메뉴 건너뛰기




Volumn 31, Issue 6, 2010, Pages 1194-1204

Pharmacological profile and antiparkinsonian properties of the novel nociceptin/orphanin FQ receptor antagonist 1-[1-cyclooctylmethyl-5-(1-hydroxy-1-methyl-ethyl)-1,2,3,6-tetrahydro-pyridin-4-yl]-3-ethyl-1,3-dihydro-benzoimidazol-2-one (GF-4)

Author keywords

6 Hydroxydopamine; GF 4; Microdialysis; Nociceptin orphanin FQ; NOP receptor knock out; Parkinson's disease

Indexed keywords

1 [1 CYCLOOCTYLMETHYL 5 (1 HYDROXY 1 METHYLETHYL) 1,2,3,6 TETRAHYDROPYRIDIN 4 YL] 3 ETHYL 1,3 DIHYDROBENZOIMIDAZOL 2 ONE; 4 AMINOBUTYRIC ACID; ANTIPARKINSON AGENT; GF 4; GLUTAMIC ACID; GLUTATHIONE; NOCICEPTIN RECEPTOR; NOCICEPTIN RECEPTOR ANTAGONIST; OPIATE RECEPTOR; UNCLASSIFIED DRUG;

EID: 77952102139     PISSN: 01969781     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.peptides.2010.03.015     Document Type: Article
Times cited : (16)

References (43)
  • 2
    • 33746573858 scopus 로고    scopus 로고
    • Differential protection against MPTP or metamphetamine toxicity in dopamine neurons by deletion of ppN/OFQ expression
    • Brown J.M., Gouty S., Iyer V., Rosenberger J., and Cox B.M. Differential protection against MPTP or metamphetamine toxicity in dopamine neurons by deletion of ppN/OFQ expression. J Neurochem 98 (2006) 495-505
    • (2006) J Neurochem , vol.98 , pp. 495-505
    • Brown, J.M.1    Gouty, S.2    Iyer, V.3    Rosenberger, J.4    Cox, B.M.5
  • 4
    • 0036015187 scopus 로고    scopus 로고
    • [Nphe1,Arg14,Lys15]nociceptin-NH2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptor
    • Calò G., Rizzi A., Rizzi D., Bigoni R., Guerrini R., Marzola G., et al. [Nphe1,Arg14,Lys15]nociceptin-NH2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptor. Br J Pharmacol 136 (2002) 303-311
    • (2002) Br J Pharmacol , vol.136 , pp. 303-311
    • Calò, G.1    Rizzi, A.2    Rizzi, D.3    Bigoni, R.4    Guerrini, R.5    Marzola, G.6
  • 5
    • 0015861774 scopus 로고
    • Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
    • Cheng Y., and Prusoff W.H. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 22 (1973) 3099-3108
    • (1973) Biochem Pharmacol , vol.22 , pp. 3099-3108
    • Cheng, Y.1    Prusoff, W.H.2
  • 6
    • 0035925579 scopus 로고    scopus 로고
    • Molecular cloning of the orphanin FQ receptor gene and differential tissue expression of splice variants in rat
    • Currò D., Yoo J.H., Anderson M., Song I., Del Valle J., and Owyang C. Molecular cloning of the orphanin FQ receptor gene and differential tissue expression of splice variants in rat. Gene 266 (2001) 139-145
    • (2001) Gene , vol.266 , pp. 139-145
    • Currò, D.1    Yoo, J.H.2    Anderson, M.3    Song, I.4    Del Valle, J.5    Owyang, C.6
  • 7
    • 0021998004 scopus 로고
    • Disinhibition as a basic process in the expression of striatal functions. II. The striato-nigral influence on thalamocortical cells of the ventromedial thalamic nucleus
    • Deniau J.M., and Chevalier G. Disinhibition as a basic process in the expression of striatal functions. II. The striato-nigral influence on thalamocortical cells of the ventromedial thalamic nucleus. Brain Res 334 (1985) 227-233
    • (1985) Brain Res , vol.334 , pp. 227-233
    • Deniau, J.M.1    Chevalier, G.2
  • 9
    • 67349192597 scopus 로고    scopus 로고
    • Pharmacological characterization of the nociceptin/orphanin FQ receptor nonpeptide antagonist Compound 24
    • Fischetti C., Camarda V., Rizzi A., Pelà M., Trapella C., Guerrini R., et al. Pharmacological characterization of the nociceptin/orphanin FQ receptor nonpeptide antagonist Compound 24. Eur J Pharmacol 614 (2009) 50-57
    • (2009) Eur J Pharmacol , vol.614 , pp. 50-57
    • Fischetti, C.1    Camarda, V.2    Rizzi, A.3    Pelà, M.4    Trapella, C.5    Guerrini, R.6
  • 10
    • 32344436732 scopus 로고    scopus 로고
    • Identification of a novel spiropiperidine opioid receptor-like 1 antagonist class by a focused library approach featuring 3D-pharmacophore similarity
    • Goto Y., Arai-Otsuki S., Tachibana Y., Ichikawa D., Ozaki S., Takahashi H., et al. Identification of a novel spiropiperidine opioid receptor-like 1 antagonist class by a focused library approach featuring 3D-pharmacophore similarity. J Med Chem 49 (2006) 847-849
    • (2006) J Med Chem , vol.49 , pp. 847-849
    • Goto, Y.1    Arai-Otsuki, S.2    Tachibana, Y.3    Ichikawa, D.4    Ozaki, S.5    Takahashi, H.6
  • 11
    • 0031006367 scopus 로고    scopus 로고
    • Address and message sequences for the nociceptin receptor: a structure-activity study of nociceptin-(1-13)-peptide amide
    • Guerrini R., Calò G., Rizzi A., Bianchi C., Lazarus L.H., Salvadori S., et al. Address and message sequences for the nociceptin receptor: a structure-activity study of nociceptin-(1-13)-peptide amide. J Med Chem 40 (1997) 1789-1793
    • (1997) J Med Chem , vol.40 , pp. 1789-1793
    • Guerrini, R.1    Calò, G.2    Rizzi, A.3    Bianchi, C.4    Lazarus, L.H.5    Salvadori, S.6
  • 13
    • 0347991783 scopus 로고    scopus 로고
    • Pharmacological profile of the cyclic nociceptin/orphanin FQ analogues c[Cys10,14]N/OFQ(1-14)NH2 and c[Nphe1,Cys10,14]N/OFQ(1-14)NH2
    • Kitayama M., Barnes T.A., Carra G., Calò G., Guerrini R., Rowbotham D.J., et al. Pharmacological profile of the cyclic nociceptin/orphanin FQ analogues c[Cys10,14]N/OFQ(1-14)NH2 and c[Nphe1,Cys10,14]N/OFQ(1-14)NH2. Naunyn Schmiedebergs Arch Pharmacol 368 (2003) 528-537
    • (2003) Naunyn Schmiedebergs Arch Pharmacol , vol.368 , pp. 528-537
    • Kitayama, M.1    Barnes, T.A.2    Carra, G.3    Calò, G.4    Guerrini, R.5    Rowbotham, D.J.6
  • 14
    • 0022980729 scopus 로고
    • Motor actions of excitatory amino acids and their antagonists within the rat ventromedial thalamic nucleus
    • Klockgether T., Turski L., Schwarz M., and Sontag K.H. Motor actions of excitatory amino acids and their antagonists within the rat ventromedial thalamic nucleus. Brain Res 399 (1986) 1-9
    • (1986) Brain Res , vol.399 , pp. 1-9
    • Klockgether, T.1    Turski, L.2    Schwarz, M.3    Sontag, K.H.4
  • 15
    • 0015372223 scopus 로고
    • Morphine catalepsy in the rat: relation to striatal dopamine metabolism
    • Kuschinsky K., and Hornykiewicz O. Morphine catalepsy in the rat: relation to striatal dopamine metabolism. Eur J Pharmacol 19 (1972) 119-122
    • (1972) Eur J Pharmacol , vol.19 , pp. 119-122
    • Kuschinsky, K.1    Hornykiewicz, O.2
  • 16
    • 48749095410 scopus 로고    scopus 로고
    • The nociceptin/orphanin FQ receptor: a target with broad therapeutic potential
    • Lambert D.G. The nociceptin/orphanin FQ receptor: a target with broad therapeutic potential. Nat Rev Drug Discov 7 (2008) 694-710
    • (2008) Nat Rev Drug Discov , vol.7 , pp. 694-710
    • Lambert, D.G.1
  • 18
    • 0037067112 scopus 로고    scopus 로고
    • Nociceptin/orphanin FQ receptors modulate glutamate extracellular levels in the substantia nigra pars reticulata. A microdialysis study in the awake freely moving rat
    • Marti M., Guerrini R., Beani L., Bianchi C., and Morari M. Nociceptin/orphanin FQ receptors modulate glutamate extracellular levels in the substantia nigra pars reticulata. A microdialysis study in the awake freely moving rat. Neuroscience 112 (2002) 153-160
    • (2002) Neuroscience , vol.112 , pp. 153-160
    • Marti, M.1    Guerrini, R.2    Beani, L.3    Bianchi, C.4    Morari, M.5
  • 19
    • 3342929522 scopus 로고    scopus 로고
    • Blockade of nociceptin/orphanin FQ receptor signaling in rat substantia nigra pars reticulate stimulates nigrostriatal dopaminergic transmission and motor behavior
    • Marti M., Mela F., Veronesi C., Guerrini R., Salvadori S., Federici M., et al. Blockade of nociceptin/orphanin FQ receptor signaling in rat substantia nigra pars reticulate stimulates nigrostriatal dopaminergic transmission and motor behavior. J Neurosci 24 (2004) 6659-6666
    • (2004) J Neurosci , vol.24 , pp. 6659-6666
    • Marti, M.1    Mela, F.2    Veronesi, C.3    Guerrini, R.4    Salvadori, S.5    Federici, M.6
  • 20
    • 10644257862 scopus 로고    scopus 로고
    • Blockade of nociceptin/orphanin FQ transmission in rat substantia nigra reverses haloperidol-induced akinesia and normalizes nigral glutamate release
    • Marti M., Mela F., Guerrini R., Calò G., Bianchi C., and Morari M. Blockade of nociceptin/orphanin FQ transmission in rat substantia nigra reverses haloperidol-induced akinesia and normalizes nigral glutamate release. J Neurochem 91 (2004) 1501-1504
    • (2004) J Neurochem , vol.91 , pp. 1501-1504
    • Marti, M.1    Mela, F.2    Guerrini, R.3    Calò, G.4    Bianchi, C.5    Morari, M.6
  • 21
    • 27144554951 scopus 로고    scopus 로고
    • Blockade of nociceptin/orphanin FQ transmission attenuates symptoms and neurodegeneration associated with Parkinson's disease
    • Marti M., Mela F., Fantin M., Witta J., Di Benedetto M., Buzas B., et al. Blockade of nociceptin/orphanin FQ transmission attenuates symptoms and neurodegeneration associated with Parkinson's disease. J Neurosci 95 (2005) 9591-9601
    • (2005) J Neurosci , vol.95 , pp. 9591-9601
    • Marti, M.1    Mela, F.2    Fantin, M.3    Witta, J.4    Di Benedetto, M.5    Buzas, B.6
  • 22
    • 33847003007 scopus 로고    scopus 로고
    • The nociceptin/orphanin FQ receptor antagonist J-113397 and l-DOPA additively attenuate experimental Parkinsonism through overinhibition of the nigrothalamic pathway
    • Marti M., Trapella C., Viaro R., and Morari M. The nociceptin/orphanin FQ receptor antagonist J-113397 and l-DOPA additively attenuate experimental Parkinsonism through overinhibition of the nigrothalamic pathway. J Neurosci 27 (2007) 1297-1307
    • (2007) J Neurosci , vol.27 , pp. 1297-1307
    • Marti, M.1    Trapella, C.2    Viaro, R.3    Morari, M.4
  • 23
    • 56749175350 scopus 로고    scopus 로고
    • The novel nociceptin/orphanin FQ receptor antagonist Trap-101 alleviates experimental parkinsonism through inhibition of the nigro-thalamic pathway: positive interaction with l-DOPA
    • Marti M., Trapella C., and Morari M. The novel nociceptin/orphanin FQ receptor antagonist Trap-101 alleviates experimental parkinsonism through inhibition of the nigro-thalamic pathway: positive interaction with l-DOPA. J Neurochem 107 (2008) 1683-1696
    • (2008) J Neurochem , vol.107 , pp. 1683-1696
    • Marti, M.1    Trapella, C.2    Morari, M.3
  • 24
    • 0000532368 scopus 로고
    • Evidence for a cyotchrome P-450 catalyzed allylic rearrangement with double bond topomerization
    • McClanahan R.H., Huitric A.C., Pearson P.G., Desper J.C., and Nelson S.D. Evidence for a cyotchrome P-450 catalyzed allylic rearrangement with double bond topomerization. J Am Chem Soc 110 (1988) 1979-1981
    • (1988) J Am Chem Soc , vol.110 , pp. 1979-1981
    • McClanahan, R.H.1    Huitric, A.C.2    Pearson, P.G.3    Desper, J.C.4    Nelson, S.D.5
  • 25
    • 12244301594 scopus 로고    scopus 로고
    • UFP-101, a high affinity antagonist for the nociceptin/orphanin FQ receptor: radioligand and GTPgamma(35)S binding studies
    • McDonald J., Calò G., Guerrini R., and Lambert D.G. UFP-101, a high affinity antagonist for the nociceptin/orphanin FQ receptor: radioligand and GTPgamma(35)S binding studies. Naunyn Schmiedebergs Arch Pharmacol 367 (2003) 183-187
    • (2003) Naunyn Schmiedebergs Arch Pharmacol , vol.367 , pp. 183-187
    • McDonald, J.1    Calò, G.2    Guerrini, R.3    Lambert, D.G.4
  • 26
    • 0037107156 scopus 로고    scopus 로고
    • Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections, linking multiple frontal cortical areas
    • McFarland N.R., and Haber S.N. Thalamic relay nuclei of the basal ganglia form both reciprocal and nonreciprocal cortical connections, linking multiple frontal cortical areas. J Neurosci 22 (2002) 8117-8132
    • (2002) J Neurosci , vol.22 , pp. 8117-8132
    • McFarland, N.R.1    Haber, S.N.2
  • 27
    • 0029166509 scopus 로고
    • Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor
    • Meunier J.C., Mollereau C., Toll L., Suaudeau C., Moisand C., Alvinerie P., et al. Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor. Nature 377 (1995) 532-535
    • (1995) Nature , vol.377 , pp. 532-535
    • Meunier, J.C.1    Mollereau, C.2    Toll, L.3    Suaudeau, C.4    Moisand, C.5    Alvinerie, P.6
  • 28
    • 0037128526 scopus 로고    scopus 로고
    • Nociceptin/orphanin FQ and opioid receptor-like receptor mRNA expression in dopamine systems
    • Norton C.S., Neal C.R., Kumar S., Akil H., and Watson S.J. Nociceptin/orphanin FQ and opioid receptor-like receptor mRNA expression in dopamine systems. J Comp Neurol 444 (2002) 358-368
    • (2002) J Comp Neurol , vol.444 , pp. 358-368
    • Norton, C.S.1    Neal, C.R.2    Kumar, S.3    Akil, H.4    Watson, S.J.5
  • 29
    • 0344224277 scopus 로고    scopus 로고
    • Effect of CGP 36742 on the extracellular level of neurotransmitter amino acids in the thalamus
    • Nyitrai G., Szàrics E., Kovàcs I., Kékesi K.A., Juhàsz G., and Kardos J. Effect of CGP 36742 on the extracellular level of neurotransmitter amino acids in the thalamus. Neurochem Int 34 (1999) 391-398
    • (1999) Neurochem Int , vol.34 , pp. 391-398
    • Nyitrai, G.1    Szàrics, E.2    Kovàcs, I.3    Kékesi, K.A.4    Juhàsz, G.5    Kardos, J.6
  • 30
    • 0034683206 scopus 로고    scopus 로고
    • In vitro and in vivo pharmacological characterization of J-113397, a potent and selective non-peptidyl ORL1 receptor antagonist
    • Ozaki S., Kawamoto H., Itoh Y., Miyagi M., Azuma T., Ichikawa D., et al. In vitro and in vivo pharmacological characterization of J-113397, a potent and selective non-peptidyl ORL1 receptor antagonist. Eur J Pharmacol 402 (2000) 45-53
    • (2000) Eur J Pharmacol , vol.402 , pp. 45-53
    • Ozaki, S.1    Kawamoto, H.2    Itoh, Y.3    Miyagi, M.4    Azuma, T.5    Ichikawa, D.6
  • 31
    • 0032508697 scopus 로고    scopus 로고
    • Identification and differential regional expression of KOR-3/ORL-1 gene splice variants in mouse brain
    • Pan Y.X., Xu J., Wan B.L., Zuckerman A., and Pasternak G.W. Identification and differential regional expression of KOR-3/ORL-1 gene splice variants in mouse brain. FEBS Lett 435 (1998) 65-68
    • (1998) FEBS Lett , vol.435 , pp. 65-68
    • Pan, Y.X.1    Xu, J.2    Wan, B.L.3    Zuckerman, A.4    Pasternak, G.W.5
  • 33
    • 0036201874 scopus 로고    scopus 로고
    • Nociceptin receptor antagonists display antidepressant-like properties in the mouse forced swimming test
    • Redrobe J.P., Calò G., Regoli D., and Quirion R. Nociceptin receptor antagonists display antidepressant-like properties in the mouse forced swimming test. Naunyn Schmiedebergs Arch Pharmacol 365 (2002) 164-167
    • (2002) Naunyn Schmiedebergs Arch Pharmacol , vol.365 , pp. 164-167
    • Redrobe, J.P.1    Calò, G.2    Regoli, D.3    Quirion, R.4
  • 35
    • 0031402010 scopus 로고    scopus 로고
    • An automated rotarod method for quantitative drug-free evaluation of overall motor deficits in rat models of parkinsonism
    • Rozas G., Guerra M.J., and Labandeira-Garcia J.L. An automated rotarod method for quantitative drug-free evaluation of overall motor deficits in rat models of parkinsonism. Brain Res Brain Res Protoc 2 (1997) 75-84
    • (1997) Brain Res Brain Res Protoc , vol.2 , pp. 75-84
    • Rozas, G.1    Guerra, M.J.2    Labandeira-Garcia, J.L.3
  • 36
    • 0018421663 scopus 로고
    • Excessive bracing reactions and their control by atropine and l-DOPA in an animal analog of parkinsonism
    • Schallert T., De Ryck M., Whishaw I.Q., Ramirez V.D., and Teitelbaum P. Excessive bracing reactions and their control by atropine and l-DOPA in an animal analog of parkinsonism. Exp Neurol 64 (1979) 33-43
    • (1979) Exp Neurol , vol.64 , pp. 33-43
    • Schallert, T.1    De Ryck, M.2    Whishaw, I.Q.3    Ramirez, V.D.4    Teitelbaum, P.5
  • 37
    • 0034736150 scopus 로고    scopus 로고
    • 4-Aminoquinolines: novel nociceptin antagonists with analgesic activity
    • Shinkai H., Ito T., Iida T., Kitao Y., Yamada H., and Uchida I. 4-Aminoquinolines: novel nociceptin antagonists with analgesic activity. J Med Chem 43 (2000) 4667-4677
    • (2000) J Med Chem , vol.43 , pp. 4667-4677
    • Shinkai, H.1    Ito, T.2    Iida, T.3    Kitao, Y.4    Yamada, H.5    Uchida, I.6
  • 38
    • 34248525042 scopus 로고    scopus 로고
    • Pharmacological characterization of the nociceptin/orphanin FQ receptor antagonist SB-612111 [(-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol]: in vitro studies
    • Spagnolo B., Carrà G., Fantin M., Fischetti C., Hebbes C., McDonald J., et al. Pharmacological characterization of the nociceptin/orphanin FQ receptor antagonist SB-612111 [(-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol]: in vitro studies. J Pharmacol Exp Ther 321 (2007) 961-967
    • (2007) J Pharmacol Exp Ther , vol.321 , pp. 961-967
    • Spagnolo, B.1    Carrà, G.2    Fantin, M.3    Fischetti, C.4    Hebbes, C.5    McDonald, J.6
  • 39
    • 28844466468 scopus 로고    scopus 로고
    • Identification of an achiral analogue of J-113397 as potent nociceptin/orphanin FQ receptor antagonist
    • Trapella C., Guerrini R., Piccagli L., Calò G., Carrà G., Spagnolo B., et al. Identification of an achiral analogue of J-113397 as potent nociceptin/orphanin FQ receptor antagonist. Bioorg Med Chem 14 (2006) 692-704
    • (2006) Bioorg Med Chem , vol.14 , pp. 692-704
    • Trapella, C.1    Guerrini, R.2    Piccagli, L.3    Calò, G.4    Carrà, G.5    Spagnolo, B.6
  • 41
    • 77952551161 scopus 로고    scopus 로고
    • Dual motor response to l-DOPA and nociceptin/orphanin FQ receptor antagonists in 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP) treated mice: Paradoxical inhibition is relieved by D(2)/D(3) receptor blockade
    • doi:10.1016/j.expneurol.2010.01.014
    • Viaro R, Marti M, Morari M. Dual motor response to l-DOPA and nociceptin/orphanin FQ receptor antagonists in 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP) treated mice: paradoxical inhibition is relieved by D(2)/D(3) receptor blockade. Exp Neurol; doi:10.1016/j.expneurol.2010.01.014.
    • Exp Neurol
    • Viaro, R.1    Marti, M.2    Morari, M.3
  • 42
    • 57049144783 scopus 로고    scopus 로고
    • The nociceptin/orphanin FQ (NOP) receptor antagonist J-113397 enhances the effects of levodopa in the MPTP-lesioned nonhuman primate model of Parkinson's disease
    • Visanji N.P., de Bie R.M., Johnston T.H., McCreary A.C., Brotchie J.M., and Fox S.H. The nociceptin/orphanin FQ (NOP) receptor antagonist J-113397 enhances the effects of levodopa in the MPTP-lesioned nonhuman primate model of Parkinson's disease. Mov Disord 23 (2008) 1922-1925
    • (2008) Mov Disord , vol.23 , pp. 1922-1925
    • Visanji, N.P.1    de Bie, R.M.2    Johnston, T.H.3    McCreary, A.C.4    Brotchie, J.M.5    Fox, S.H.6
  • 43
    • 1642498186 scopus 로고    scopus 로고
    • Modification of nociceptin and morphine tolerance by the selective opiate receptor-like orphan receptor antagonist (-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol (SB-612111)
    • Zaratin P.F., Petrone G., Sbacchi M., Garnier M., Fossati C., Petrillo P., et al. Modification of nociceptin and morphine tolerance by the selective opiate receptor-like orphan receptor antagonist (-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol (SB-612111). J Pharmacol Exp Ther 308 (2004) 454-461
    • (2004) J Pharmacol Exp Ther , vol.308 , pp. 454-461
    • Zaratin, P.F.1    Petrone, G.2    Sbacchi, M.3    Garnier, M.4    Fossati, C.5    Petrillo, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.