-
1
-
-
0038460075
-
A new view of pain as a homeostatic emotion
-
Craig AD. A new view of pain as a homeostatic emotion. Trends Neurosci 2003; 26: 303-7.
-
(2003)
Trends Neurosci
, vol.26
, pp. 303-307
-
-
Craig, A.D.1
-
2
-
-
0035855860
-
Molecular mechanisms of nociception
-
Julius D, Basbaum Al. Molecular mechanisms of nociception. Nature 2001; 413: 203-10.
-
(2001)
Nature
, vol.413
, pp. 203-210
-
-
Julius, D.1
Basbaum, Al.2
-
3
-
-
0038082928
-
Pain mechanisms: Labeled lines versus convergence in central processing
-
Craig AD. Pain mechanisms: labeled lines versus convergence in central processing. Annu Rev Neurosci 2003; 26: 1-30.
-
(2003)
Annu Rev Neurosci
, vol.26
, pp. 1-30
-
-
Craig, A.D.1
-
5
-
-
0032778263
-
Ion channels in presynaptic nerve terminals and control of transmitter release
-
Meir A, Ginsburg S, Butkevich A, et al. Ion channels in presynaptic nerve terminals and control of transmitter release. Physiol Rev 1999; 79: 1019-88.
-
(1999)
Physiol Rev
, vol.79
, pp. 1019-1088
-
-
Meir, A.1
Ginsburg, S.2
Butkevich, A.3
-
6
-
-
0033713292
-
Nomenclature of voltage-gated calcium channels
-
Ertel EA, Campbell KP, Harpold MM, et al. Nomenclature of voltage-gated calcium channels. Neuron 2000; 25: 533-5.
-
(2000)
Neuron
, vol.25
, pp. 533-535
-
-
Ertel, E.A.1
Campbell, K.P.2
Harpold, M.M.3
-
9
-
-
0021242718
-
A venom peptide with a novel presynaptic blocking action
-
Kerr LM, Yoshikami D. A venom peptide with a novel presynaptic blocking action. Nature 1984; 308: 282-4.
-
(1984)
Nature
, vol.308
, pp. 282-284
-
-
Kerr, L.M.1
Yoshikami, D.2
-
10
-
-
0023187486
-
Neuronal calcium channel antagonists. Discrimination between calcium channel subtypes using omega-conotoxin from Conus magus venom
-
Olivera BM, Cruz LJ, de Santos V, et al. Neuronal calcium channel antagonists. Discrimination between calcium channel subtypes using omega-conotoxin from Conus magus venom. Biochemistry 1987; 26: 2086-90.
-
(1987)
Biochemistry
, vol.26
, pp. 2086-2090
-
-
Olivera, B.M.1
Cruz, L.J.2
De Santos, V.3
-
11
-
-
0028836065
-
Effect of continuous intrathecal infusion of omega-conopeptides, N-type calcium-channel blockers, on behavior and antinociception in the formalin and hot-plate tests in rats
-
Malmberg AB, Yaksh TL. Effect of continuous intrathecal infusion of omega-conopeptides, N-type calcium-channel blockers, on behavior and antinociception in the formalin and hot-plate tests in rats. Pain 1995; 60: 83-90.
-
(1995)
Pain
, vol.60
, pp. 83-90
-
-
Malmberg, A.B.1
Yaksh, T.L.2
-
12
-
-
0028335910
-
Role of voltage-dependent calcium channel subtypes in experimental tactile allodynia
-
Chaplan SR, Pogrel JW, Vaksh TL. Role of voltage-dependent calcium channel subtypes in experimental tactile allodynia. J Pharmacol Exp Ther 1994; 269: 1117-23.
-
(1994)
J Pharmacol Exp Ther
, vol.269
, pp. 1117-1123
-
-
Chaplan, S.R.1
Pogrel, J.W.2
Vaksh, T.L.3
-
13
-
-
9144230737
-
Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS: A randomized controlled trial
-
Staats PS, Yearwood T, Charapata SG, et al. Intrathecal ziconotide in the treatment of refractory pain in patients with cancer or AIDS: a randomized controlled trial JAMA 2004; 291: 63-70.
-
(2004)
JAMA
, vol.291
, pp. 63-70
-
-
Staats, P.S.1
Yearwood, T.2
Charapata, S.G.3
-
14
-
-
0033952153
-
Adverse effects associated with the intrathecal administration of ziconotide
-
Penn RD, Paice JA. Adverse effects associated with the intrathecal administration of ziconotide. Pain 2000; 85: 291-6.
-
(2000)
Pain
, vol.85
, pp. 291-296
-
-
Penn, R.D.1
Paice, J.A.2
-
15
-
-
0037423378
-
Omega-conotoxin CVID inhibits a pharmacologically distinct voltage-sensitive calcium channel associated with transmitter release from preganglionic nerve terminals
-
Adams DJ, Smith AB, Schroeder CI, et al. Omega-conotoxin CVID inhibits a pharmacologically distinct voltage-sensitive calcium channel associated with transmitter release from preganglionic nerve terminals. J Biol Chem 2003; 278: 4057-62.
-
(2003)
J Biol Chem
, vol.278
, pp. 4057-4062
-
-
Adams, D.J.1
Smith, A.B.2
Schroeder, C.I.3
-
16
-
-
0036217174
-
The novel N-type calcium channel blocker, AM336, produces potent dose-dependent antinociception after intrathecal dosing in rats and inhibits substance P release in rat spinal cord slices
-
Smith MT, Cabot PJ, Ross FB, et al. The novel N-type calcium channel blocker, AM336, produces potent dose-dependent antinociception after intrathecal dosing in rats and inhibits substance P release in rat spinal cord slices. Pain 2002; 96: 119-27.
-
(2002)
Pain
, vol.96
, pp. 119-127
-
-
Smith, M.T.1
Cabot, P.J.2
Ross, F.B.3
-
17
-
-
14944380608
-
Synergy between intrathecal omega-conotoxin CVID and dexmedetomidine to attenuate mechanical hypersensitivity in the rat
-
Blake DW, Scott DA, Angus JA, Wright CE. Synergy between intrathecal omega-conotoxin CVID and dexmedetomidine to attenuate mechanical hypersensitivity in the rat. Eur J Pharmacol 2005; 506: 221-7.
-
(2005)
Eur J Pharmacol
, vol.506
, pp. 221-227
-
-
Blake, D.W.1
Scott, D.A.2
Angus, J.A.3
Wright, C.E.4
-
18
-
-
18344388289
-
Structure-activity study of L-cysteine-based N-type calcium channel blockers: Optimization of N- and C-terminal substituents
-
Seko T, Kato M, Kohno H, et al. Structure-activity study of L-cysteine-based N-type calcium channel blockers: optimization of N- and C-terminal substituents. Bioorg Med Chem Lett 2002; 12: 915-8.
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 915-918
-
-
Seko, T.1
Kato, M.2
Kohno, H.3
-
19
-
-
8644236608
-
Design, synthesis, and preliminary pharmacological evaluation of 4-aminopiperidine derivatives as N-type calcium channel blockers active on pain and neuropathic pain
-
Teodori E, Baldi E, Dei S, et al. Design, synthesis, and preliminary pharmacological evaluation of 4-aminopiperidine derivatives as N-type calcium channel blockers active on pain and neuropathic pain. J Med Chem 2004; 47: 6070-81.
-
(2004)
J Med Chem
, vol.47
, pp. 6070-6081
-
-
Teodori, E.1
Baldi, E.2
Dei, S.3
-
20
-
-
0347224274
-
Cell-specific alternative splicing increases calcium channel current density in the pain pathway
-
Bell TJ, Thaler C, Castiglioni AJ, et al. Cell-specific alternative splicing increases calcium channel current density in the pain pathway. Neuron 2004; 41: 127-38.
-
(2004)
Neuron
, vol.41
, pp. 127-138
-
-
Bell, T.J.1
Thaler, C.2
Castiglioni, A.J.3
-
21
-
-
0025869463
-
Mu-opioid-receptor-mediated inhibition of the N-type calcium-channel current
-
Seward E, Hammond C, Henderson G. Mu-opioid-receptor-mediated inhibition of the N-type calcium-channel current. Proc Biol Sci 1991; 244: 129-35.
-
(1991)
Proc Biol Sci
, vol.244
, pp. 129-135
-
-
Seward, E.1
Hammond, C.2
Henderson, G.3
-
22
-
-
0031033757
-
Direct binding of G-protein betagamma complex to voltage-dependent calcium channels
-
De Waard M, Liu H, Walker D, et al. Direct binding of G-protein betagamma complex to voltage-dependent calcium channels. Nature 1997; 385: 446-50.
-
(1997)
Nature
, vol.385
, pp. 446-450
-
-
De Waard, M.1
Liu, H.2
Walker, D.3
-
23
-
-
0031022543
-
Crosstalk between G proteins and protein kinase C mediated by the calcium channel alpha1 subunit
-
Zamponi GW, Bourinet E, Nelson D, et al. Crosstalk between G proteins and protein kinase C mediated by the calcium channel alpha1 subunit. nature 1997; 385: 442-6.
-
(1997)
Nature
, vol.385
, pp. 442-446
-
-
Zamponi, G.W.1
Bourinet, E.2
Nelson, D.3
-
24
-
-
17044380501
-
Spinal G-protein-gated potassium channels contribute in a dose-dependent manner to the analgesic effect of mu- and delta- but not kappa-opioids
-
Marker CL, Lujan R, Loh HH, Wickman K. Spinal G-protein-gated potassium channels contribute in a dose-dependent manner to the analgesic effect of mu- and delta- but not kappa-opioids J Neurosci 2005; 25: 3551-9.
-
(2005)
J Neurosci
, vol.25
, pp. 3551-3559
-
-
Marker, C.L.1
Lujan, R.2
Loh, H.H.3
Wickman, K.4
-
25
-
-
0037082324
-
Target validation of G-protein coupled receptors
-
Wise A, Gearing K, Rees S. Target validation of G-protein coupled receptors. Drug Discov Today 2002; 7: 235-46.
-
(2002)
Drug Discov Today
, vol.7
, pp. 235-246
-
-
Wise, A.1
Gearing, K.2
Rees, S.3
-
26
-
-
0031553387
-
Nociceptin/orphanin FQ and the opioid receptor-like ORL1 receptor
-
Meunier JC. Nociceptin/orphanin FQ and the opioid receptor-like ORL1 receptor. Eur J Pharmacol 1997; 340: 1-15.
-
(1997)
Eur J Pharmacol
, vol.340
, pp. 1-15
-
-
Meunier, J.C.1
-
27
-
-
9144233475
-
Agonist-independent modulation of N-type calcium channels by ORL1 receptors
-
Beedle AM, McRory JE, Poirot O, et al. Agonist-independent modulation of N-type calcium channels by ORL1 receptors. Nat Neurosci 2004; 7: 118-25.
-
(2004)
Nat Neurosci
, vol.7
, pp. 118-125
-
-
Beedle, A.M.1
McRory, J.E.2
Poirot, O.3
-
30
-
-
10944242312
-
2+ channel enhanced morphine analgesia and reduced morphine tolerance
-
2+ channel enhanced morphine analgesia and reduced morphine tolerance. Eur J Neurosci 2004; 20: 3516-9.
-
(2004)
Eur J Neurosci
, vol.20
, pp. 3516-3519
-
-
Yokoyama, K.1
Kurihara, T.2
Saegusa, H.3
-
33
-
-
0037174988
-
Pain perception in mice lacking the beta3 subunit of voltage-activated calcium channels
-
Murakami M, Fleischmann B, De Felipe C, et al. Pain perception in mice lacking the beta3 subunit of voltage-activated calcium channels. J Biol Chem 2002; 277: 40342-51.
-
(2002)
J Biol Chem
, vol.277
, pp. 40342-40351
-
-
Murakami, M.1
Fleischmann, B.2
De Felipe, C.3
-
34
-
-
0034068137
-
2+ channel alphal subunit contains an endoplasmic reticulum retention signal antagonized by the beta subunit
-
2+ channel alphal subunit contains an endoplasmic reticulum retention signal antagonized by the beta subunit. Neuron 2000; 25: 177-90.
-
(2000)
Neuron
, vol.25
, pp. 177-190
-
-
Bichet, D.1
Cornet, V.2
Geib, S.3
-
35
-
-
0242606215
-
Inhibition of voltage-gated calcium channels by sequestration of beta subunits
-
Cuchillo-Ibanez I, Aldea M, Brocard J, et al. Inhibition of voltage-gated calcium channels by sequestration of beta subunits. Biochem Biophys Res Commun 2003; 311: 1000-7.
-
(2003)
Biochem Biophys Res Commun
, vol.311
, pp. 1000-1007
-
-
Cuchillo-Ibanez, I.1
Aldea, M.2
Brocard, J.3
-
36
-
-
0035500748
-
Dorsal root ganglion neurons show increased expression of the calcium channel alpha2delta-l subunit following partial sciatic nerve injury
-
Newton RA, Bingham S, Case PC, et al. Dorsal root ganglion neurons show increased expression of the calcium channel alpha2delta-l subunit following partial sciatic nerve injury. Brain Res Mol Brain Res 2001; 95: 1-8.
-
(2001)
Brain Res Mol Brain Res
, vol.95
, pp. 1-8
-
-
Newton, R.A.1
Bingham, S.2
Case, P.C.3
-
37
-
-
0035869568
-
Upregulation of dorsal root ganglion (alpha)2(delta) calcium channel subunit and its correlation with allodynia in spinal nerve-injured rats
-
Luo ZD, Chaplan SR, Higuera ES, et al. Upregulation of dorsal root ganglion (alpha)2(delta) calcium channel subunit and its correlation with allodynia in spinal nerve-injured rats. J Neurosci 2001; 21: 1868-75.
-
(2001)
J Neurosci
, vol.21
, pp. 1868-1875
-
-
Luo, Z.D.1
Chaplan, S.R.2
Higuera, E.S.3
-
38
-
-
4744345338
-
Spinal dorsal horn calcium channel alpha2delta-1 subunit upregulation contributes to peripheral nerve injury-induced tactile allodynia
-
Li Cy, Song YH, Higuera ES, Luo ZD. Spinal dorsal horn calcium channel alpha2delta-1 subunit upregulation contributes to peripheral nerve injury-induced tactile allodynia. J Neurosci 2004; 24: 8494-9.
-
(2004)
J Neurosci
, vol.24
, pp. 8494-8499
-
-
Cy, L.1
Song, Y.H.2
Higuera, E.S.3
Luo, Z.D.4
-
39
-
-
0037019860
-
Mechanical and thermal antinociception in rats following systemic administration of mibefradil, a T-type calcium channel blocker
-
Todorovic SM, Meyenburg A, Jevtovic-Todorovic V. Mechanical and thermal antinociception in rats following systemic administration of mibefradil, a T-type calcium channel blocker. Brain Ses 2002; 951: 336-40.
-
(2002)
Brain Ses
, vol.951
, pp. 336-340
-
-
Todorovic, S.M.1
Meyenburg, A.2
Jevtovic-Todorovic, V.3
-
40
-
-
0141850350
-
Reversal of experimental neuropathic pain by T-type calcium channel blockers
-
Dogrul A, Gardell LR, Ossipov MH, et al. Reversal of experimental neuropathic pain by T-type calcium channel blockers. Pain 2005; 105: 159-68.
-
(2005)
Pain
, vol.105
, pp. 159-168
-
-
Dogrul, A.1
Gardell, L.R.2
Ossipov, M.H.3
-
41
-
-
1842786064
-
Ethosuximide reverses paclitaxel- and vincristine-induced painful peripheral neuropathy
-
Flatters SJ, Bennett GJ. Ethosuximide reverses paclitaxel- and vincristine-induced painful peripheral neuropathy. Pain 2004; 109: 150-61.
-
(2004)
Pain
, vol.109
, pp. 150-161
-
-
Flatters, S.J.1
Bennett, G.J.2
-
42
-
-
6944255279
-
2+ channels in rat sensory neurons in vitro and potent peripheral analgesics in vivo
-
2+ channels in rat sensory neurons in vitro and potent peripheral analgesics in vivo. Mol Pharmacol 2004; 66: 1223-35.
-
(2004)
Mol Pharmacol
, vol.66
, pp. 1223-1235
-
-
Todorovic, S.M.1
Pathirathna, S.2
Brimelow, B.C.3
-
44
-
-
20144385871
-
Silencing of the Ca(v)3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception
-
Bourinet E, Alloui A, Monteil A, et al. Silencing of the Ca(v)3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception. EMBO J 2005; 24: 315-24.
-
(2005)
EMBO J
, vol.24
, pp. 315-324
-
-
Bourinet, E.1
Alloui, A.2
Monteil, A.3
-
45
-
-
21344458578
-
COX-dependent mechanisms involved in the antinociceptive action of NSAIDs at central and peripheral sites
-
Burian M, Geisslinger G. COX-dependent mechanisms involved in the antinociceptive action of NSAIDs at central and peripheral sites. Pharmacol Ther 2005; 107: 139-54.
-
(2005)
Pharmacol Ther
, vol.107
, pp. 139-154
-
-
Burian, M.1
Geisslinger, G.2
-
46
-
-
23844432593
-
Mechanism-based treatment in chronic neuropathic pain: The role of antidepressants
-
Coluzzi F, Mattia C. Mechanism-based treatment in chronic neuropathic pain: the role of antidepressants. Curr Pharm Des 2005; 11: 2945-60.
-
(2005)
Curr Pharm Des
, vol.11
, pp. 2945-2960
-
-
Coluzzi, F.1
Mattia, C.2
-
47
-
-
0032769919
-
Ions in the fire: Recent ion-channel research and approaches to pain therapy
-
Eglen RM, Hunter JC, Dray A. Ions in the fire: recent ion-channel research and approaches to pain therapy. Trends Pharmacol Sci 1999; 20: 337-42.
-
(1999)
Trends Pharmacol Sci
, vol.20
, pp. 337-342
-
-
Eglen, R.M.1
Hunter, J.C.2
Dray, A.3
-
48
-
-
0037168683
-
A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat
-
Jarvis MF, Burgard EC, McGaraughty S, et al. A-317491, a novel potent and selective non-nucleotide antagonist of P2X3 and P2X2/3 receptors, reduces chronic inflammatory and neuropathic pain in the rat. Proc Natl Acad Sci USA 2002; 99: 17179-84.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 17179-17184
-
-
Jarvis, M.F.1
Burgard, E.C.2
McGaraughty, S.3
-
49
-
-
2642623583
-
Inflammatory mediators at acidic pH activate capsaicin receptors in cultured sensory neurons from newborn rats
-
Vyklicky L, Knotkova-Urbancova H, Vitaskova Z, et al. Inflammatory mediators at acidic pH activate capsaicin receptors in cultured sensory neurons from newborn rats. J Neurophysiol 1998; 79: 670-6.
-
(1998)
J Neurophysiol
, vol.79
, pp. 670-676
-
-
Vyklicky, L.1
Knotkova-Urbancova, H.2
Vitaskova, Z.3
-
50
-
-
2942575801
-
Acid-sensing ion channels (ASICs): New targets for the analgesic effects of non-steroid anti-inflammatory drugs (NSAIDs)
-
Voilley N. Acid-sensing ion channels (ASICs): new targets for the analgesic effects of non-steroid anti-inflammatory drugs (NSAIDs). Curr Drug Targets Inflamm Allergy 2004; 3: 71-9.
-
(2004)
Curr Drug Targets Inflamm Allergy
, vol.3
, pp. 71-79
-
-
Voilley, N.1
-
51
-
-
25644454237
-
NMDA receptor antagonist treatment at the time of nerve injury prevents injury-induced changes in spinal NR1 and NR2B subunit expression and increases the sensitivity of residual pain behaviours to subsequently administered NMDA receptor antagonists
-
Wilson JA, Garry EM, Anderson HA, et al. NMDA receptor antagonist treatment at the time of nerve injury prevents injury-induced changes in spinal NR1 and NR2B subunit expression and increases the sensitivity of residual pain behaviours to subsequently administered NMDA receptor antagonists. Pain 2005; 117: 421-32.
-
(2005)
Pain
, vol.117
, pp. 421-432
-
-
Wilson, J.A.1
Garry, E.M.2
Anderson, H.A.3
|