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Volumn 332, Issue 3, 2010, Pages 876-885

A hybrid indoloquinolizidine peptide as allosteric modulator of dopamine D1 receptors

Author keywords

[No Author keywords available]

Indexed keywords

2,3,4,5 TETRAHYDRO 7,8 DIHYDROXY 1 PHENYL 1H 3 BENZAZEPINE; 8 BROMO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL; 8 CHLORO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL HYDROGEN MALEATE; DOPAMINE 1 RECEPTOR STIMULATING AGENT; INDOLOQUINOLIZIDINE PEPTIDE 28; NEUROLEPTIC AGENT; UNCLASSIFIED DRUG;

EID: 77249153363     PISSN: 00223565     EISSN: 15210103     Source Type: Journal    
DOI: 10.1124/jpet.109.158824     Document Type: Article
Times cited : (14)

References (38)
  • 1
    • 0025878021 scopus 로고
    • Novel approaches to development of antipsychotics
    • Andersen PH and Nielsen EB (1991) Novel approaches to development of antipsychotics. Drug News Perspect 4:150-157.
    • (1991) Drug News Perspect , vol.4 , pp. 150-157
    • Andersen, P.H.1    Nielsen, E.B.2
  • 2
    • 34250359000 scopus 로고    scopus 로고
    • Dopamine receptors mRNA and protein expression in the mouse corpus striatum and cerebral cortex during pre- and post-natal development
    • Araki KY, Sims JR, and Bhide PG (2007) Dopamine receptors mRNA and protein expression in the mouse corpus striatum and cerebral cortex during pre- and post-natal development. Brain Res 1156:31-45.
    • (2007) Brain Res , vol.1156 , pp. 31-45
    • Araki, K.Y.1    Sims, J.R.2    Bhide, P.G.3
  • 3
    • 53449093828 scopus 로고    scopus 로고
    • G-protein-coupled receptors: From classical modes of modulation to allosteric mechanisms
    • Bridges TM and Lindsley CW (2008) G-protein-coupled receptors: from classical modes of modulation to allosteric mechanisms. ACS Chem Biol 3:530-541.
    • (2008) ACS Chem Biol , vol.3 , pp. 530-541
    • Bridges, T.M.1    Lindsley, C.W.2
  • 4
    • 69749126006 scopus 로고    scopus 로고
    • The effect of a full agonist/antagonist of the D1 receptor on locomotor activity, sensorimotor gating and cognitive function in dizocilpine-treated rats
    • Bubenikova-Valesova V, Svoboda J, Horacek J and Vales K (2009) The effect of a full agonist/antagonist of the D1 receptor on locomotor activity, sensorimotor gating and cognitive function in dizocilpine-treated rats. Int J Neuropsychopharmacol 12:873-883.
    • (2009) Int J Neuropsychopharmacol , vol.12 , pp. 873-883
    • Bubenikova-Valesova, V.1    Svoboda, J.2    Horacek, J.3    Vales, K.4
  • 5
    • 0030845192 scopus 로고    scopus 로고
    • Dose-dependent effects of the dopamine D1 receptor agonists A77636 or SKF81297 on spatial working memory in aged monkeys
    • Cai JX and Arnsten AF (1997) Dose-dependent effects of the dopamine D1 receptor agonists A77636 or SKF81297 on spatial working memory in aged monkeys. J Pharmacol Exp Ther 283:183-189.
    • (1997) J Pharmacol Exp Ther , vol.283 , pp. 183-189
    • Cai, J.X.1    Arnsten, A.F.2
  • 6
    • 0025194452 scopus 로고
    • Solubilization of A1 adenosine receptor from pig brain: Characterization and evidence of the role of the cell membrane on the coexistence of high- and low-affinity states
    • Casadó V, Cantí C, Mallol J, Canela EI, Lluis C, and Franco R (1990) Solubilization of A1 adenosine receptor from pig brain: characterization and evidence of the role of the cell membrane on the coexistence of high- and low-affinity states. J Neurosci Res 26:461-473.
    • (1990) J Neurosci Res , vol.26 , pp. 461-473
    • Casadó, V.1    Cantí, C.2    Mallol, J.3    Canela, E.I.4    Lluis, C.5    Franco, R.6
  • 7
    • 36249020990 scopus 로고    scopus 로고
    • Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: The receptordimer cooperativity index
    • Casadó V, Cortés A, Ciruela F, Mallol J, Ferré S, Lluis C, Canela EI, and Franco R (2007) Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: the receptordimer cooperativity index. Pharmacol Ther 116:343-354.
    • (2007) Pharmacol Ther , vol.116 , pp. 343-354
    • Casadó, V.1    Cortés, A.2    Ciruela, F.3    Mallol, J.4    Ferré, S.5    Lluis, C.6    Canela, E.I.7    Franco, R.8
  • 9
    • 70350044578 scopus 로고    scopus 로고
    • Useful pharmacological parameters for G-protein-coupled receptor homodimers obtained from competition experiments. Agonist-antagonist binding modulation
    • Casadó V, Ferrada C, Bonaventura J, Gracia E, Mallol J, Canela EI, Lluís C, Cortés A, and Franco R (2009b) Useful pharmacological parameters for G-protein-coupled receptor homodimers obtained from competition experiments. Agonist-antagonist binding modulation. Biochem Pharmacol 78:1456-1463.
    • (2009) Biochem Pharmacol , vol.78 , pp. 1456-1463
    • Casadó, V.1    Ferrada, C.2    Bonaventura, J.3    Gracia, E.4    Mallol, J.5    Canela, E.I.6    Lluís, C.7    Cortés, A.8    Franco, R.9
  • 10
    • 0036490942 scopus 로고    scopus 로고
    • Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery
    • Christopoulos A (2002) Allosteric binding sites on cell-surface receptors: novel targets for drug discovery. Nat Rev Drug Discov 1:198-210.
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 198-210
    • Christopoulos, A.1
  • 11
    • 58149193205 scopus 로고    scopus 로고
    • Allosteric modulators of GPCRs: A novel approach for the treatment of CNS disorders
    • Conn PJ, Christopoulos A, and Lindsley CW (2009) Allosteric modulators of GPCRs: a novel approach for the treatment of CNS disorders. Nat Rev Drug Discov 8:41-54.
    • (2009) Nat Rev Drug Discov , vol.8 , pp. 41-54
    • Conn, P.J.1    Christopoulos, A.2    Lindsley, C.W.3
  • 12
    • 59149087657 scopus 로고    scopus 로고
    • Ligand selectivity of D2 dopamine receptors is modulated by changes in local dynamics produced by sodium binding
    • Ericksen SS, Cummings DF, Weinstein H, and Schetz JA (2009) Ligand selectivity of D2 dopamine receptors is modulated by changes in local dynamics produced by sodium binding. J Pharmacol Exp Ther 328:40-54.
    • (2009) J Pharmacol Exp Ther , vol.328 , pp. 40-54
    • Ericksen, S.S.1    Cummings, D.F.2    Weinstein, H.3    Schetz, J.A.4
  • 16
    • 0032515074 scopus 로고    scopus 로고
    • A transmembrane domain-derived peptide inhibits D1 dopamine receptor function without affecting receptor oligomerization
    • George SR, Lee SP, Varghese G, Zeman PR, Seeman P, Ng GY, and O'Dowd BF (1998) A transmembrane domain-derived peptide inhibits D1 dopamine receptor function without affecting receptor oligomerization. J Biol Chem 273:30244-30248.
    • (1998) J Biol Chem , vol.273 , pp. 30244-30248
    • George, S.R.1    Lee, S.P.2    Varghese, G.3    Zeman, P.R.4    Seeman, P.5    Ng, G.Y.6    O'Dowd, B.F.7
  • 17
    • 0003534360 scopus 로고    scopus 로고
    • Paxinos G ed pp, Elsevier Academic Press, Amsterdam
    • Gerfen CR (2004) The Rat Nervous System (Paxinos G ed) pp 445-508, Elsevier Academic Press, Amsterdam.
    • (2004) The Rat Nervous System , pp. 445-508
    • Gerfen, C.R.1
  • 18
    • 0032802830 scopus 로고    scopus 로고
    • The physiological approach: Functional architecture of working memory and disordered cognition in schizophrenia
    • Goldman-Rakic PS (1999) The physiological approach: functional architecture of working memory and disordered cognition in schizophrenia. Biol Psychiatry 46: 650-661.
    • (1999) Biol Psychiatry , vol.46 , pp. 650-661
    • Goldman-Rakic, P.S.1
  • 20
    • 51049112029 scopus 로고    scopus 로고
    • Dopamine D2 receptors form higher order oligomers at physiological expression levels
    • Guo W, Urizar E, Kralikova M, Mobarec JC, Shi L, Filizola M, and Javitch JA (2008) Dopamine D2 receptors form higher order oligomers at physiological expression levels. EMBO J 27:2293-2304.
    • (2008) EMBO J , vol.27 , pp. 2293-2304
    • Guo, W.1    Urizar, E.2    Kralikova, M.3    Mobarec, J.C.4    Shi, L.5    Filizola, M.6    Javitch, J.A.7
  • 21
    • 69249158290 scopus 로고    scopus 로고
    • Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation
    • Han Y, Moreira IS, Urizar E, Weinstein H, and Javitch JA (2009) Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation. Nat Chem Biol 9:688-695.
    • (2009) Nat Chem Biol , vol.9 , pp. 688-695
    • Han, Y.1    Moreira, I.S.2    Urizar, E.3    Weinstein, H.4    Javitch, J.A.5
  • 22
    • 0033922586 scopus 로고    scopus 로고
    • Regulation of human D(1), d(2(long)), d(2(short)), D(3) and D(4) dopamine receptors by amiloride and amiloride analogues
    • Hoare SR, Coldwell MC, Armstrong D, and Strange PG (2000) Regulation of human D(1), d(2(long)), d(2(short)), D(3) and D(4) dopamine receptors by amiloride and amiloride analogues. Br J Pharmacol 130:1045-1059.
    • (2000) Br J Pharmacol , vol.130 , pp. 1045-1059
    • Hoare, S.R.1    Coldwell, M.C.2    Armstrong, D.3    Strange, P.G.4
  • 23
    • 33745257629 scopus 로고    scopus 로고
    • Agonist-induced cell surface trafficking of an intracellularly sequestered D1 dopamine receptor homo-oligomer
    • Kong MM, Fan T, Varghese G, O'Dowd BF, and George SR (2006) Agonist-induced cell surface trafficking of an intracellularly sequestered D1 dopamine receptor homo-oligomer. Mol Pharmacol 70:78-89.
    • (2006) Mol Pharmacol , vol.70 , pp. 78-89
    • Kong, M.M.1    Fan, T.2    Varghese, G.3    O'Dowd, B.F.4    George, S.R.5
  • 24
    • 0842265741 scopus 로고    scopus 로고
    • Layer V neurons bear the majority of mRNA encoding the five distinct dopamine receptors subtypes in the primate prefrontal cortex
    • Lidow MS, Wang F, Cao Y, and Goldman-Rakic PS (1998) Layer V neurons bear the majority of mRNA encoding the five distinct dopamine receptors subtypes in the primate prefrontal cortex. Synapse 28:10-20.
    • (1998) Synapse , vol.28 , pp. 10-20
    • Lidow, M.S.1    Wang, F.2    Cao, Y.3    Goldman-Rakic, P.S.4
  • 26
    • 12344326514 scopus 로고    scopus 로고
    • Treatments for schizophrenia: A critical review of pharmacology and mechanisms of action of antipsychotic drugs
    • Miyamoto S, Duncan GE, Marx CE, and Lieberman JA (2005) Treatments for schizophrenia: a critical review of pharmacology and mechanisms of action of antipsychotic drugs. Mol Psychiatry 10:79-104.
    • (2005) Mol Psychiatry , vol.10 , pp. 79-104
    • Miyamoto, S.1    Duncan, G.E.2    Marx, C.E.3    Lieberman, J.A.4
  • 27
    • 0345490945 scopus 로고    scopus 로고
    • Neubig RR, Spedding M, Kenakin T, Christopoulos A, and International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification (2003) International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology. Pharmacol Rev 55:597-606.
    • Neubig RR, Spedding M, Kenakin T, Christopoulos A, and International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification (2003) International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology. Pharmacol Rev 55:597-606.
  • 30
    • 0033944602 scopus 로고    scopus 로고
    • The heat shock cognate protein hsc73 assembles with A(1) adenosine receptors to form functional modules in the cell membrane
    • Sarrió S, Casadó V, Escriche M, Ciruela F, Mallol J, Canela EI, Lluis C, and Franco R (2000) The heat shock cognate protein hsc73 assembles with A(1) adenosine receptors to form functional modules in the cell membrane. Mol Cell Biol 20:5164-5174.
    • (2000) Mol Cell Biol , vol.20 , pp. 5164-5174
    • Sarrió, S.1    Casadó, V.2    Escriche, M.3    Ciruela, F.4    Mallol, J.5    Canela, E.I.6    Lluis, C.7    Franco, R.8
  • 31
    • 19944402189 scopus 로고    scopus 로고
    • Allosteric modulation of dopamine receptors
    • Schetz JA (2005) Allosteric modulation of dopamine receptors. Mini Rev Med Chem 5:555-561.
    • (2005) Mini Rev Med Chem , vol.5 , pp. 555-561
    • Schetz, J.A.1
  • 32
    • 0035144450 scopus 로고    scopus 로고
    • The binding-site crevice of the D4 dopamine receptor is coupled to three distinct sites of allosteric modulation
    • Schetz JA and Sibley DR (2001) The binding-site crevice of the D4 dopamine receptor is coupled to three distinct sites of allosteric modulation. J Pharmacol Exp Ther 296:359-363.
    • (2001) J Pharmacol Exp Ther , vol.296 , pp. 359-363
    • Schetz, J.A.1    Sibley, D.R.2
  • 33
    • 33645796458 scopus 로고    scopus 로고
    • Ago-allosteric modulation and other types of allostery in dimeric 7TM receptors
    • Schwartz TW and Holst B (2006) Ago-allosteric modulation and other types of allostery in dimeric 7TM receptors. J Recept Signal Transduct Res 26:107-128.
    • (2006) J Recept Signal Transduct Res , vol.26 , pp. 107-128
    • Schwartz, T.W.1    Holst, B.2
  • 34
    • 34447638166 scopus 로고    scopus 로고
    • Allosteric enhancers, allosteric agonists and agoallosteric modulators: Where do they bind and how do they act?
    • Schwartz TW and Holst B (2007) Allosteric enhancers, allosteric agonists and agoallosteric modulators: where do they bind and how do they act? Trends Pharmacol Sci 28:366-373.
    • (2007) Trends Pharmacol Sci , vol.28 , pp. 366-373
    • Schwartz, T.W.1    Holst, B.2
  • 38
    • 13444252378 scopus 로고    scopus 로고
    • Dopamine D1/D5 receptor antagonists with improved pharmacokinetics: Design, synthesis, and biological evaluation of phenol bioisosteric analogues of benzazepine D1/D5 antagonists
    • Wu WL, Burnett DA, Spring R, Greenlee WJ, Smith M, Favreau L, Fawzi A, Zhang H, and Lachowicz JE (2005) Dopamine D1/D5 receptor antagonists with improved pharmacokinetics: design, synthesis, and biological evaluation of phenol bioisosteric analogues of benzazepine D1/D5 antagonists. J Med Chem 48:680-693.
    • (2005) J Med Chem , vol.48 , pp. 680-693
    • Wu, W.L.1    Burnett, D.A.2    Spring, R.3    Greenlee, W.J.4    Smith, M.5    Favreau, L.6    Fawzi, A.7    Zhang, H.8    Lachowicz, J.E.9


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