-
1
-
-
0024333178
-
Behavioral evidence for a bidirectional effect of systemic naloxone in a model of experimental neuropathy in the rat
-
Attal N., Kayser V., Jazat F., and Guilbaud G. Behavioral evidence for a bidirectional effect of systemic naloxone in a model of experimental neuropathy in the rat. Brain Res. 494 (1989) 276-284
-
(1989)
Brain Res.
, vol.494
, pp. 276-284
-
-
Attal, N.1
Kayser, V.2
Jazat, F.3
Guilbaud, G.4
-
2
-
-
0022568647
-
Immunoreactive dynorphin B in sacral primary afferent fibers of the cat
-
Basbaum A.I., Cruz L., and Weber E. Immunoreactive dynorphin B in sacral primary afferent fibers of the cat. J. Neurosci. 6 (1986) 127-133
-
(1986)
J. Neurosci.
, vol.6
, pp. 127-133
-
-
Basbaum, A.I.1
Cruz, L.2
Weber, E.3
-
3
-
-
0025761623
-
Opioid control of the release of Met-enkephalin-like material from the rat spinal cord
-
Bourgoin S., Collin E., Benoliel J.J., Chantrel D., Mauborgne A., Pohl M., Hamon M., and Cesselin F. Opioid control of the release of Met-enkephalin-like material from the rat spinal cord. Brain Res. 551 (1991) 178-184
-
(1991)
Brain Res.
, vol.551
, pp. 178-184
-
-
Bourgoin, S.1
Collin, E.2
Benoliel, J.J.3
Chantrel, D.4
Mauborgne, A.5
Pohl, M.6
Hamon, M.7
Cesselin, F.8
-
4
-
-
0025079204
-
Stimulation of hypothalamic opioid peptide release by lithium is mediated by opioid autoreceptors: evidence from a combined in vitro, ex vivo study
-
Burns G., Herz A., and Nikolarakis K.E. Stimulation of hypothalamic opioid peptide release by lithium is mediated by opioid autoreceptors: evidence from a combined in vitro, ex vivo study. Neuroscience 36 (1990) 691-697
-
(1990)
Neuroscience
, vol.36
, pp. 691-697
-
-
Burns, G.1
Herz, A.2
Nikolarakis, K.E.3
-
5
-
-
0345035480
-
Evidence for opiate-activated NMDA processes masking opiate analgesia in rats
-
Celerier E., Laulin L.-P., Larcher A., Le Moal M., and Simonnet G. Evidence for opiate-activated NMDA processes masking opiate analgesia in rats. Brain Res. 847 (1999) 18-25
-
(1999)
Brain Res.
, vol.847
, pp. 18-25
-
-
Celerier, E.1
Laulin, L.-P.2
Larcher, A.3
Le Moal, M.4
Simonnet, G.5
-
6
-
-
0025060239
-
Opioids can evoke direct receptor-mediated excitatory effects on sensory neurons
-
Crain S.M., and Shen K.-F. Opioids can evoke direct receptor-mediated excitatory effects on sensory neurons. Trends Pharmacol. Sci. 11 (1990) 77-81
-
(1990)
Trends Pharmacol. Sci.
, vol.11
, pp. 77-81
-
-
Crain, S.M.1
Shen, K.-F.2
-
7
-
-
0026508677
-
After chronic opioid exposure sensory neurons become supersensitive to the excitatory effects of opioid agonists and antagonists as occurs after acute elevation of GM1 ganglioside
-
Crain S.M., and Shen K.-F. After chronic opioid exposure sensory neurons become supersensitive to the excitatory effects of opioid agonists and antagonists as occurs after acute elevation of GM1 ganglioside. Brain Res. 575 (1992) 13-24
-
(1992)
Brain Res.
, vol.575
, pp. 13-24
-
-
Crain, S.M.1
Shen, K.-F.2
-
8
-
-
0026567332
-
After GM1 ganglioside treatment of sensory neurons naloxone paradoxically prolongs the action potential but still antagonizes opioid inhibition
-
Crain S.M., and Shen K.-F. After GM1 ganglioside treatment of sensory neurons naloxone paradoxically prolongs the action potential but still antagonizes opioid inhibition. J. Pharmacol. Exp. Ther. 260 (1992) 182-186
-
(1992)
J. Pharmacol. Exp. Ther.
, vol.260
, pp. 182-186
-
-
Crain, S.M.1
Shen, K.-F.2
-
9
-
-
0028804902
-
Ultra-low concentrations of naloxone selectively antagonize excitatory effects of morphine on sensory neurons, thereby increasing its antinociceptive potency and attenuating tolerance/dependence during chronic co-treatment
-
Crain S.M., and Shen K.-F. Ultra-low concentrations of naloxone selectively antagonize excitatory effects of morphine on sensory neurons, thereby increasing its antinociceptive potency and attenuating tolerance/dependence during chronic co-treatment. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 10540-10544
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 10540-10544
-
-
Crain, S.M.1
Shen, K.-F.2
-
10
-
-
0029163514
-
Chronic morphine-treated sensory ganglion neurons remain supersensitive to the excitatory effects of naloxone for months after return to normal culture medium: an in vitro model of 'protracted opioid dependence'
-
Crain S.M., and Shen K.-F. Chronic morphine-treated sensory ganglion neurons remain supersensitive to the excitatory effects of naloxone for months after return to normal culture medium: an in vitro model of 'protracted opioid dependence'. Brain Res. 694 (1995) 103-110
-
(1995)
Brain Res.
, vol.694
, pp. 103-110
-
-
Crain, S.M.1
Shen, K.-F.2
-
11
-
-
0031712776
-
Modulation of opioid analgesia, tolerance and dependence by Gs-coupled, GM1 ganglioside-regulated opioid receptor functions
-
Crain S.M., and Shen K.-F. Modulation of opioid analgesia, tolerance and dependence by Gs-coupled, GM1 ganglioside-regulated opioid receptor functions. Trends Pharmacol. Sci. 19 (1998) 358-365
-
(1998)
Trends Pharmacol. Sci.
, vol.19
, pp. 358-365
-
-
Crain, S.M.1
Shen, K.-F.2
-
12
-
-
0031904516
-
GM1 ganglioside-induced modulation of opioid receptor-mediated functions
-
Crain S.M., and Shen K.-F. GM1 ganglioside-induced modulation of opioid receptor-mediated functions. Ann. N.Y. Acad. Sci. 845 (1998) 106-125
-
(1998)
Ann. N.Y. Acad. Sci.
, vol.845
, pp. 106-125
-
-
Crain, S.M.1
Shen, K.-F.2
-
13
-
-
0033953224
-
Enhanced analgesic potency and reduced tolerance of morphine in 129/SvEv mice: evidence for a deficiency in GM1 ganglioside-regulated excitatory opioid receptor functions
-
Crain S.M., and Shen K.-F. Enhanced analgesic potency and reduced tolerance of morphine in 129/SvEv mice: evidence for a deficiency in GM1 ganglioside-regulated excitatory opioid receptor functions. Brain Res. 856 (2000) 227-235
-
(2000)
Brain Res.
, vol.856
, pp. 227-235
-
-
Crain, S.M.1
Shen, K.-F.2
-
14
-
-
0033957306
-
Antagonists of excitatory opioid receptor functions enhance morphine's analgesic potency and attenuate opioid tolerance/dependence liability
-
Crain S.M., and Shen K.-F. Antagonists of excitatory opioid receptor functions enhance morphine's analgesic potency and attenuate opioid tolerance/dependence liability. Pain 84 (2000) 121-131
-
(2000)
Pain
, vol.84
, pp. 121-131
-
-
Crain, S.M.1
Shen, K.-F.2
-
15
-
-
0035808569
-
Acute thermal hyperalgesia elicited by low-dose morphine in normal mice is blocked by ultra-low naltrexone, unmasking potent opioid analgesia
-
Crain S.M., and Shen K.-F. Acute thermal hyperalgesia elicited by low-dose morphine in normal mice is blocked by ultra-low naltrexone, unmasking potent opioid analgesia. Brain Res. 888 (2001) 75-82
-
(2001)
Brain Res.
, vol.888
, pp. 75-82
-
-
Crain, S.M.1
Shen, K.-F.2
-
16
-
-
0346221268
-
Neuraminidase inhibitor, oseltamivir blocks GM1 ganglioside-regulated excitatory opioid receptor-mediated hyperalgesia, enhances opioid analgesia and attenuates tolerance in mice
-
Crain S.M., and Shen K.-F. Neuraminidase inhibitor, oseltamivir blocks GM1 ganglioside-regulated excitatory opioid receptor-mediated hyperalgesia, enhances opioid analgesia and attenuates tolerance in mice. Brain Res. 995 (2004) 260-266
-
(2004)
Brain Res.
, vol.995
, pp. 260-266
-
-
Crain, S.M.1
Shen, K.-F.2
-
17
-
-
0021268356
-
Analgesic effects of kelatorphan, a new highly potent inhibitor of multiple enkephalin degrading enzymes
-
Fournie-Zaluski M.C., Chaillet P., Bouboutou R., Coulaud A., Cherot P., Waksman G., Costentin J., and Roques B.P. Analgesic effects of kelatorphan, a new highly potent inhibitor of multiple enkephalin degrading enzymes. Eur. J. Pharmacol. 102 (1984) 525-528
-
(1984)
Eur. J. Pharmacol.
, vol.102
, pp. 525-528
-
-
Fournie-Zaluski, M.C.1
Chaillet, P.2
Bouboutou, R.3
Coulaud, A.4
Cherot, P.5
Waksman, G.6
Costentin, J.7
Roques, B.P.8
-
18
-
-
33646288893
-
Nalorphine: increased sensitivity of monkeys formerly dependent on morphine
-
Goldberg S.R., and Schuster C.R. Nalorphine: increased sensitivity of monkeys formerly dependent on morphine. Science 166 (1969) 1548-1549
-
(1969)
Science
, vol.166
, pp. 1548-1549
-
-
Goldberg, S.R.1
Schuster, C.R.2
-
19
-
-
34548110920
-
Phenotypic changes induced in dorsal root ganglion neurons by nerve injury
-
Opioid Sensitivity of Chronic Noncancer Pain. Kalso E., McQuay H.J., and Wiesenfeld-Hallin Z. (Eds), IASP Press, Seattle
-
Hökfelt T., Shi T.-J.S., Cui J.-G., Meyerson B., Linderoth B., Tong Y.-G., Wang H.F., Xu Z.-Q.D., Ju G., Grant G., and Zhang X. Phenotypic changes induced in dorsal root ganglion neurons by nerve injury. In: Kalso E., McQuay H.J., and Wiesenfeld-Hallin Z. (Eds). Opioid Sensitivity of Chronic Noncancer Pain. Progress in Pain Research and Management vol. 14 (1999), IASP Press, Seattle 145-161
-
(1999)
Progress in Pain Research and Management
, vol.14
, pp. 145-161
-
-
Hökfelt, T.1
Shi, T.-J.S.2
Cui, J.-G.3
Meyerson, B.4
Linderoth, B.5
Tong, Y.-G.6
Wang, H.F.7
Xu, Z.-Q.D.8
Ju, G.9
Grant, G.10
Zhang, X.11
-
21
-
-
0021234314
-
Acute and chronic morphine modifies the in vivo release of methionine enkephalin-like immunoreactivity from the cat spinal cord and brain
-
Jhamandas K., Yaksh T.L., and Go V.L.W. Acute and chronic morphine modifies the in vivo release of methionine enkephalin-like immunoreactivity from the cat spinal cord and brain. Brain Res. 297 (1984) 91-103
-
(1984)
Brain Res.
, vol.297
, pp. 91-103
-
-
Jhamandas, K.1
Yaksh, T.L.2
Go, V.L.W.3
-
22
-
-
0029881933
-
Spinal amino acid release and precipitated withdrawal in rats chronically infused with spinal morphine
-
Jhamandas K.H., Marsala M., Ibuki T., and Yaksh T.L. Spinal amino acid release and precipitated withdrawal in rats chronically infused with spinal morphine. J. Neurosci. 16 (1996) 2758-2766
-
(1996)
J. Neurosci.
, vol.16
, pp. 2758-2766
-
-
Jhamandas, K.H.1
Marsala, M.2
Ibuki, T.3
Yaksh, T.L.4
-
23
-
-
0025259677
-
Mu antagonist and kappa agonist properties of β-funaltrexamine (β-FNA) in vivo: long-lasting spinal analgesia in mice
-
Jiang Q., Heyman J.S., Sheldon R.J., Koslo J., and Porreca F. Mu antagonist and kappa agonist properties of β-funaltrexamine (β-FNA) in vivo: long-lasting spinal analgesia in mice. J. Pharmacol. Exp. Ther. 252 (1990) 1006-1011
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.252
, pp. 1006-1011
-
-
Jiang, Q.1
Heyman, J.S.2
Sheldon, R.J.3
Koslo, J.4
Porreca, F.5
-
24
-
-
0019843730
-
Dose-dependent analgesic and hyperalgesic effects of systemic naloxone in arthritic rats
-
Kayser V., and Guilbaud G. Dose-dependent analgesic and hyperalgesic effects of systemic naloxone in arthritic rats. Brain Res. 226 (1981) 344-348
-
(1981)
Brain Res.
, vol.226
, pp. 344-348
-
-
Kayser, V.1
Guilbaud, G.2
-
25
-
-
0022446913
-
Analgesia produced by low doses of the opiate antagonist naloxone in arthritic rats is reduced in morphine-tolerant animals
-
Kayser V., Besson J.M., and Guilbaud G. Analgesia produced by low doses of the opiate antagonist naloxone in arthritic rats is reduced in morphine-tolerant animals. Brain Res. 371 (1986) 37-41
-
(1986)
Brain Res.
, vol.371
, pp. 37-41
-
-
Kayser, V.1
Besson, J.M.2
Guilbaud, G.3
-
26
-
-
0023698602
-
Behavioural and electrophysiological studies on the paradoxical antinociceptive effects of an extremely low dose of naloxone in an animal model of acute and localized inflammation
-
Kayser V., Benoist J.M., Neil A., Gautron M., and Guilbaud G. Behavioural and electrophysiological studies on the paradoxical antinociceptive effects of an extremely low dose of naloxone in an animal model of acute and localized inflammation. Exp. Brain Res. 73 (1988) 402-410
-
(1988)
Exp. Brain Res.
, vol.73
, pp. 402-410
-
-
Kayser, V.1
Benoist, J.M.2
Neil, A.3
Gautron, M.4
Guilbaud, G.5
-
27
-
-
0024452914
-
Potent antinociceptive effects of kelatorphan (a highly efficient inhibitor of multiple enkephalin degrading enzymes) systemically administered in normal and arthritic rats
-
Kayser V., Fournie-Zaluski M.C., Guilbaud G., and Roques B.P. Potent antinociceptive effects of kelatorphan (a highly efficient inhibitor of multiple enkephalin degrading enzymes) systemically administered in normal and arthritic rats. Brain Res. 497 (1989) 94-101
-
(1989)
Brain Res.
, vol.497
, pp. 94-101
-
-
Kayser, V.1
Fournie-Zaluski, M.C.2
Guilbaud, G.3
Roques, B.P.4
-
28
-
-
0025333160
-
Morphine analgesia and acute physical dependence: rapid onset of two opposing, dose-related processes
-
Kim D.H., Fields H.L., and Barbaro N.M. Morphine analgesia and acute physical dependence: rapid onset of two opposing, dose-related processes. Brain Res. 516 (1990) 37-40
-
(1990)
Brain Res.
, vol.516
, pp. 37-40
-
-
Kim, D.H.1
Fields, H.L.2
Barbaro, N.M.3
-
29
-
-
0019116111
-
Presynaptic regulation of the release of catecholamines
-
Langer S.Z. Presynaptic regulation of the release of catecholamines. Pharmacol. Rev. 32 (1981) 337-362
-
(1981)
Pharmacol. Rev.
, vol.32
, pp. 337-362
-
-
Langer, S.Z.1
-
30
-
-
0031003160
-
25 years since the discovery of presynaptic receptors: present knowledge and future perspectives
-
Langer S.Z. 25 years since the discovery of presynaptic receptors: present knowledge and future perspectives. Trends Pharmacol. Sci. 18 (1997) 95-99
-
(1997)
Trends Pharmacol. Sci.
, vol.18
, pp. 95-99
-
-
Langer, S.Z.1
-
31
-
-
0029162234
-
Mechanisms of hyperalgesia and morphine tolerance: a current view of their possible interactions
-
Mao J., Price D.D., and Mayer D.J. Mechanisms of hyperalgesia and morphine tolerance: a current view of their possible interactions. Pain 62 (1995) 259-274
-
(1995)
Pain
, vol.62
, pp. 259-274
-
-
Mao, J.1
Price, D.D.2
Mayer, D.J.3
-
32
-
-
0036830646
-
From neurobiology to treatment: progress against addiction
-
Nestler E.J. From neurobiology to treatment: progress against addiction. Nat. Neurosci. Suppl. 5 (2002) 1076-1079
-
(2002)
Nat. Neurosci.
, vol.SUPPL. 5
, pp. 1076-1079
-
-
Nestler, E.J.1
-
33
-
-
0024411615
-
Presynaptic auto- and allelo-receptor regulation of hypothalamic opioid peptide release
-
Nikolarakis K.E., Almeida O.F.X., Yassouridis A., and Herz A. Presynaptic auto- and allelo-receptor regulation of hypothalamic opioid peptide release. Neuroscience 31 (1989) 269-273
-
(1989)
Neuroscience
, vol.31
, pp. 269-273
-
-
Nikolarakis, K.E.1
Almeida, O.F.X.2
Yassouridis, A.3
Herz, A.4
-
34
-
-
0026704581
-
Inhibition of the enkephalin-metabolizing enzymes by the first systemically active mixed inhibitor prodrug RB101 induces potent analgesic responses in mice and rats
-
Noble F., Soleilhac J.M., Soroca-Lucas E., Turcaud S., Fournie-Zaluski M.C., and Roques B.P. Inhibition of the enkephalin-metabolizing enzymes by the first systemically active mixed inhibitor prodrug RB101 induces potent analgesic responses in mice and rats. J. Pharmacol. Exp. Ther. 261 (1992) 181-190
-
(1992)
J. Pharmacol. Exp. Ther.
, vol.261
, pp. 181-190
-
-
Noble, F.1
Soleilhac, J.M.2
Soroca-Lucas, E.3
Turcaud, S.4
Fournie-Zaluski, M.C.5
Roques, B.P.6
-
35
-
-
0028222694
-
Paradoxical analgesia induced by low doses of naloxone is not potentiated by complete inhibition of enkephalin degradation
-
Noble F., Fournie-Zaluski M.C., and Roques B.P. Paradoxical analgesia induced by low doses of naloxone is not potentiated by complete inhibition of enkephalin degradation. Neuropharmacology 33 (1994) 135-140
-
(1994)
Neuropharmacology
, vol.33
, pp. 135-140
-
-
Noble, F.1
Fournie-Zaluski, M.C.2
Roques, B.P.3
-
36
-
-
0022638545
-
Opioid receptor types and membrane ion channels
-
North R.A. Opioid receptor types and membrane ion channels. Trends Neurosci. 9 (1986) 114-117
-
(1986)
Trends Neurosci.
, vol.9
, pp. 114-117
-
-
North, R.A.1
-
37
-
-
20444391553
-
Ultra-low-dose naltrexone suppresses rewarding effects of opiates and aversive effects of opiate withdrawal in rats
-
Olmstead M.C., and Burns L.H. Ultra-low-dose naltrexone suppresses rewarding effects of opiates and aversive effects of opiate withdrawal in rats. Psychopharmacology 181 (2005) 576-581
-
(2005)
Psychopharmacology
, vol.181
, pp. 576-581
-
-
Olmstead, M.C.1
Burns, L.H.2
-
39
-
-
0036156508
-
Paradoxical effects of the opioid antagonist naltrexone on morphine analgesia, tolerance, and reward in rats
-
Powell K.J., Abul-Husn N.S., Jhamandas A., Olmstead M.C., Beninger R.J., and Jhamandas K. Paradoxical effects of the opioid antagonist naltrexone on morphine analgesia, tolerance, and reward in rats. J. Pharmacol. Exp. Ther. 300 (2002) 588-596
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.300
, pp. 588-596
-
-
Powell, K.J.1
Abul-Husn, N.S.2
Jhamandas, A.3
Olmstead, M.C.4
Beninger, R.J.5
Jhamandas, K.6
-
40
-
-
0021288907
-
Multiple mechanisms of withdrawal from opioid drugs
-
Redmond Jr. D.E., and Krystal J.H. Multiple mechanisms of withdrawal from opioid drugs. Ann. Rev. Neurosci. 7 (1984) 443-478
-
(1984)
Ann. Rev. Neurosci.
, vol.7
, pp. 443-478
-
-
Redmond Jr., D.E.1
Krystal, J.H.2
-
41
-
-
0022479640
-
Direct demonstration of the activation of UDP-N-acetylgalactosamine:[GM3]N-acetylgalactosaminyltransferase by cyclic AMP
-
Scheideler M.A., and Dawson G. Direct demonstration of the activation of UDP-N-acetylgalactosamine:[GM3]N-acetylgalactosaminyltransferase by cyclic AMP. J. Neurochem. 46 (1986) 1639-1643
-
(1986)
J. Neurochem.
, vol.46
, pp. 1639-1643
-
-
Scheideler, M.A.1
Dawson, G.2
-
42
-
-
0024341553
-
Dual opioid modulation of the action potential duration of mouse dorsal root ganglion neurons in culture
-
Shen K.-F., and Crain S.M. Dual opioid modulation of the action potential duration of mouse dorsal root ganglion neurons in culture. Brain Res. 491 (1989) 227-242
-
(1989)
Brain Res.
, vol.491
, pp. 227-242
-
-
Shen, K.-F.1
Crain, S.M.2
-
43
-
-
0025032287
-
Cholera toxin-A subunit blocks opioid excitatory effects on sensory neuron action potentials indicating mediation by Gs-linked opioid receptors
-
Shen K.-F., and Crain S.M. Cholera toxin-A subunit blocks opioid excitatory effects on sensory neuron action potentials indicating mediation by Gs-linked opioid receptors. Brain Res. 525 (1990) 225-231
-
(1990)
Brain Res.
, vol.525
, pp. 225-231
-
-
Shen, K.-F.1
Crain, S.M.2
-
44
-
-
0025039134
-
Cholera toxin-B subunit blocks opioid excitatory effects on sensory neuron action potentials indicating that GM1 ganglioside may regulate Gs-linked opioid receptor functions
-
Shen K.-F., and Crain S.M. Cholera toxin-B subunit blocks opioid excitatory effects on sensory neuron action potentials indicating that GM1 ganglioside may regulate Gs-linked opioid receptor functions. Brain Res. 531 (1990) 1-7
-
(1990)
Brain Res.
, vol.531
, pp. 1-7
-
-
Shen, K.-F.1
Crain, S.M.2
-
45
-
-
0026470851
-
Chronic selective activation of excitatory opioid receptor functions in sensory neurons results in opioid "dependence" without tolerance
-
Shen K.-F., and Crain S.M. Chronic selective activation of excitatory opioid receptor functions in sensory neurons results in opioid "dependence" without tolerance. Brain Res. 597 (1992) 74-83
-
(1992)
Brain Res.
, vol.597
, pp. 74-83
-
-
Shen, K.-F.1
Crain, S.M.2
-
46
-
-
0028088135
-
Nerve growth factor rapidly prolongs the action potential of mature sensory neurons in culture and this effect requires activation of Gs-coupled excitatory kappa opioid receptors on these cells
-
Shen K.-F., and Crain S.M. Nerve growth factor rapidly prolongs the action potential of mature sensory neurons in culture and this effect requires activation of Gs-coupled excitatory kappa opioid receptors on these cells. J. Neurosci. 14 (1994) 5570-5579
-
(1994)
J. Neurosci.
, vol.14
, pp. 5570-5579
-
-
Shen, K.-F.1
Crain, S.M.2
-
47
-
-
0030945699
-
Ultra-low doses of naltrexone or etorphine increase morphine's antinociceptive potency and attenuate tolerance/dependence in mice
-
Shen K.-F., and Crain S.M. Ultra-low doses of naltrexone or etorphine increase morphine's antinociceptive potency and attenuate tolerance/dependence in mice. Brain Res. 757 (1997) 176-190
-
(1997)
Brain Res.
, vol.757
, pp. 176-190
-
-
Shen, K.-F.1
Crain, S.M.2
-
48
-
-
0035900180
-
Cholera toxin-B subunit blocks excitatory opioid receptor-mediated hyperalgesic effects in mice, thereby unmasking potent opioid analgesia and attenuating opioid tolerance/dependence
-
Shen K.-F., and Crain S.M. Cholera toxin-B subunit blocks excitatory opioid receptor-mediated hyperalgesic effects in mice, thereby unmasking potent opioid analgesia and attenuating opioid tolerance/dependence. Brain Res. 919 (2001) 20-30
-
(2001)
Brain Res.
, vol.919
, pp. 20-30
-
-
Shen, K.-F.1
Crain, S.M.2
-
49
-
-
0026066546
-
Brief treatment of sensory ganglion neurons with GM1 ganglioside enhances the efficacy of opioid excitatory effects on the action potential
-
Shen K.-F., Crain S.M., and Ledeen R.W. Brief treatment of sensory ganglion neurons with GM1 ganglioside enhances the efficacy of opioid excitatory effects on the action potential. Brain Res. 550 (1991) 130-138
-
(1991)
Brain Res.
, vol.550
, pp. 130-138
-
-
Shen, K.-F.1
Crain, S.M.2
Ledeen, R.W.3
-
50
-
-
0024347556
-
Modulation of neurotransmitter release by presynaptic autoreceptors
-
Starke K., Gothert M., and Kilbinger H. Modulation of neurotransmitter release by presynaptic autoreceptors. Physiol. Rev. 69 (1989) 864-989
-
(1989)
Physiol. Rev.
, vol.69
, pp. 864-989
-
-
Starke, K.1
Gothert, M.2
Kilbinger, H.3
-
52
-
-
0015549995
-
Hyperalgesia during withdrawal as a means of measuring the degree of dependence in morphine dependent rats
-
Tilson H.A., Rech R.H., and Stolman S. Hyperalgesia during withdrawal as a means of measuring the degree of dependence in morphine dependent rats. Psychopharmacologia 28 (1973) 287-300
-
(1973)
Psychopharmacologia
, vol.28
, pp. 287-300
-
-
Tilson, H.A.1
Rech, R.H.2
Stolman, S.3
-
53
-
-
0033535120
-
Increased uptake and transport of cholera toxin B-subunit in dorsal root ganglion neurons after peripheral axotomy: possible implications for sensory sprouting
-
Tong Y.-G., Wang H.F., Ju G., Grant G., Hökfelt T., and Zhang X. Increased uptake and transport of cholera toxin B-subunit in dorsal root ganglion neurons after peripheral axotomy: possible implications for sensory sprouting. J. Comp. Neurol. 404 (1999) 143-158
-
(1999)
J. Comp. Neurol.
, vol.404
, pp. 143-158
-
-
Tong, Y.-G.1
Wang, H.F.2
Ju, G.3
Grant, G.4
Hökfelt, T.5
Zhang, X.6
-
54
-
-
0022616622
-
Low doses of naloxone produce analgesia in the mouse brain by blocking presynaptic autoinhibition of enkephalin release
-
Ueda H., Fukushima N., Kitao T., Ge M., and Takagi H. Low doses of naloxone produce analgesia in the mouse brain by blocking presynaptic autoinhibition of enkephalin release. Neurosci. Lett. 65 (1986) 247-252
-
(1986)
Neurosci. Lett.
, vol.65
, pp. 247-252
-
-
Ueda, H.1
Fukushima, N.2
Kitao, T.3
Ge, M.4
Takagi, H.5
-
55
-
-
0023634848
-
Presynaptic opioid kappa-receptor and regulation of the release of met-enkephalin in the rat brainstem
-
Ueda H., Fukushima N., Ge M., Takagi H., and Satoh M. Presynaptic opioid kappa-receptor and regulation of the release of met-enkephalin in the rat brainstem. Neurosci. Lett. 81 (1987) 309-313
-
(1987)
Neurosci. Lett.
, vol.81
, pp. 309-313
-
-
Ueda, H.1
Fukushima, N.2
Ge, M.3
Takagi, H.4
Satoh, M.5
-
57
-
-
33750807737
-
Gβγ that interacts with adenylyl cyclase in opioid tolerance originates from a Gs protein
-
Wang H.-Y., and Burns L.H. Gβγ that interacts with adenylyl cyclase in opioid tolerance originates from a Gs protein. J. Neurobiol. 66 (2006) 1302-1310
-
(2006)
J. Neurobiol.
, vol.66
, pp. 1302-1310
-
-
Wang, H.-Y.1
Burns, L.H.2
-
58
-
-
20444375332
-
Ultra-low-dose naloxone suppresses opioid tolerance, dependence and associated changes in mu opioid receptor-G protein coupling and Gβγ signaling
-
Wang H.-Y., Friedman E., Olmstead M.C., and Burns L.H. Ultra-low-dose naloxone suppresses opioid tolerance, dependence and associated changes in mu opioid receptor-G protein coupling and Gβγ signaling. Neuroscience 135 (2005) 247-261
-
(2005)
Neuroscience
, vol.135
, pp. 247-261
-
-
Wang, H.-Y.1
Friedman, E.2
Olmstead, M.C.3
Burns, L.H.4
-
59
-
-
0020684011
-
Relative involvement of mu, kappa and delta receptor mechanisms in opiate-mediated antinociception in mice
-
Ward S.J., and Takemori A.E. Relative involvement of mu, kappa and delta receptor mechanisms in opiate-mediated antinociception in mice. J. Pharmacol. Exp. Ther. 224 (1983) 525-530
-
(1983)
J. Pharmacol. Exp. Ther.
, vol.224
, pp. 525-530
-
-
Ward, S.J.1
Takemori, A.E.2
-
60
-
-
0020051193
-
Pharmacological characterization in vivo of the novel opiate, β-funaltrexamine
-
Ward S.J., Portoghese P.S., and Takemori A.E. Pharmacological characterization in vivo of the novel opiate, β-funaltrexamine. J. Pharmacol. Exp. Ther. 220 (1982) 494-498
-
(1982)
J. Pharmacol. Exp. Ther.
, vol.220
, pp. 494-498
-
-
Ward, S.J.1
Portoghese, P.S.2
Takemori, A.E.3
-
63
-
-
0031039056
-
Interaction of δ-opioid receptor with GM1 ganglioside: conversion from inhibitory to excitatory mode
-
Wu G., Lu Z.-H., and Ledeen R.W. Interaction of δ-opioid receptor with GM1 ganglioside: conversion from inhibitory to excitatory mode. Mol. Brain Res. 44 (1997) 341-346
-
(1997)
Mol. Brain Res.
, vol.44
, pp. 341-346
-
-
Wu, G.1
Lu, Z.-H.2
Ledeen, R.W.3
-
64
-
-
0031904517
-
The role of GM1 ganglioside in regulating excitatory opioid effects
-
Wu G., Lu Z.-H., Tzongjer J.W., Howells R.D., Christoffers K., and Ledeen R.W. The role of GM1 ganglioside in regulating excitatory opioid effects. Ann. N.Y. Acad. Sci. 845 (1998) 126-138
-
(1998)
Ann. N.Y. Acad. Sci.
, vol.845
, pp. 126-138
-
-
Wu, G.1
Lu, Z.-H.2
Tzongjer, J.W.3
Howells, R.D.4
Christoffers, K.5
Ledeen, R.W.6
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