메뉴 건너뛰기




Volumn 107, Issue 25, 2010, Pages 11608-11613

Ligand-directed c-Jun N-terminal kinase activation disrupts opioid receptor signaling

Author keywords

Acute analgesic tolerance; Biased agonism; Collateral agonist; Desensitization

Indexed keywords

ANTHRA[1,9 CD]PYRAZOL 6(2H) ONE; BUPRENORPHINE; ENKEPHALIN[2 DEXTRO ALANINE 4 METHYLPHENYLALANINE 5 GLYCINE]; FENTANYL; G PROTEIN COUPLED RECEPTOR; KAPPA OPIATE RECEPTOR; KAPPA OPIATE RECEPTOR AGONIST; METHADONE; MITOGEN ACTIVATED PROTEIN KINASE 10; MORPHINE; MORPHINE 6 GLUCURONIDE; MU OPIATE RECEPTOR; OPIATE RECEPTOR; OXYCODONE; PERTUSSIS TOXIN; ANALGESIC AGENT; LIGAND; MITOGEN ACTIVATED PROTEIN KINASE KINASE 4; NARCOTIC ANALGESIC AGENT; STRESS ACTIVATED PROTEIN KINASE;

EID: 77954923289     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1000751107     Document Type: Article
Times cited : (126)

References (40)
  • 1
    • 0031815337 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • Opiate receptors
    • Reisine T (1995) Opiate receptors. Neuropharmacology 34:463-472.
    • (1995) Neuropharmacology , vol.34 , pp. 463-472
    • Reisine, T.1
  • 10
    • 0031726194 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 19
    • 0034054079 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.