-
1
-
-
0023200698
-
Nociceptive action of excitatory amino acids in the mouse: Effects of spinally administered opioids, phencyclidine and sigma agonists
-
Aanonsen, L.M. and Wilcox, G., Nociceptive action of excitatory amino acids in the mouse: effects of spinally administered opioids, phencyclidine and sigma agonists, J. Pharmacol. Exp. Ther., 243 (1987) 9-19.
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.243
, pp. 9-19
-
-
Aanonsen, L.M.1
Wilcox, G.2
-
2
-
-
0021215525
-
The behavioural effects of an N-methylaspartate receptor antagonist following application to the lumbar spinal cord of conscious rats
-
Cahusac, P.M.B., Evans, R.H., Hill, R.G., Rodriquez, R.E. and Smith, D.A.S., The behavioural effects of an N-methylaspartate receptor antagonist following application to the lumbar spinal cord of conscious rats, Neuropharmacology, 23 (1984) 719-724.
-
(1984)
Neuropharmacology
, vol.23
, pp. 719-724
-
-
Cahusac, P.M.B.1
Evans, R.H.2
Hill, R.G.3
Rodriquez, R.E.4
Smith, D.A.S.5
-
3
-
-
0026640290
-
The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury
-
Coderre, T.J. and Melzack, R., The contribution of excitatory amino acids to central sensitization and persistent nociception after formalin-induced tissue injury, J. Neurosci., 12 (1992) 3665-3670.
-
(1992)
J. Neurosci.
, vol.12
, pp. 3665-3670
-
-
Coderre, T.J.1
Melzack, R.2
-
4
-
-
0028594101
-
The utility of excitatory amino acid (EAA) antagonists as analgesic agents. I. Comparison of the antinociceptive activity of various classes of EAA antagonists in mechanical, thermal and chemical nociceptive tests
-
Coderre, T.J. and Van Empel, I., The utility of excitatory amino acid (EAA) antagonists as analgesic agents. I. Comparison of the antinociceptive activity of various classes of EAA antagonists in mechanical, thermal and chemical nociceptive tests, Pain, 59 (1992) 345-352.
-
(1992)
Pain
, vol.59
, pp. 345-352
-
-
Coderre, T.J.1
Van Empel, I.2
-
5
-
-
0026096452
-
The local monoaminergic dependency of spinal ketamine
-
Crisp, T., Perotti, J.M., Smith, D.L., Stafinsky, J.L. and Smith, D.J., The local monoaminergic dependency of spinal ketamine, Eur. J. Pharmacol., 194 (1991) 167-172.
-
(1991)
Eur. J. Pharmacol.
, vol.194
, pp. 167-172
-
-
Crisp, T.1
Perotti, J.M.2
Smith, D.L.3
Stafinsky, J.L.4
Smith, D.J.5
-
6
-
-
0002261078
-
A method for determining loss of pain sensation
-
D'Amour, F.E. and Smith, D.L., A method for determining loss of pain sensation, J. Pharmacol. Exp. Ther., 72 (1941) 74-79.
-
(1941)
J. Pharmacol. Exp. Ther.
, vol.72
, pp. 74-79
-
-
D'Amour, F.E.1
Smith, D.L.2
-
7
-
-
0025788197
-
Hyperalgesia and myoclonus with intrathecal infusion of high-dose morphine
-
De Conno, F., Caraceni, A., Martini, C., Spoldi, E., Salvetti, M. and Ventafridda, V., Hyperalgesia and myoclonus with intrathecal infusion of high-dose morphine, Pain, 47 (1991) 337-339.
-
(1991)
Pain
, vol.47
, pp. 337-339
-
-
De Conno, F.1
Caraceni, A.2
Martini, C.3
Spoldi, E.4
Salvetti, M.5
Ventafridda, V.6
-
8
-
-
0024800274
-
Morphine (intracerebroventricular) activates spinal systems to inhibit behavior induced by putative pain neurotransmitters
-
Delander, G.E. and Wahl, J.J., Morphine (intracerebroventricular) activates spinal systems to inhibit behavior induced by putative pain neurotransmitters, J. Pharmacol. Exp. Ther., 251 (1989) 1090-1095.
-
(1989)
J. Pharmacol. Exp. Ther.
, vol.251
, pp. 1090-1095
-
-
Delander, G.E.1
Wahl, J.J.2
-
9
-
-
0026008423
-
Antagonism at the glycine on the NMDA receptor reduces spinal nociception in the rat
-
Dickenson, A.H. and Ayder, E., Antagonism at the glycine on the NMDA receptor reduces spinal nociception in the rat, Neurosci. Lett., 121 (1991) 263-266.
-
(1991)
Neurosci. Lett.
, vol.121
, pp. 263-266
-
-
Dickenson, A.H.1
Ayder, E.2
-
10
-
-
0025021299
-
Differential effects of excitatory amino acid antagonists on dorsal horn nociceptive neurones in the rat
-
Dickenson, A.H. and Sullivan, A.F., Differential effects of excitatory amino acid antagonists on dorsal horn nociceptive neurones in the rat, Brain Res., 506 (1990) 31-39.
-
(1990)
Brain Res.
, vol.506
, pp. 31-39
-
-
Dickenson, A.H.1
Sullivan, A.F.2
-
11
-
-
0027404879
-
GYKI 52466, a 2,3-benzodiazepine, is a highly selective, non-competitive antagonist of AMPA/kainate receptor responses
-
Donevan, S.D. and Rogawski, M.A., GYKI 52466, a 2,3-benzodiazepine, is a highly selective, non-competitive antagonist of AMPA/kainate receptor responses, Neuron, 10 (1993) 51-59.
-
(1993)
Neuron
, vol.10
, pp. 51-59
-
-
Donevan, S.D.1
Rogawski, M.A.2
-
12
-
-
0028281628
-
Antinociception induced by 3-(±)-2-carboxypiperazine-4-yl-propyl-1-phosphonic acid (CPP), an N-methyl-D-aspartate (NMDA) competitive antagonist, plus 6,7-dinitroquinoxaline-2,3-dione (DNQX), a non-NMDa antagonist, differs from that induced by MK-801 plus DNQX
-
Goettl, V.M. and Larson, A.A., Antinociception induced by 3-((±)-2-carboxypiperazine-4-yl-propyl-1-phosphonic acid (CPP), an N-methyl-D-aspartate (NMDA) competitive antagonist, plus 6,7-dinitroquinoxaline-2,3-dione (DNQX), a non-NMDA antagonist, differs from that induced by MK-801 plus DNQX, Brain Res., 642 (1994) 334-338.
-
(1994)
Brain Res.
, vol.642
, pp. 334-338
-
-
Goettl, V.M.1
Larson, A.A.2
-
13
-
-
0001249750
-
Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: Selective binding to open channels
-
Huettner, J.E. and Bean, B.P., Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: selective binding to open channels, Proc. Natl. Acad. Sci. USA, 85 (1988) 1307-1311.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 1307-1311
-
-
Huettner, J.E.1
Bean, B.P.2
-
14
-
-
0018956018
-
Intrathecal morphine in mice: A new technique
-
Hylden, J.L.K. and Wilcox, G.L., Intrathecal morphine in mice: a new technique, Eur. J. Pharmacol., 67 (1980) 313-316.
-
(1980)
Eur. J. Pharmacol.
, vol.67
, pp. 313-316
-
-
Hylden, J.L.K.1
Wilcox, G.L.2
-
15
-
-
0028862819
-
Synthesis and structure-activity relationships of substituted 1,4-dihydroquinoxaline-2,3-diones: Antagonists of W-methyl-D-aspartate (NMDA) receptor glycine sites and non-NMDA glutamate receptors
-
Keana, J.F.W., Kher, S.M., Cai, S.X., Dinsmore, C.M., Glenn, A.G., Guastella, J., Huang, J.-C., Ilyin, V., Lü, Y., Mouser, P.L., Woodward, R.M. and Weber, E., Synthesis and structure-activity relationships of substituted 1,4-dihydroquinoxaline-2,3-diones: antagonists of W-methyl-D-aspartate (NMDA) receptor glycine sites and non-NMDA glutamate receptors, J. Med. Chem., 38 (1995) 4367-4379.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4367-4379
-
-
Keana, J.F.W.1
Kher, S.M.2
Cai, S.X.3
Dinsmore, C.M.4
Glenn, A.G.5
Guastella, J.6
Huang, J.-C.7
Ilyin, V.8
Lü, Y.9
Mouser, P.L.10
Woodward, R.M.11
Weber, E.12
-
16
-
-
0028057920
-
The NMDA antagonist 3-(2-carboxypiperazine-4-yl)propyl-1-phosphonic acid (CPP) has antinociceptive effect after intrathecal injection in the rat
-
Kristensen, J.D., Karlsten, R., Gordh, T. and Berge, O.-G., The NMDA antagonist 3-(2-carboxypiperazine-4-yl)propyl-1-phosphonic acid (CPP) has antinociceptive effect after intrathecal injection in the rat, Pain, 56 (1994) 59-67.
-
(1994)
Pain
, vol.56
, pp. 59-67
-
-
Kristensen, J.D.1
Karlsten, R.2
Gordh, T.3
Berge, O.-G.4
-
17
-
-
0028240929
-
3′-(Arylmethyl)- and 3′-(aryloxy)-3-phenyl-4-hydroxyquinolin-2(1H)-ones: Orally active antagonists of the glycine site on the NMDA receptor
-
Kulagowski, J.J., Baker, R., Curtis, N.R., Leeson, P.D., Mawer, I.M., Moseley, A.M., Ridgill, M.P., Rowley, M., Stansfield, I., Foster, A.C., Grimwood, S., Hill, R.G., Kemp, J.A., Marshall, G.R., Saywell, K.L. and Tricklebank, M.D., 3′-(Arylmethyl)- and 3′-(aryloxy)-3-phenyl-4-hydroxyquinolin-2(1H)-ones: orally active antagonists of the glycine site on the NMDA receptor, J. Med. Chem., 37 (1994) 1402-1405.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1402-1405
-
-
Kulagowski, J.J.1
Baker, R.2
Curtis, N.R.3
Leeson, P.D.4
Mawer, I.M.5
Moseley, A.M.6
Ridgill, M.P.7
Rowley, M.8
Stansfield, I.9
Foster, A.C.10
Grimwood, S.11
Hill, R.G.12
Kemp, J.A.13
Marshall, G.R.14
Saywell, K.L.15
Tricklebank, M.D.16
-
18
-
-
0027522536
-
Further concerns over Cheng-Prusoff analysis
-
Leff, P. and Dougall, I.G., Further concerns over Cheng-Prusoff analysis, Trends Pharmacol. Sci., 14 (1993) 110-112.
-
(1993)
Trends Pharmacol. Sci.
, vol.14
, pp. 110-112
-
-
Leff, P.1
Dougall, I.G.2
-
19
-
-
0023152733
-
CPP, a selective N-methyl-D-aspartate (NMDA)-type receptor antagonist: Characterization in vitro and in vivo
-
Lehmann, J., Schneider, J., McPherson, S., Murphy, D.E., Bernard, P., Tsai, C., Bennett, D.A., Pastor, G., Steel, D.J., Boehm, C., Cheney, D.L., Liebman, J.M., William, M. and Wood, P.L., CPP, a selective N-methyl-D-aspartate (NMDA)-type receptor antagonist: characterization in vitro and in vivo, J. Pharmacol. Exp. Ther., 240 (1987) 737-746.
-
(1987)
J. Pharmacol. Exp. Ther.
, vol.240
, pp. 737-746
-
-
Lehmann, J.1
Schneider, J.2
McPherson, S.3
Murphy, D.E.4
Bernard, P.5
Tsai, C.6
Bennett, D.A.7
Pastor, G.8
Steel, D.J.9
Boehm, C.10
Cheney, D.L.11
Liebman, J.M.12
William, M.13
Wood, P.L.14
-
20
-
-
0026537712
-
The non-NMDA antagonists, NBQX and GYKI 52466, protect against cortical and striatal cell loss following transient global ischaemia in the rat
-
Le Peillet, E., Babak, A., Moncada, C. and Meldrum, B.S., The non-NMDA antagonists, NBQX and GYKI 52466, protect against cortical and striatal cell loss following transient global ischaemia in the rat, Brain Res., 571 (1992) 115-120.
-
(1992)
Brain Res.
, vol.571
, pp. 115-120
-
-
Le Peillet, E.1
Babak, A.2
Moncada, C.3
Meldrum, B.S.4
-
21
-
-
84951384024
-
A simplified method of dose-effects experiments
-
Litchfield, J.T. and Wilcoxon, F., A simplified method of dose-effects experiments, J. Pharmacol. Exp. Ther., 96 (1949) 99-113.
-
(1949)
J. Pharmacol. Exp. Ther.
, vol.96
, pp. 99-113
-
-
Litchfield, J.T.1
Wilcoxon, F.2
-
22
-
-
0030300178
-
Attenuation of nociceptive responses by ACEA-1021, a competitive NMDa receptor/glycine site antagonist, in the mice
-
in press
-
Lutfy, K. and Weber, E., Attenuation of nociceptive responses by ACEA-1021, a competitive NMDA receptor/glycine site antagonist, in the mice, Brain Res., in press.
-
Brain Res.
-
-
Lutfy, K.1
Weber, E.2
-
23
-
-
0028097637
-
Inhibition of clonic seizure-like excitatory effects induced by intrathecal morphine using two NMDA receptor antagonists: MK-801 and ACEA-1011
-
Lutfy, K., Woodward, R.M., Keana, J.F.W. and Weber, E., Inhibition of clonic seizure-like excitatory effects induced by intrathecal morphine using two NMDA receptor antagonists: MK-801 and ACEA-1011, Eur. J. Pharmacol., 252 (1994) 261-266.
-
(1994)
Eur. J. Pharmacol.
, vol.252
, pp. 261-266
-
-
Lutfy, K.1
Woodward, R.M.2
Keana, J.F.W.3
Weber, E.4
-
24
-
-
0030603088
-
Inhibition of morphine tolerance by NMDA receptor antagonists in the formalin test
-
Lutfy, K., Shen, K.-Z., Woodward, R.M. and Weber, E., Inhibition of morphine tolerance by NMDA receptor antagonists in the formalin test, Brain Res., 731 (1996) 171-181.
-
(1996)
Brain Res.
, vol.731
, pp. 171-181
-
-
Lutfy, K.1
Shen, K.-Z.2
Woodward, R.M.3
Weber, E.4
-
25
-
-
0025970493
-
Actions of ketamine, phencyclidine and MK-801 on NMDA receptor currents in cultured mouse hippocampal neurones
-
Lond.
-
MacDonald, J.F., Bartlett, M.C., Mody, I., Paphapill, P., Reynolds, J.N., Slater, M.W., Schneiderman, J.H. and Pennefather, P.S., Actions of ketamine, phencyclidine and MK-801 on NMDA receptor currents in cultured mouse hippocampal neurones, J. Physiol. (Lond.), 432 (1991) 483-508.
-
(1991)
J. Physiol.
, vol.432
, pp. 483-508
-
-
MacDonald, J.F.1
Bartlett, M.C.2
Mody, I.3
Paphapill, P.4
Reynolds, J.N.5
Slater, M.W.6
Schneiderman, J.H.7
Pennefather, P.S.8
-
26
-
-
0025980364
-
Neurokinin and NMDa antagonists (but not a kainic acid antagonist) are antinociceptive in the mouse formalin model
-
Murray, C.W., Cowan, A. and Larson, A.A., Neurokinin and NMDA antagonists (but not a kainic acid antagonist) are antinociceptive in the mouse formalin model, Pain, 44 (1991) 179-185.
-
(1991)
Pain
, vol.44
, pp. 179-185
-
-
Murray, C.W.1
Cowan, A.2
Larson, A.A.3
-
27
-
-
0026504523
-
Antinociceptive actions of different classes of excitatory amino acids receptor antagonists in mice
-
Näsström, J., Karlsson, U. and Post, C., Antinociceptive actions of different classes of excitatory amino acids receptor antagonists in mice, Eur. J. Pharmacol., 212 (1992) 21-29.
-
(1992)
Eur. J. Pharmacol.
, vol.212
, pp. 21-29
-
-
Näsström, J.1
Karlsson, U.2
Post, C.3
-
28
-
-
0027274702
-
Systemic or intracerebroventricular injection of NMDA receptor antagonists attenuates the antinociceptive activity of intrathecally administered NMDA receptor antagonists
-
Näsström, J., Karlsson, U. and Berge, O.-G., Systemic or intracerebroventricular injection of NMDA receptor antagonists attenuates the antinociceptive activity of intrathecally administered NMDA receptor antagonists, Brain Res., 623 (1993) 47-55.
-
(1993)
Brain Res.
, vol.623
, pp. 47-55
-
-
Näsström, J.1
Karlsson, U.2
Berge, O.-G.3
-
29
-
-
0020046970
-
The involvement of opiate and monoaminergic neuronal systems in the analgesic effects of ketamine
-
Pekoe, G.M. and Smith, D.J., The involvement of opiate and monoaminergic neuronal systems in the analgesic effects of ketamine, Pain, 12 (1982) 57-73.
-
(1982)
Pain
, vol.12
, pp. 57-73
-
-
Pekoe, G.M.1
Smith, D.J.2
-
30
-
-
0025297594
-
Spinal antinociceptive effects of excitatory amino acid antagonists: Quisqualate modulates the action of N-methyl-D-aspartate
-
Raigorodsky, G. and Urca, G., Spinal antinociceptive effects of excitatory amino acid antagonists: quisqualate modulates the action of N-methyl-D-aspartate, Eur. J. Pharmacol., 182 (1990) 37-47.
-
(1990)
Eur. J. Pharmacol.
, vol.182
, pp. 37-47
-
-
Raigorodsky, G.1
Urca, G.2
-
31
-
-
0026669928
-
The intrathecal administration of excitatory amino acid receptor antagonists selectively attenuated carrageenan-induced behavioral hyperalgesia in rats
-
Ren, K., Williams, G.M., Hylden, J.L.K., Ruda, M.A. and Dubner, R., The intrathecal administration of excitatory amino acid receptor antagonists selectively attenuated carrageenan-induced behavioral hyperalgesia in rats, Eur. J. Pharmacol., 219 (1992) 235-243.
-
(1992)
Eur. J. Pharmacol.
, vol.219
, pp. 235-243
-
-
Ren, K.1
Williams, G.M.2
Hylden, J.L.K.3
Ruda, M.A.4
Dubner, R.5
-
32
-
-
0025117827
-
2,3-Dihydro-6-nitro-7-sulfamoyl-benzo(F)quinoxaline: A neuroprotectant for cerebral ischemia
-
Washington DC
-
Sheardown, M.J., Neilsen, E.O., Hansen, A.J., Jacobsen, P. and Honore, T., 2,3-Dihydro-6-nitro-7-sulfamoyl-benzo(F)quinoxaline: a neuroprotectant for cerebral ischemia, Science (Washington DC), 247 (1990) 571-574.
-
(1990)
Science
, vol.247
, pp. 571-574
-
-
Sheardown, M.J.1
Neilsen, E.O.2
Hansen, A.J.3
Jacobsen, P.4
Honore, T.5
-
33
-
-
0025186838
-
Enantiomers of HA-966 (3-amino-1-hydroxypyrrolid-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/W-methyl-D-aspartate receptor antagonist, but ( - )-HA-966 is a potent γ-butyrolactone-like sedative
-
Singh, L., Donald, A.E., Foster, A.C., Hutson, P.H., Iverson, L.L., Iverson, S.D., Kemp, J.A., Lesson, P.D., Marshall, G.R., Oies, R.J., Priestley, T., Thorn, L., Tricklebank, M.D., Vass, C.A. and Williams, B.J., Enantiomers of HA-966 (3-amino-1-hydroxypyrrolid-2-one) exhibit distinct central nervous system effects: (+)-HA-966 is a selective glycine/W-methyl-D-aspartate receptor antagonist, but ( - )-HA-966 is a potent γ-butyrolactone-like sedative, Proc. Natl. Acad. Sci. USA, 87 (1990) 347-351.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 347-351
-
-
Singh, L.1
Donald, A.E.2
Foster, A.C.3
Hutson, P.H.4
Iverson, L.L.5
Iverson, S.D.6
Kemp, J.A.7
Lesson, P.D.8
Marshall, G.R.9
Oies, R.J.10
Priestley, T.11
Thorn, L.12
Tricklebank, M.D.13
Vass, C.A.14
Williams, B.J.15
-
34
-
-
0025884961
-
The non-N-methyl-D-aspartate receptor antagonists, GYKI 52466 and NBQX are anticonvulsant in two animal models of reflex epilepsy
-
Smith, S.E., Dürmüller, N. and Meldrum, B.S., The non-N-methyl-D-aspartate receptor antagonists, GYKI 52466 and NBQX are anticonvulsant in two animal models of reflex epilepsy, Eur. J. Pharmacol., 201 (1991) 179-183.
-
(1991)
Eur. J. Pharmacol.
, vol.201
, pp. 179-183
-
-
Smith, S.E.1
Dürmüller, N.2
Meldrum, B.S.3
-
35
-
-
0000359998
-
Paradoxical pain following high-dose spinal morphine
-
Stillman, M.J., Moulin, D.E. and Foley, K.E., Paradoxical pain following high-dose spinal morphine, Pain, 4 (Suppl.) (1987) S389.
-
(1987)
Pain
, vol.4
, Issue.SUPPL.
-
-
Stillman, M.J.1
Moulin, D.E.2
Foley, K.E.3
-
36
-
-
0003508424
-
-
Springer-Verlag, New York
-
Tallarida, R.J. and Murray, R.B., Manual of Pharmacologic Calculations with Computer Programs, 2nd Edn. Springer-Verlag, New York, 1987, pp. 159-164.
-
(1987)
Manual of Pharmacologic Calculations with Computer Programs, 2nd Edn.
, pp. 159-164
-
-
Tallarida, R.J.1
Murray, R.B.2
-
37
-
-
0001790659
-
Excitatory neurotransmitters and pain
-
M.R. Bond, J.E. Charlton and C.J. Woolf (Eds.), IASP, Seattle
-
Wilcox, G.L., Excitatory neurotransmitters and pain. In: M.R. Bond, J.E. Charlton and C.J. Woolf (Eds.), Proc. VIth World Congress on Pain, IASP, Seattle, 1991, pp. 97-117.
-
(1991)
Proc. VIth World Congress on Pain
, pp. 97-117
-
-
Wilcox, G.L.1
-
38
-
-
0028988215
-
Differential antagonism of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-preferring and kainatepreferring receptors by 2,3-benzodiazepines
-
Wilding, T.J. and Huettner, J.E., Differential antagonism of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-preferring and kainatepreferring receptors by 2,3-benzodiazepines, Mol. Pharmacol., 47 (1995) 582-587.
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 582-587
-
-
Wilding, T.J.1
Huettner, J.E.2
-
39
-
-
0029924437
-
Antagonist pharmacology of kainate- and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-preferring receptors
-
Wilding, T.J. and Huettner, J.E., Antagonist pharmacology of kainate- and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-preferring receptors, Mol. Pharmacol., 49 (1996) 540-546.
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 540-546
-
-
Wilding, T.J.1
Huettner, J.E.2
-
40
-
-
0028916586
-
Vitro pharmacology of ACEA-1021 and ACEA-1031: Systemically active quinoxalinediones with high affinity and selectivity for N-methyl-D-aspartate receptor glycine sites
-
Woodward, R.M., Huettner, J.E., Guastella, J., Keana, J.F.W. and Weber, E., In vitro pharmacology of ACEA-1021 and ACEA-1031: systemically active quinoxalinediones with high affinity and selectivity for N-methyl-D-aspartate receptor glycine sites, Mol. Pharmacol., 47 (1995) 568-581.
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 568-581
-
-
Woodward, R.M.1
Huettner, J.E.2
Guastella, J.3
Keana, J.F.W.4
Weber, E.5
-
41
-
-
0019775230
-
Spinal opiate analgesia: Characteristics and principles of action
-
Yaksh, T.L., Spinal opiate analgesia: characteristics and principles of action, Pain, 11 (1981) 293-346.
-
(1981)
Pain
, vol.11
, pp. 293-346
-
-
Yaksh, T.L.1
-
42
-
-
0023829817
-
Pharmacology of the allodynia in rats evoked by high dose intrathecal morphine
-
Yaksh, T.L. and Harty, G.J., Pharmacology of the allodynia in rats evoked by high dose intrathecal morphine, J. Pharmacol. Exp. Ther., 244 (1988) 501-507.
-
(1988)
J. Pharmacol. Exp. Ther.
, vol.244
, pp. 501-507
-
-
Yaksh, T.L.1
Harty, G.J.2
-
43
-
-
0022558928
-
High doses of spinal morphine produce a non-opiate receptor-mediated hyperesthesia: Clinical and theoretic implications
-
Yaksh, T.L., Harty, G.J. and Onofrio, B.M., High doses of spinal morphine produce a non-opiate receptor-mediated hyperesthesia: clinical and theoretic implications, Anesthesiology, 64 (1986) 590-597.
-
(1986)
Anesthesiology
, vol.64
, pp. 590-597
-
-
Yaksh, T.L.1
Harty, G.J.2
Onofrio, B.M.3
-
44
-
-
0026629818
-
Comparison of the antinociceptive effects of pre- and post-treatment with intrathecal morphine and MK-801, an NMDA antagonist, on the formalin test in the rat
-
Yamamoto, T. and Yaksh, T.L., Comparison of the antinociceptive effects of pre- and post-treatment with intrathecal morphine and MK-801, an NMDA antagonist, on the formalin test in the rat, Anesthesiology, 77 (1992) 757-765.
-
(1992)
Anesthesiology
, vol.77
, pp. 757-765
-
-
Yamamoto, T.1
Yaksh, T.L.2
-
45
-
-
0025189720
-
Tolerance develops to spinal morphine analgesia but not morphine-induced convulsions
-
Yoburn, B.C., Lutfy, K., Sierra, V. and Tortella, F.C., Tolerance develops to spinal morphine analgesia but not morphine-induced convulsions, Eur. J. Pharmacol., 176 (1990) 63-67.
-
(1990)
Eur. J. Pharmacol.
, vol.176
, pp. 63-67
-
-
Yoburn, B.C.1
Lutfy, K.2
Sierra, V.3
Tortella, F.C.4
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