-
1
-
-
84987566762
-
Nomenclature and symbolism for amino acids and peptides
-
Abbreviations follow the IUPAC-IUB Joint Commission on Biochemical Nomenclature. Nomenclature and symbolism for amino acids and peptides. Eur. J. Biochem. 1984, 138, 9-37.
-
(1984)
Eur. J. Biochem.
, vol.138
, pp. 9-37
-
-
-
2
-
-
0028971215
-
Orphanin FQ: A neuropeptide that activates an opioidlike G protein-coupled receptor
-
Reinscheid, R. K.; Nothacker, H. P.; Bourson, A.; Ardati, A.; Henningsen, R. A.; Bunzow, J. R.; Grandy, D. K.; Langen, H.; Monsma, F. J., Jr.; Civelli, O. Orphanin FQ: a neuropeptide that activates an opioidlike G protein-coupled receptor. Science 1995, 270, 792-794.
-
(1995)
Science
, vol.270
, pp. 792-794
-
-
Reinscheid, R.K.1
Nothacker, H.P.2
Bourson, A.3
Ardati, A.4
Henningsen, R.A.5
Bunzow, J.R.6
Grandy, D.K.7
Langen, H.8
Monsma Jr., F.J.9
Civelli, O.10
-
3
-
-
0029166509
-
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.; Butour, J. L.; Guillemot, J. C.; Ferrara, P.; Monserrat, B.; Mazarguil, H.; Vassart, G.; Parmentier, M.; Costentin, J. Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor. Nature 1995, 377, 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
Butour, J.L.7
Guillemot, J.C.8
Ferrara, P.9
Monserrat, B.10
Mazarguil, H.11
Vassart, G.12
Parmentier, M.13
Costentin, J.14
-
4
-
-
0001836569
-
Opioid receptors
-
IUPHAR Media Ltd: London
-
Cox, B. M.; Chavkin, C.; Christie, M. J.; Civelli, O.; Evans, C.; Hamon, M. D.; Hoellt, V.; Kieffer, B.; Kitchen, I.; McKnight, A. T.; Meunier, J. C.; Portoghese, P. S. Opioid receptors. The IUPHAR Compendium of Receptor Characterization and Classification, 2nd ed.; IUPHAR Media Ltd: London, 2000; pp 321-333.
-
(2000)
The IUPHAR Compendium of Receptor Characterization and Classification, 2nd Ed.
, pp. 321-333
-
-
Cox, B.M.1
Chavkin, C.2
Christie, M.J.3
Civelli, O.4
Evans, C.5
Hamon, M.D.6
Hoellt, V.7
Kieffer, B.8
Kitchen, I.9
McKnight, A.T.10
Meunier, J.C.11
Portoghese, P.S.12
-
5
-
-
0034850298
-
The molecular and behavioral pharmacology of the orphanin FQ/nociceptin peptide and receptor family
-
Mogil, J. S.; Pasternak, G. W. The molecular and behavioral pharmacology of the orphanin FQ/nociceptin peptide and receptor family. Pharmacol. Rev. 2001, 53, 381-415.
-
(2001)
Pharmacol. Rev.
, vol.53
, pp. 381-415
-
-
Mogil, J.S.1
Pasternak, G.W.2
-
6
-
-
0034101011
-
Pharmacology of nociceptin and its receptor: A novel therapeutic target
-
Calo, G.; Guerrini, R.; Rizzi, A.; Salvadori, S.; Regoli, D. Pharmacology of nociceptin and its receptor: a novel therapeutic target. Br. J. Pharmacol. 2000, 129, 1261-1283.
-
(2000)
Br. J. Pharmacol.
, vol.129
, pp. 1261-1283
-
-
Calo, G.1
Guerrini, R.2
Rizzi, A.3
Salvadori, S.4
Regoli, D.5
-
7
-
-
0037498440
-
Peptide and nonpeptide ligands for the nociceptin/orphanin FQ receptor ORL1: Research tools and potential therapeutic agents
-
Zaveri, N. Peptide and nonpeptide ligands for the nociceptin/orphanin FQ receptor ORL1: Research tools and potential therapeutic agents. Life Sci. 2003, 73, 663-678.
-
(2003)
Life Sci.
, vol.73
, pp. 663-678
-
-
Zaveri, N.1
-
8
-
-
0034712756
-
A synthetic agonist at the orphanin FQ/nociceptin receptor ORL1: Anxiolytic profile in the rat
-
Jenck, F.; Wichmann, J.; Dautzenberg, F. M.; Moreau, J. L.; Ouagazzal, A. M.; Martin, J. R.; Lundstrom, K.; Cesura, A. M.; Poli, S. M.; Roever, S.; Kolczewski, S.; Adam, G.; Kilpatrick, G. A synthetic agonist at the orphanin FQ/nociceptin receptor ORL1: Anxiolytic profile in the rat. Proc. Natl. Acad. Sci. U.S.A. 2000, 97, 4938-4943.
-
(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 4938-4943
-
-
Jenck, F.1
Wichmann, J.2
Dautzenberg, F.M.3
Moreau, J.L.4
Ouagazzal, A.M.5
Martin, J.R.6
Lundstrom, K.7
Cesura, A.M.8
Poli, S.M.9
Roever, S.10
Kolczewski, S.11
Adam, G.12
Kilpatrick, G.13
-
9
-
-
0034683206
-
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.; Miyaji, M.; Azuma, T.; Ichikawa, D.; Nambu, H.; Iguchi, T.; Iwasawa, Y.; Ohta, H. In vitro and in vivo pharmacological characterization of J-113397, a potent and selective non-peptidyl ORL1 receptor antagonist. Eur. J. Pharmacol. 2000, 402, 45-53.
-
(2000)
Eur. J. Pharmacol.
, vol.402
, pp. 45-53
-
-
Ozaki, S.1
Kawamoto, H.2
Itoh, Y.3
Miyaji, M.4
Azuma, T.5
Ichikawa, D.6
Nambu, H.7
Iguchi, T.8
Iwasawa, Y.9
Ohta, H.10
-
10
-
-
0033600840
-
Ligands for kappa-opioid and ORL1 receptors identified from a conformationally constrained peptide combinatorial library
-
Becker, J. A.; Wallace, A.; Garzon, A.; Ingallinella, P.; Bianchi, E.; Cortese, R.; Simonin, F.; Kieffer, B. L.; Pessi, A. Ligands for kappa-opioid and ORL1 receptors identified from a conformationally constrained peptide combinatorial library. J. Biol. Chem. 1999, 274, 27513-27522.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 27513-27522
-
-
Becker, J.A.1
Wallace, A.2
Garzon, A.3
Ingallinella, P.4
Bianchi, E.5
Cortese, R.6
Simonin, F.7
Kieffer, B.L.8
Pessi, A.9
-
11
-
-
0030831767
-
Binding and in vitro activities of peptides with high affinity for the nociceptin/orphanin FQ receptor, ORL1
-
Dooley, C. T.; Spaeth, C. G.; Berzetei-Gurske, I. P.; Craymer, K.; Adapa, I. D.; Brandt, S. R.; Houghten, R. A.; Toll, L. Binding and in vitro activities of peptides with high affinity for the nociceptin/orphanin FQ receptor, ORL1. J. Pharmacol. Exp. Ther. 1997, 283, 735-741.
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 735-741
-
-
Dooley, C.T.1
Spaeth, C.G.2
Berzetei-Gurske, I.P.3
Craymer, K.4
Adapa, I.D.5
Brandt, S.R.6
Houghten, R.A.7
Toll, L.8
-
12
-
-
0030571060
-
The mouse vas deferens: A pharmacological preparation sensitive to nociceptin
-
Calo, G.; Rizzi, A.; Bogoni, G.; Neugebauer, V.; Salvadori, S.; Beani, L.; Regoli, D.; Bianchi, C. The mouse vas deferens: a pharmacological preparation sensitive to nociceptin. Eur. J. Pharmacol. 1998, 311, R3-R5.
-
(1998)
Eur. J. Pharmacol.
, vol.311
-
-
Calo, G.1
Rizzi, A.2
Bogoni, G.3
Neugebauer, V.4
Salvadori, S.5
Beani, L.6
Regoli, D.7
Bianchi, C.8
-
13
-
-
0031006367
-
Address and message sequences for the nociceptin receptor: A structure-activity study of nociceptin-(1-13)-peptide amide
-
Guerrini, R.; Calo, G.; Rizzi, A.; Bianchi, C.; Lazarus, L. H.; Salvadori, S.; Temussi, P. A.; Regoli, D. Address and message sequences for the nociceptin receptor: a structure-activity study of nociceptin-(1-13)-peptide amide. J. Med. Chem. 1897, 40, 1789-1793.
-
(1897)
J. Med. Chem.
, vol.40
, pp. 1789-1793
-
-
Guerrini, R.1
Calo, G.2
Rizzi, A.3
Bianchi, C.4
Lazarus, L.H.5
Salvadori, S.6
Temussi, P.A.7
Regoli, D.8
-
14
-
-
0031974718
-
A new selective antagonist of the nociceptin receptor
-
Guerrini, R.; Calo, G.; Rizzi, A.; Bigoni, R.; Bianchi, C.; Salvadori, S.; Regoli, D. A new selective antagonist of the nociceptin receptor. Br. J. Pharmacol. 1998, 123, 163-165.
-
(1998)
Br. J. Pharmacol.
, vol.123
, pp. 163-165
-
-
Guerrini, R.1
Calo, G.2
Rizzi, A.3
Bigoni, R.4
Bianchi, C.5
Salvadori, S.6
Regoli, D.7
-
15
-
-
0031694279
-
Pharmacological characterization of the nociceptin receptor mediating hyperalgesia in the mouse tail withdrawal assay
-
Calo, G.; Rizzi, A.; Marzola, G.; Guerrini, R.; Salvadori, S.; Beani, L.; Regoli, D.; Bianchi, C. Pharmacological characterization of the nociceptin receptor mediating hyperalgesia in the mouse tail withdrawal assay. Br. J. Pharmacol. 1998, 125, 373-378.
-
(1998)
Br. J. Pharmacol.
, vol.125
, pp. 373-378
-
-
Calo, G.1
Rizzi, A.2
Marzola, G.3
Guerrini, R.4
Salvadori, S.5
Beani, L.6
Regoli, D.7
Bianchi, C.8
-
16
-
-
0032572820
-
2 N-terminal tetrapeptide and discovery of a nociceptin receptor antagonist
-
2 N-terminal tetrapeptide and discovery of a nociceptin receptor antagonist. J. Med. Chem. 1998, 41, 3360-3366.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3360-3366
-
-
Calo, G.1
Guerrini, R.2
Bigoni, R.3
Rizzi, A.4
Bianchi, C.5
Regoli, D.6
Salvadori, S.7
-
17
-
-
0034101842
-
Characterization of [Nphe(1)]nociceptin(1-13)NH(2), a new selective nociceptin receptor antagonist
-
Calo, G.; Guerrini, R.; Bigoni, R.; Rizzi, A.; Marzola, G.; Okawa, H.; Bianchi, C.; Lambert, D. G.; Salvadori, S.; Regoli, D. Characterization of [Nphe(1)]nociceptin(1-13)NH(2), a new selective nociceptin receptor antagonist. Br. J. Pharmacol. 2000, 129, 1183-1193.
-
(2000)
Br. J. Pharmacol.
, vol.129
, pp. 1183-1193
-
-
Calo, G.1
Guerrini, R.2
Bigoni, R.3
Rizzi, A.4
Marzola, G.5
Okawa, H.6
Bianchi, C.7
Lambert, D.G.8
Salvadori, S.9
Regoli, D.10
-
18
-
-
17144435547
-
Further studies on nociceptin-related peptides: Discovery of a new chemical template with antagonist activity on the nociceptin receptor
-
Guerrini, R.; Calo, G.; Bigoni, R.; Rizzi, A.; Varani, K.; Toth, G.; Gessi, S.; Hashiba, E.; Hashimoto, Y.; Lambert, D. G.; Borea, P. A.; Tomatis, R.; Salvadori, S.; Regoli, D. Further studies on nociceptin-related peptides: discovery of a new chemical template with antagonist activity on the nociceptin receptor. J. Med. Chem. 2000, 43, 2805-2813.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2805-2813
-
-
Guerrini, R.1
Calo, G.2
Bigoni, R.3
Rizzi, A.4
Varani, K.5
Toth, G.6
Gessi, S.7
Hashiba, E.8
Hashimoto, Y.9
Lambert, D.G.10
Borea, P.A.11
Tomatis, R.12
Salvadori, S.13
Regoli, D.14
-
19
-
-
0035829420
-
Structure-activity studies of the Phe(4) residue of nociceptin(1-13)- NH(2): Identification of highly potent agonists of the nociceptin/orphanin FQ receptor
-
Guerrini, R.; Calo, G.; Bigoni, R.; Rizzi, D.; Rizzi, A.; Zucchini, M.; Varani, K.; Hashiba, E.; Lambert, D. G.; Toth, G.; Borea, P. A.; Salvadori, S.; Regoli, D. Structure-activity studies of the Phe(4) residue of nociceptin(1-13)-NH(2): identification of highly potent agonists of the nociceptin/orphanin FQ receptor. J. Med. Chem. 2001, 44, 3956-3964.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3956-3964
-
-
Guerrini, R.1
Calo, G.2
Bigoni, R.3
Rizzi, D.4
Rizzi, A.5
Zucchini, M.6
Varani, K.7
Hashiba, E.8
Lambert, D.G.9
Toth, G.10
Borea, P.A.11
Salvadori, S.12
Regoli, D.13
-
20
-
-
0035987104
-
Pharmacological characterisation of [(pX)Phe(4)]-nociceptin(1-13)amide analogues. 1. In vitro studies
-
Bigoni, R.; Rizzi, D.; Rizzi, A.; Camarda, V.; Guerrini, R.; Lambert, D. G.; Hashiba, E.; Berger, H.; Salvadori, S.; Regoli, D.; Calo, G. Pharmacological characterisation of [(pX)Phe(4)]-nociceptin(1-13)amide analogues. 1. In vitro studies. Naunyn-Schmiedeberg's Arch. Pharmacol. 2002, 365, 442-449.
-
(2002)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.365
, pp. 442-449
-
-
Bigoni, R.1
Rizzi, D.2
Rizzi, A.3
Camarda, V.4
Guerrini, R.5
Lambert, D.G.6
Hashiba, E.7
Berger, H.8
Salvadori, S.9
Regoli, D.10
Calo, G.11
-
21
-
-
0035987107
-
Pharmacological characterisation of [(pX)Phe(4)]-nociceptin(1-13)amide analogues. 2. In vivo studies
-
Rizzi, A.; Salis, B.; Ciccocioppo, R.; Marzola, G.; Bigoni, R.; Guerrini, R.; Massi, M.; Madeddu, P.; Salvadori, S.; Regoli, D.; Calo, G. Pharmacological characterisation of [(pX)Phe(4)]-nociceptin(1-13)amide analogues. 2. In vivo studies. Naunyn-Schmiedeberg's Arch. Pharmacol. 2002, 365, 450-456.
-
(2002)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.365
, pp. 450-456
-
-
Rizzi, A.1
Salis, B.2
Ciccocioppo, R.3
Marzola, G.4
Bigoni, R.5
Guerrini, R.6
Massi, M.7
Madeddu, P.8
Salvadori, S.9
Regoli, D.10
Calo, G.11
-
22
-
-
0034687553
-
Highly potent nociceptin analog containing the Arg-Lys triple repeat
-
Okada, K.; Sujaku, T.; Chuman, Y.; Nakashima, R.; Nose, T.; Costa, T.; Yamada, Y.; Yokoyama, M.; Nagahisa, A.; Shimohigashi, Y. Highly potent nociceptin analog containing the Arg-Lys triple repeat. Biochem. Biophys. Res. Commun. 2000, 278, 493-498.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.278
, pp. 493-498
-
-
Okada, K.1
Sujaku, T.2
Chuman, Y.3
Nakashima, R.4
Nose, T.5
Costa, T.6
Yamada, Y.7
Yokoyama, M.8
Nagahisa, A.9
Shimohigashi, Y.10
-
23
-
-
0033042973
-
Characterization of nociceptin receptors in the periphery: In vitro and in vivo studies
-
Bigoni, R.; Giuliani, S.; Calo, G.; Rizzi, A.; Guerrini, R.; Salvadori, S.; Regoli, D.; Maggi, C. A. Characterization of nociceptin receptors in the periphery: in vitro and in vivo studies. Naunyn-Schmiedeberg's Arch. Pharmacol. 1999, 359, 160-167.
-
(1999)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.359
, pp. 160-167
-
-
Bigoni, R.1
Giuliani, S.2
Calo, G.3
Rizzi, A.4
Guerrini, R.5
Salvadori, S.6
Regoli, D.7
Maggi, C.A.8
-
24
-
-
0032436171
-
Molecular modelling of the ORL1 receptor and its complex with nociceptin
-
Topham, C. M.; Mouledous, L.; Poda, G.; Maigret, B.; Meunier, J. C. Molecular modelling of the ORL1 receptor and its complex with nociceptin. Protein Eng. 1898, 11, 1163-1179.
-
(1898)
Protein Eng.
, vol.11
, pp. 1163-1179
-
-
Topham, C.M.1
Mouledous, L.2
Poda, G.3
Maigret, B.4
Meunier, J.C.5
-
25
-
-
14344252989
-
2 (UFP-102), a highly potent and selective agonist of the nociceptin/orphanin FQ receptor
-
in press
-
2 (UFP-102), a highly potent and selective agonist of the nociceptin/orphanin FQ receptor. J. Pharmacol. Exp. Ther., in press.
-
J. Pharmacol. Exp. Ther.
-
-
Carra, G.1
Rizzi, A.2
Guerrini, R.3
Barnes, T.A.4
McDonald, J.5
Hebbes, C.P.6
Mela, F.7
Kenigs, V.A.8
Marzola, G.9
Rizzi, D.10
Gavioli, E.11
Zucchini, S.12
Regoli, D.13
Morari, M.14
Salvadori, S.15
Rowbotham, D.J.16
Lambert, D.G.17
Kapusta, D.R.18
Calo, G.19
-
26
-
-
0032588075
-
2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptors
-
2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptors. Br. J. Pharmacol. 1999, 127, 123-130.
-
(1999)
Br. J. Pharmacol.
, vol.127
, pp. 123-130
-
-
Okawa, H.1
Nicol, B.2
Bigoni, R.3
Hirst, R.A.4
Calo, G.5
Guerrini, R.6
Rowbotham, D.J.7
Smart, D.8
McKnight, A.T.9
Lambert, D.G.10
-
28
-
-
0141841768
-
Partial agonist behaviour depends upon the level of nociceptin/orphanin FQ receptor expression: Studies using the ecdysone-inducible mammalian expression system
-
McDonald, J.; Barnes, T. A.; Okawa, H.; Williams, J.; Calo, G.; Rowbotham, D. J.; Lambert, D. G. Partial agonist behaviour depends upon the level of nociceptin/orphanin FQ receptor expression: studies using the ecdysone-inducible mammalian expression system. Br. J. Pharmacol. 2003, 140, 61-70.
-
(2003)
Br. J. Pharmacol.
, vol.140
, pp. 61-70
-
-
McDonald, J.1
Barnes, T.A.2
Okawa, H.3
Williams, J.4
Calo, G.5
Rowbotham, D.J.6
Lambert, D.G.7
-
29
-
-
0036015187
-
2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptor
-
2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptor. Br. J. Pharmacol. 2002, 136, 303-311.
-
(2002)
Br. J. Pharmacol.
, vol.136
, pp. 303-311
-
-
Calo, G.1
Rizzi, A.2
Rizzi, D.3
Bigoni, R.4
Guerrini, R.5
Marzola, G.6
Marti, M.7
McDonald, J.8
Morari, M.9
Lambert, D.G.10
Salvadori, S.11
Regoli, D.12
-
30
-
-
12144288104
-
Pharmacological profile of nociceptin/orphanin FQ receptors regulating 5-hydroxytryptamine release in the mouse neocortex
-
Mela, F.; Marti, M.; Ulazzi, L.; Vaccari, E.; Zucchini, S.; Trapella, C.; Salvadori, S.; Beani, L.; Bianchi, C.; Morari, M. Pharmacological profile of nociceptin/orphanin FQ receptors regulating 5-hydroxytryptamine release in the mouse neocortex. Eur. J. Neurosci. 2004, 19, 1317-1324.
-
(2004)
Eur. J. Neurosci.
, vol.19
, pp. 1317-1324
-
-
Mela, F.1
Marti, M.2
Ulazzi, L.3
Vaccari, E.4
Zucchini, S.5
Trapella, C.6
Salvadori, S.7
Beani, L.8
Bianchi, C.9
Morari, M.10
-
31
-
-
14944366716
-
UFP-101 is a competitive antagonist of N/OFQ receptors mediating inwardly rectifying K+ channel activation in rat periaquedutal gray slices
-
Portugal, July 10-14
-
Chiou, L. C.; Liao, Y. Y.; Calo', G.; Guerrini, R. UFP-101 is a competitive antagonist of N/OFQ receptors mediating inwardly rectifying K+ channel activation in rat periaquedutal gray slices. Presented at the Meeting of the Federation of European Neurosciences Lisbon, Portugal, July 10-14, 2004.
-
(2004)
Meeting of the Federation of European Neurosciences Lisbon
-
-
Chiou, L.C.1
Liao, Y.Y.2
Calo, G.3
Guerrini, R.4
-
32
-
-
14944368433
-
Effects of NOP ligands in the electrically stimulated human bronchus
-
Camerino, Italy, September 15
-
Basso, M.; Naline, E.; Calo, G.; Guerrini, R.; Regoli, D.; Advenier, C. Effects of NOP ligands in the electrically stimulated human bronchus. Presented at the Meeting of La Nocicettina/Orfanina FQ Ed Il Suo Recettore, Camerino, Italy, September 15, 2003.
-
(2003)
Meeting of la Nocicettina/Orfanina FQ Ed Il Suo Recettore
-
-
Basso, M.1
Naline, E.2
Calo, G.3
Guerrini, R.4
Regoli, D.5
Advenier, C.6
-
33
-
-
14944346191
-
Chemotactic effects of nociceptin/orphanin FQ on human monocytes are mediated by NOP receptor activation
-
Camerino, Italy, September 15
-
Trombella, S.; Vergura, R.; Guerrini, R.; Calo, G.; Spisani, S. Chemotactic effects of nociceptin/orphanin FQ on human monocytes are mediated by NOP receptor activation. Presented at the Meeting of La Nocicettina/Orfanina FQ Ed Il Suo Recettore, Camerino, Italy, September 15, 2003.
-
(2003)
Meeting of la Nocicettina/Orfanina FQ Ed Il Suo Recettore
-
-
Trombella, S.1
Vergura, R.2
Guerrini, R.3
Calo, G.4
Spisani, S.5
-
34
-
-
20144379060
-
Antinociceptive effects induced by spinal nociceptin/orphanin FQ administration are due to NOP receptor activation: Phamacological and genetic evidences in mice
-
Porto, Portugal
-
Rizzi, A.; Marzola, G.; Gavioli, E. C.; Guerrini, R.; Zucchini, S.; Kenigs, V. A.; Kapusta, D. R.; Salvadori, S.; Regoli, D.; Calo, G. Antinociceptive effects induced by spinal nociceptin/orphanin FQ administration are due to NOP receptor activation: phamacological and genetic evidences in mice. Presented at EPHAR, the Federation of European Pharmacological Societies, Porto, Portugal, 2004.
-
(2004)
EPHAR, the Federation of European Pharmacological Societies
-
-
Rizzi, A.1
Marzola, G.2
Gavioli, E.C.3
Guerrini, R.4
Zucchini, S.5
Kenigs, V.A.6
Kapusta, D.R.7
Salvadori, S.8
Regoli, D.9
Calo, G.10
-
35
-
-
0036201874
-
Nociceptin receptor antagonists display antidepressant-like properties in the mouse forced swimming test
-
Redrobe, J. P.; Calo, G.; Regoli, D.; Quirion, R. Nociceptin receptor antagonists display antidepressant-like properties in the mouse forced swimming test. Naunyn-Sehmiedeberg's Arch. Pharmacol. 2002, 365, 164-167.
-
(2002)
Naunyn-Sehmiedeberg's Arch. Pharmacol.
, vol.365
, pp. 164-167
-
-
Redrobe, J.P.1
Calo, G.2
Regoli, D.3
Quirion, R.4
-
36
-
-
0038730667
-
Blockade of nociceptin/orphanin FQ-NOP receptor signalling produces antidepressant-like effects: Pharmacological and genetic evidences from the mouse forced swimming test
-
Gavioli, E. C.; Marzola, G.; Guerrini, R.; Bertorelli, R.; Zucchini, S.; De Lima, T. C.; Rae, G. A.; Salvadori, S.; Regoli, D.; Calo, G. Blockade of nociceptin/orphanin FQ-NOP receptor signalling produces antidepressant-like effects: pharmacological and genetic evidences from the mouse forced swimming test. Eur. J. Neurosci. 2003, 17, 1987-1990.
-
(2003)
Eur. J. Neurosci.
, vol.17
, pp. 1987-1990
-
-
Gavioli, E.C.1
Marzola, G.2
Guerrini, R.3
Bertorelli, R.4
Zucchini, S.5
De Lima, T.C.6
Rae, G.A.7
Salvadori, S.8
Regoli, D.9
Calo, G.10
-
37
-
-
3042550222
-
Antidepressant-like effects of the nociceptin/orphanin FQ receptor antagonist UFP-101: New evidences in rats and mice
-
Gavioli, E. C.; Vaughan, C. W.; Marzola, G.; Guerrini, R.; Mitchell, V. A.; Zucchini, S.; De Lima, T. C.; Rae, G. A.; Salvadori, S.; Regoli, D.; Calo, G. Antidepressant-like effects of the nociceptin/orphanin FQ receptor antagonist UFP-101: new evidences in rats and mice. Naunyn-Schmiedeberg's Arch. Pharmacol. 2004, 369, 547-553.
-
(2004)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.369
, pp. 547-553
-
-
Gavioli, E.C.1
Vaughan, C.W.2
Marzola, G.3
Guerrini, R.4
Mitchell, V.A.5
Zucchini, S.6
De Lima, T.C.7
Rae, G.A.8
Salvadori, S.9
Regoli, D.10
Calo, G.11
-
38
-
-
0037732805
-
Effects of nociceptin/orphanin FQ receptor ligands on blood pressure, heart rate and plasma catecholamine concentrations in guinea pigs
-
Hashiba, E.; Hirota, K.; Kudo, T.; Calo', G.; Guerrini, R.; Matsuki, A. Effects of nociceptin/orphanin FQ receptor ligands on blood pressure, heart rate and plasma catecholamine concentrations in guinea pigs. Naunyn-Schmiedeberg's Arch. Pharmacol. 2003, 367, 342-347.
-
(2003)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.367
, pp. 342-347
-
-
Hashiba, E.1
Hirota, K.2
Kudo, T.3
Calo, G.4
Guerrini, R.5
Matsuki, A.6
-
39
-
-
71849104860
-
Protein measurements with the Folin phenol reagent
-
Lowry, O. H.; Nira, J.; Rosenbrough, A.; Farr, L.; Randall, R. J. Protein measurements with the Folin phenol reagent. J. Biol. Chem. 1951, 193, 265-275.
-
(1951)
J. Biol. Chem.
, vol.193
, pp. 265-275
-
-
Lowry, O.H.1
Nira, J.2
Rosenbrough, A.3
Farr, L.4
Randall, R.J.5
-
40
-
-
0345490945
-
International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology
-
Neubig, R. R.; Spedding, M.; Kenakin, T.; Christopoulos, A. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology. Pharmacol. Rev. 2003, 55, 597-606.
-
(2003)
Pharmacol. Rev.
, vol.55
, pp. 597-606
-
-
Neubig, R.R.1
Spedding, M.2
Kenakin, T.3
Christopoulos, A.4
-
41
-
-
0035151569
-
Characterisation and comparison of novel ligands for the nociceptin/orphanin FQ receptor
-
Hashiba, E.; Harrison, C.; Galo, G.; Guerrini, R.; Rowbotham, D. J.; Smith, G.; Lambert, D. G. Characterisation and comparison of novel ligands for the nociceptin/orphanin FQ receptor. Naunyn-Schmiedeberg's Arch. Pharmacol. 2001, 363, 28-33.
-
(2001)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.363
, pp. 28-33
-
-
Hashiba, E.1
Harrison, C.2
Galo, G.3
Guerrini, R.4
Rowbotham, D.J.5
Smith, G.6
Lambert, D.G.7
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