacol
, vol.141
, pp. 55-64
-
-
Terman, G.W.1
-
16
-
-
0035923665
-
SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase
-
Bennett BL, et al. (2001) SP600125, an anthrapyrazolone inhibitor of Jun N-terminal kinase. Proc Natl Acad Sci USA 98:13681-13686.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 13681-13686
-
-
Bennett, B.L.1
-
17
-
-
0017064976
-
The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog
-
Martin WR, Eades CG, Thompson JA, Huppler RE, Gilbert PE (1976) The effects of morphine- and nalorphine- like drugs in the nondependent and morphine-dependent chronic spinal dog. J Pharmacol Exp Ther 197:517-532.
-
(1976)
J Pharmacol Exp Ther
, vol.197
, pp. 517-532
-
-
Martin, W.R.1
Eades, C.G.2
Thompson, J.A.3
Huppler, R.E.4
Gilbert, P.E.5
-
18
-
-
0026693403
-
Differential inhibition of hepatic morphine UDP-glucuronosyltransferases by metal ions
-
Lawrence AJ, Michalkiewicz A, Morley JS, MacKinnon K, Billington D (1992) Differential inhibition of hepatic morphine UDP-glucuronosyltransferases by metal ions. Biochem Pharmacol 43:2335-2340.
-
(1992)
Biochem Pharmacol
, vol.43
, pp. 2335-2340
-
-
Lawrence, A.J.1
Michalkiewicz, A.2
Morley, J.S.3
MacKinnon, K.4
Billington, D.5
-
19
-
-
0034054079
-
Ligand-induced changes in surface mu-opioid receptor number: Relationship to G protein activation?
-
Zaki PA, Keith DE, Jr, Brine GA, Carroll FI, Evans CJ (2000) Ligand-induced changes in surface mu-opioid receptor number: relationship to G protein activation? J Pharmacol Exp Ther 292:1127-1134.
-
(2000)
J Pharmacol Exp Ther
, vol.292
, pp. 1127-1134
-
-
Zaki, P.A.1
Keith Jr., D.E.2
Brine, G.A.3
Carroll, F.I.4
Evans, C.J.5
-
20
-
-
0038325573
-
Ligand-induced mu opioid receptor endocytosis and recycling in enteric neurons
-
Minnis JG, et al. (2003) Ligand-induced mu opioid receptor endocytosis and recycling in enteric neurons. Neuroscience 119:33-42.
-
(2003)
Neuroscience
, vol.119
, pp. 33-42
-
-
Minnis, J.G.1
-
21
-
-
2042527666
-
Effect of the A118G polymorphism on binding affinity, potency and agonist-mediated endocytosis, desensitization, and resensitization of the human mu-opioid receptor
-
Beyer A, Koch T, Schröder H, Schulz S, Höllt V (2004) Effect of the A118G polymorphism on binding affinity, potency and agonist-mediated endocytosis, desensitization, and resensitization of the human mu-opioid receptor. J Neurochem 89:553-560.
-
(2004)
J Neurochem
, vol.89
, pp. 553-560
-
-
Beyer, A.1
Koch, T.2
Schröder, H.3
Schulz, S.4
Höllt, V.5
-
22
-
-
1342265799
-
Distinct domains of the mu-opioid receptor control uncoupling and internalization
-
Celver J, Xu M, Jin W, Lowe J, Chavkin C (2004) Distinct domains of the mu-opioid receptor control uncoupling and internalization. Mol Pharmacol 65:528-537.
-
(2004)
Mol Pharmacol
, vol.65
, pp. 528-537
-
-
Celver, J.1
Xu, M.2
Jin, W.3
Lowe, J.4
Chavkin, C.5
-
23
-
-
52949125179
-
Differential activation and trafficking of micro-opioid receptors in brain slices
-
Arttamangkul S, et al. (2008) Differential activation and trafficking of micro-opioid receptors in brain slices. Mol Pharmacol 74:972-979.
-
(2008)
Mol Pharmacol
, vol.74
, pp. 972-979
-
-
Arttamangkul, S.1
-
24
-
-
77249125513
-
The effect of PKC and GRK inhibition on tolerance induced by mu opioid agonists of different efficacy
-
Hull LC, et al. (2010) The effect of PKC and GRK inhibition on tolerance induced by mu opioid agonists of different efficacy. J Pharmacol Exp Ther 332:1127-1135.
-
(2010)
J Pharmacol Exp Ther
, vol.332
, pp. 1127-1135
-
-
Hull, L.C.1
-
25
-
-
23944437411
-
Morphine promotes rapid, arrestin-dependent endocytosis of mu-opioid receptors in striatal neurons
-
Haberstock-Debic H, Kim KA, Yu YJ, von Zastrow M (2005) Morphine promotes rapid, arrestin-dependent endocytosis of mu-opioid receptors in striatal neurons. J Neurosci 25:7847-7857.
-
(2005)
J Neurosci
, vol.25
, pp. 7847-7857
-
-
Haberstock-Debic, H.1
Kim, K.A.2
Yu, Y.J.3
Von Zastrow, M.4
-
26
-
-
0029852678
-
Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene
-
Matthes HW, et al. (1996) Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene. Nature 383: 819-823.
-
(1996)
Nature
, vol.383
, pp. 819-823
-
-
Matthes, H.W.1
-
27
-
-
0037805628
-
Opioid agonists have different efficacy profiles for G protein activation, rapid desensitization, and endocytosis of mu-opioid receptors
-
Borgland SL, Connor M, Osborne PB, Furness JB, Christie MJ (2003) Opioid agonists have different efficacy profiles for G protein activation, rapid desensitization, and endocytosis of mu-opioid receptors. J Biol Chem 278:18776-18784.
-
(2003)
J Biol Chem
, vol.278
, pp. 18776-18784
-
-
Borgland, S.L.1
Connor, M.2
Osborne, P.B.3
Furness, J.B.4
Christie, M.J.5
-
28
-
-
0344780741
-
G-protein coupled receptor kinases as modulators of G-protein signalling
-
Bünemann M, Hosey MM (1999) G-protein coupled receptor kinases as modulators of G-protein signalling. J Physiol 517:5-23.
-
(1999)
J Physiol
, vol.517
, pp. 5-23
-
-
Bünemann, M.1
Hosey, M.M.2
-
29
-
-
0037013307
-
mu-Opioid receptors desensitize less rapidly than delta-opioid receptors due to less efficient activation of arrestin
-
Lowe JD, Celver JP, Gurevich VV, Chavkin C (2002) mu-Opioid receptors desensitize less rapidly than delta-opioid receptors due to less efficient activation of arrestin. J Biol Chem 277:15729-15735.
-
(2002)
J Biol Chem
, vol.277
, pp. 15729-15735
-
-
Lowe, J.D.1
Celver, J.P.2
Gurevich, V.V.3
Chavkin, C.4
-
30
-
-
33644938251
-
Comparison of the in vitro efficacy of mu, delta, kappa and ORL1 receptor agonists and non-selective opioid agonists in dog brain membranes
-
Lester PA, Traynor JR (2006) Comparison of the in vitro efficacy of mu, delta, kappa and ORL1 receptor agonists and non-selective opioid agonists in dog brain membranes. Brain Res 1073-1074:290-296.
-
(2006)
Brain Res
, vol.1073-1074
, pp. 290-296
-
-
Lester, P.A.1
Traynor, J.R.2
-
31
-
-
33644756719
-
Comparison of the antinociceptive response to morphine and morphine-like compounds in male and female Sprague-Dawley rats
-
Peckham EM, Traynor JR (2006) Comparison of the antinociceptive response to morphine and morphine-like compounds in male and female Sprague-Dawley rats. J Pharmacol Exp Ther 316:1195-1201.
-
(2006)
J Pharmacol Exp Ther
, vol.316
, pp. 1195-1201
-
-
Peckham, E.M.1
Traynor, J.R.2
-
32
-
-
63849297063
-
Two distinct mechanisms mediate acute muopioid receptor desensitization in native neurons
-
Dang VC, Napier IA, Christie MJ (2009) Two distinct mechanisms mediate acute muopioid receptor desensitization in native neurons. J Neurosci 29:3322-3327.
-
(2009)
J Neurosci
, vol.29
, pp. 3322-3327
-
-
Dang, V.C.1
Napier, I.A.2
Christie, M.J.3
-
33
-
-
33845653234
-
Uses for JNK: The many and varied substrates of the c-Jun N-terminal kinases
-
Bogoyevitch MA, Kobe B (2006) Uses for JNK: the many and varied substrates of the c-Jun N-terminal kinases. Microbiol Mol Biol Rev 70:1061-1095.
-
(2006)
Microbiol Mol Biol Rev
, vol.70
, pp. 1061-1095
-
-
Bogoyevitch, M.A.1
Kobe, B.2
-
34
-
-
1942423629
-
Phosphatidylinositol-3 kinase is distinctively required for mu-, but not kappa-opioid receptor-induced activation of c-Jun N-terminal kinase
-
Kam AY, Chan AS, Wong YH (2004) Phosphatidylinositol-3 kinase is distinctively required for mu-, but not kappa-opioid receptor-induced activation of c-Jun N-terminal kinase. J Neurochem 89:391-402.
-
(2004)
J Neurochem
, vol.89
, pp. 391-402
-
-
Kam, A.Y.1
Chan, A.S.2
Wong, Y.H.3
-
35
-
-
0033562607
-
Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization
-
Jin W, et al. (1999) Distinct domains of the CB1 cannabinoid receptor mediate desensitization and internalization. J Neurosci 19:3773-3780.
-
(1999)
J Neurosci
, vol.19
, pp. 3773-3780
-
-
Jin, W.1
-
36
-
-
38449115036
-
Role of receptor internalization in the agonist-induced desensitization of cannabinoid type 1 receptors
-
Wu DF, et al. (2008) Role of receptor internalization in the agonist-induced desensitization of cannabinoid type 1 receptors. J Neurochem 104:1132-1143.
-
(2008)
J Neurochem
, vol.104
, pp. 1132-1143
-
-
Wu, D.F.1
-
37
-
-
33748935747
-
Risperidone irreversibly binds to and inactivates the h5-HT7 serotonin receptor
-
Smith C, et al. (2006) Risperidone irreversibly binds to and inactivates the h5-HT7 serotonin receptor. Mol Pharmacol 70:1264-1270.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1264-1270
-
-
Smith, C.1
-
38
-
-
69549115130
-
Human 5-HT7 receptor-induced inactivation of forskolin-stimulated adenylate cyclase by risperidone, 9-OH-risperidone and other "inactivating antagonists"
-
Toohey N, Klein MT, Knight J, Smith C, Teitler M (2009) Human 5-HT7 receptor-induced inactivation of forskolin-stimulated adenylate cyclase by risperidone, 9-OH-risperidone and other "inactivating antagonists." Mol Pharmacol 76:552-559.
-
(2009)
Mol Pharmacol
, vol.76
, pp. 552-559
-
-
Toohey, N.1
Klein, M.T.2
Knight, J.3
Smith, C.4
Teitler, M.5
-
39
-
-
0033366394
-
Retention of heroin and morphine-6 beta-glucuronide analgesia in a new line of mice lacking exon 1 of MOR-1
-
Schuller AG, et al. (1999) Retention of heroin and morphine-6 beta-glucuronide analgesia in a new line of mice lacking exon 1 of MOR-1. Nat Neurosci 2:151-156.
-
(1999)
Nat Neurosci
, vol.2
, pp. 151-156
-
-
Schuller, A.G.1
-
40
-
-
77149154974
-
Phosphorylation of the mu-opioid receptor at tyrosine 166 (Tyr3.51) in the DRY motif reduces agonist efficacy
-
Clayton CC, Bruchas MR, Lee ML, Chavkin C (2010) Phosphorylation of the mu-opioid receptor at tyrosine 166 (Tyr3.51) in the DRY motif reduces agonist efficacy. Mol Pharmacol 77:339-347.
-
(2010)
Mol Pharmacol
, vol.77
, pp. 339-347
-
-
Clayton, C.C.1
Bruchas, M.R.2
Lee, M.L.3
Chavkin, C.4
|