-
1
-
-
0030580280
-
Multiple opioid receptor-like genes are identified in diverse vertebrate phyla
-
Li X, Keith DE Jr, Evans CJ: Multiple opioid receptor-like genes are identified in diverse vertebrate phyla. FEBS Lett 1996; 397:25-9
-
(1996)
FEBS Lett
, vol.397
, pp. 25-29
-
-
Li, X.1
Keith Jr., D.E.2
Evans, C.J.3
-
2
-
-
0033825829
-
Opioid receptors: From genes to mice
-
Kieffer BL: Opioid receptors: From genes to mice. J Pain 2000; 1:45-50
-
(2000)
J Pain
, vol.1
, pp. 45-50
-
-
Kieffer, B.L.1
-
3
-
-
0029852678
-
Loss of morphineinduced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene
-
Matthes HW, Maldonado R, Simonin F, Valverde O, Slowe S, Kitchen I, Befort K, Dierich A, Le Meur M, Dollé P, Tzavara E, Hanoune J, Roques BP, Kieffer BL: Loss of morphineinduced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene. Nature 1996; 383:819-23
-
(1996)
Nature
, vol.383
, pp. 819-823
-
-
Matthes, H.W.1
Maldonado, R.2
Simonin, F.3
Valverde, O.4
Slowe, S.5
Kitchen, I.6
Befort, K.7
Dierich, A.8
Le Meur, M.9
Dollé, P.10
Tzavara, E.11
Hanoune, J.12
Roques, B.P.13
Kieffer, B.L.14
-
4
-
-
0031030042
-
Opiate receptor knockout mice define mu receptor roles in endogenous nociceptive responses and morphine-induced analgesia
-
Sora I, Takahashi N, Funada M, Ujike H, Revay RS, Donovan DM, Miner LL, Uhl GR: Opiate receptor knockout mice define mu receptor roles in endogenous nociceptive responses and morphine-induced analgesia. Proc Natl Acad Sci USA 1997; 94:1544-9
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 1544-1549
-
-
Sora, I.1
Takahashi, N.2
Funada, M.3
Ujike, H.4
Revay, R.S.5
Donovan, D.M.6
Miner, L.L.7
Uhl, G.R.8
-
5
-
-
0033013383
-
Opioids: First lessons from knockout mice
-
Kieffer BL: Opioids: First lessons from knockout mice. Trends Pharmacol Sci 1999; 20:19-26
-
(1999)
Trends Pharmacol Sci
, vol.20
, pp. 19-26
-
-
Kieffer, B.L.1
-
6
-
-
0036551766
-
Opioid receptor genes inactivated in mice: The highlights
-
Gavériaux-Ruff C, Kieffer BL: Opioid receptor genes inactivated in mice: The highlights. Neuropeptides 2002; 36: 62-71
-
(2002)
Neuropeptides
, vol.36
, pp. 62-71
-
-
Gavériaux-Ruff, C.1
Kieffer, B.L.2
-
7
-
-
0028385286
-
μ-Opioid agonists inhibit spinal trigeminal substantia gelatinosa neurons in guinea pig and rat
-
Grudt TJ, Williams JT:μ-Opioid agonists inhibit spinal trigeminal substantia gelatinosa neurons in guinea pig and rat. J Neurosci 1994; 14:1646-54
-
(1994)
J Neurosci
, vol.14
, pp. 1646-1654
-
-
Grudt, T.J.1
Williams, J.T.2
-
8
-
-
0033178720
-
Actions of opioids on excitatory and inhibitory transmission in substantia gelatinosa of adult rat spinal cord
-
Kohno T, Kumamoto E, Higashi H, Shimoji K, Yoshimura M: Actions of opioids on excitatory and inhibitory transmission in substantia gelatinosa of adult rat spinal cord. J Physiol 1999; 518(Pt 3):803-13
-
(1999)
J Physiol
, vol.518
, Issue.PART 3
, pp. 803-813
-
-
Kohno, T.1
Kumamoto, E.2
Higashi, H.3
Shimoji, K.4
Yoshimura, M.5
-
9
-
-
33947602618
-
The impact of opioid-induced hyperalgesia for postoperative pain
-
Koppert W, Schmelz M: The impact of opioid-induced hyperalgesia for postoperative pain. Best Pract Res Clin Anaesthesiol 2007; 21:65-83
-
(2007)
Best Pract Res Clin Anaesthesiol
, vol.21
, pp. 65-83
-
-
Koppert, W.1
Schmelz, M.2
-
10
-
-
0037454943
-
Opioid-induced hyperalgesia: Abnormal or normal pain?
-
Simonnet G, Rivat C: Opioid-induced hyperalgesia: Abnormal or normal pain? Neuroreport 2003; 14:1-7
-
(2003)
Neuroreport
, vol.14
, pp. 1-7
-
-
Simonnet, G.1
Rivat, C.2
-
11
-
-
27644454229
-
Different profiles of buprenorphineinduced analgesia and antihyperalgesia in a human pain model
-
Koppert W, Ihmsen H, Körber N, Wehrfritz A, Sittl R, Schmelz M, Schüttler J: Different profiles of buprenorphineinduced analgesia and antihyperalgesia in a human pain model. Pain 2005; 118:15-22
-
(2005)
Pain
, vol.118
, pp. 15-22
-
-
Koppert, W.1
Ihmsen, H.2
Körber, N.3
Wehrfritz, A.4
Sittl, R.5
Schmelz, M.6
Schüttler, J.7
-
12
-
-
4644245300
-
Buprenorphine: A unique drug with complex pharmacology
-
Lutfy K, Cowan A: Buprenorphine: A unique drug with complex pharmacology. Curr Neuropharmacol 2004; 2:395-402
-
(2004)
Curr Neuropharmacol
, vol.2
, pp. 395-402
-
-
Lutfy, K.1
Cowan, A.2
-
13
-
-
60649101560
-
Clinical update on the pharmacology, efficacy and safety of transdermal buprenorphine
-
Kress HG: Clinical update on the pharmacology, efficacy and safety of transdermal buprenorphine. Eur J Pain 2009; 13: 219-30
-
(2009)
Eur J Pain
, vol.13
, pp. 219-230
-
-
Kress, H.G.1
-
14
-
-
0345687444
-
Buprenorphine-induced antinociception is mediated by mu-opioid receptors and compromised by concomitant activation of opioid receptor-like receptors
-
Lutfy K, Eitan S, Bryant CD, Yang YC, Saliminejad N, Walwyn W, Kieffer BL, Takeshima H, Carroll FI, Maidment NT, Evans CJ: Buprenorphine-induced antinociception is mediated by mu-opioid receptors and compromised by concomitant activation of opioid receptor-like receptors. J Neurosci 2003; 23:10331-7
-
(2003)
J Neurosci
, vol.23
, pp. 10331-10337
-
-
Lutfy, K.1
Eitan, S.2
Bryant, C.D.3
Yang, Y.C.4
Saliminejad, N.5
Walwyn, W.6
Kieffer, B.L.7
Takeshima, H.8
Carroll, F.I.9
Maidment, N.T.10
Evans, C.J.11
-
15
-
-
0034666274
-
Dynorphin promotes abnormal pain and spinal opioid antinociceptive tolerance
-
Vanderah TW, Gardell LR, Burgess SE, Ibrahim M, Dogrul A, Zhong CM, Zhang ET, Malan TP Jr, Ossipov MH, Lai J, Porreca F: Dynorphin promotes abnormal pain and spinal opioid antinociceptive tolerance. J Neurosci 2000; 20: 7074-9
-
(2000)
J Neurosci
, vol.20
, pp. 7074-7079
-
-
Vanderah, T.W.1
Gardell, L.R.2
Burgess, S.E.3
Ibrahim, M.4
Dogrul, A.5
Zhong, C.M.6
Zhang, E.T.7
Malan Jr., T.P.8
Ossipov, M.H.9
Lai, J.10
Porreca, F.11
-
16
-
-
0024992881
-
Intrathecal etorphine, fentanyl and buprenorphine on spinal nociceptive neurones in the rat
-
Dickenson AH, Sullivan AF, McQuay HJ: Intrathecal etorphine, fentanyl and buprenorphine on spinal nociceptive neurones in the rat. Pain 1990; 42:227-34
-
(1990)
Pain
, vol.42
, pp. 227-234
-
-
Dickenson, A.H.1
Sullivan, A.F.2
McQuay, H.J.3
-
17
-
-
0032923766
-
Intra-articular buprenorphine after knee arthroscopy. A randomised, prospective, double-blind study
-
Varrassi G, Marinangeli F, Ciccozzi A, Iovinelli G, Facchetti G, Ciccone A: Intra-articular buprenorphine after knee arthroscopy. A randomised, prospective, double-blind study. Acta Anaesthesiol Scand 1999; 43:51-5
-
(1999)
Acta Anaesthesiol Scand
, vol.43
, pp. 51-55
-
-
Varrassi, G.1
Marinangeli, F.2
Ciccozzi, A.3
Iovinelli, G.4
Facchetti, G.5
Ciccone, A.6
-
19
-
-
0034895045
-
A new model of electrically evoked pain and hyperalgesia in human skin: The effects of intravenous alfentanil, S(+)-ketamine, and lidocaine
-
Koppert W, Dern SK, Sittl R, Albrecht S, Schüttler J, Schmelz M: A new model of electrically evoked pain and hyperalgesia in human skin: The effects of intravenous alfentanil, S(+)-ketamine, and lidocaine. ANESTHESIOLOGY 2001; 95:395-402
-
(2001)
Anesthesiology
, vol.95
, pp. 395-402
-
-
Koppert, W.1
Dern, S.K.2
Sittl, R.3
Albrecht, S.4
Schüttler, J.5
Schmelz, M.6
-
20
-
-
11244253209
-
Interactions of local anesthetics with voltage-gated Na+channels
-
Nau C, Wang GK: Interactions of local anesthetics with voltage-gated Na+channels. J Membr Biol 2004; 201:1-8
-
(2004)
J Membr Biol
, vol.201
, pp. 1-8
-
-
Nau, C.1
Wang, G.K.2
-
21
-
-
77649187664
-
Block of sensory neuronal Na+channels by the secreolytic ambroxol is associated with an interaction with local anesthetic binding sites
-
Leffler A, Reckzeh J, Nau C: Block of sensory neuronal Na+channels by the secreolytic ambroxol is associated with an interaction with local anesthetic binding sites. Eur J Pharmacol 2010; 630:19-28
-
(2010)
Eur J Pharmacol
, vol.630
, pp. 19-28
-
-
Leffler, A.1
Reckzeh, J.2
Nau, C.3
-
22
-
-
33845872615
-
Use-dependent block by lidocaine but not amitriptyline is more pronounced in tetrodotoxin (TTX)-Resistant Nav1.8 than in TTX-sensitive Na+channels
-
Leffler A, Reiprich A, Mohapatra DP, Nau C: Use-dependent block by lidocaine but not amitriptyline is more pronounced in tetrodotoxin (TTX)-Resistant Nav1.8 than in TTX-sensitive Na+channels. J Pharmacol Exp Ther 2007; 320:354-64
-
(2007)
J Pharmacol Exp Ther
, vol.320
, pp. 354-364
-
-
Leffler, A.1
Reiprich, A.2
Mohapatra, D.P.3
Nau, C.4
-
23
-
-
0022903329
-
Sensory receptors in mammalian skin in an in vitro preparation
-
Reeh PW: Sensory receptors in mammalian skin in an in vitro preparation. Neurosci Lett 1986; 66:141-6
-
(1986)
Neurosci Lett
, vol.66
, pp. 141-146
-
-
Reeh, P.W.1
-
24
-
-
59849121339
-
Phenotyping sensory nerve endings in vitro in the mouse
-
Zimmermann K, Hein A, Hager U, Kaczmarek JS, Turnquist BP, Clapham DE, Reeh PW: Phenotyping sensory nerve endings in vitro in the mouse. Nat Protoc 2009; 4:174-96
-
(2009)
Nat Protoc
, vol.4
, pp. 174-196
-
-
Zimmermann, K.1
Hein, A.2
Hager, U.3
Kaczmarek, J.S.4
Turnquist, B.P.5
Clapham, D.E.6
Reeh, P.W.7
-
25
-
-
0038102242
-
Point mutations at L1280 in Nav1.4 channel D3-S6 modulate binding affinity and stereoselectivity of bupivacaine enantiomers
-
Nau C, Wang SY, Wang GK: Point mutations at L1280 in Nav1.4 channel D3-S6 modulate binding affinity and stereoselectivity of bupivacaine enantiomers. Mol Pharmacol 2003; 63:1398-406
-
(2003)
Mol Pharmacol
, vol.63
, pp. 1398-1406
-
-
Nau, C.1
Wang, S.Y.2
Wang, G.K.3
-
26
-
-
0032794137
-
Point mutations at N434 in D1-S6 of mu1 Na(+) channels modulate binding affinity and stereoselectivity of local anesthetic enantiomers
-
Nau C, Wang SY, Strichartz GR, Wang GK: Point mutations at N434 in D1-S6 of mu1 Na(+) channels modulate binding affinity and stereoselectivity of local anesthetic enantiomers. Mol Pharmacol 1999; 56:404-13
-
(1999)
Mol Pharmacol
, vol.56
, pp. 404-413
-
-
Nau, C.1
Wang, S.Y.2
Strichartz, G.R.3
Wang, G.K.4
-
28
-
-
70149112082
-
Using lidocaine and benzocaine to link sodium channel molecular conformations to state-dependent antiarrhythmic drug affinity
-
Hanck DA, Nikitina E, McNulty MM, Fozzard HA, Lipkind GM, Sheets MF: Using lidocaine and benzocaine to link sodium channel molecular conformations to state-dependent antiarrhythmic drug affinity. Circ Res 2009; 105:492-9
-
(2009)
Circ Res
, vol.105
, pp. 492-499
-
-
Hanck, D.A.1
Nikitina, E.2
McNulty, M.M.3
Fozzard, H.A.4
Lipkind, G.M.5
Sheets, M.F.6
-
29
-
-
1242341914
-
Mexiletine block of wild-type and inactivation-deficient human skeletal muscle hNav1.4 Na+channels
-
Wang GK, Russell C, Wang SY: Mexiletine block of wild-type and inactivation-deficient human skeletal muscle hNav1.4 Na+channels. J Physiol 2004; 554:621-33
-
(2004)
J Physiol
, vol.554
, pp. 621-633
-
-
Wang, G.K.1
Russell, C.2
Wang, S.Y.3
-
30
-
-
0141848333
-
State-dependent block of wild-type and inactivation-deficient Na+channels by flecainide
-
Wang GK, Russell C, Wang SY: State-dependent block of wild-type and inactivation-deficient Na+channels by flecainide. J Gen Physiol 2003; 122:365-74
-
(2003)
J Gen Physiol
, vol.122
, pp. 365-374
-
-
Wang, G.K.1
Russell, C.2
Wang, S.Y.3
-
32
-
-
33750967055
-
Tramadol, fentanyl and sufentanil but not morphine block voltage-operated sodium channels
-
Haeseler G, Foadi N, Ahrens J, Dengler R, Hecker H, Leuwer M: Tramadol, fentanyl and sufentanil but not morphine block voltage-operated sodium channels. Pain 2006; 126:234-44
-
(2006)
Pain
, vol.126
, pp. 234-244
-
-
Haeseler, G.1
Foadi, N.2
Ahrens, J.3
Dengler, R.4
Hecker, H.5
Leuwer, M.6
-
33
-
-
0032722281
-
Meperidine and lidocaine block of recombinant voltage-dependent Na+channels: Evidence that meperidine is a local anesthetic
-
Wagner LE 2nd, Eaton M, Sabnis SS, Gingrich KJ: Meperidine and lidocaine block of recombinant voltage-dependent Na+channels: Evidence that meperidine is a local anesthetic. ANESTHESIOLOGY 1999; 91:1481-90
-
(1999)
Anesthesiology
, vol.91
, pp. 1481-1490
-
-
Wagner, I.I.L.E.1
Eaton, M.2
Sabnis, S.S.3
Gingrich, K.J.4
-
34
-
-
0036097888
-
Sodium channel blocking actions of the kappa-opioid receptor agonist U50, 488 contribute to its visceral antinociceptive effects
-
Su X, Joshi SK, Kardos S, Gebhart GF: Sodium channel blocking actions of the kappa-opioid receptor agonist U50, 488 contribute to its visceral antinociceptive effects. J Neurophysiol 2002; 87:1271-9
-
(2002)
J Neurophysiol
, vol.87
, pp. 1271-1279
-
-
Su, X.1
Joshi, S.K.2
Kardos, S.3
Gebhart, G.F.4
-
36
-
-
0018147760
-
Human pharmacology and abuse potential of the analgesic buprenorphine: A potential agent for treating narcotic addiction
-
Jasinski DR, Pevnick JS, Griffith JD: Human pharmacology and abuse potential of the analgesic buprenorphine: A potential agent for treating narcotic addiction. Arch Gen Psychiatry 1978; 35:501-16
-
(1978)
Arch Gen Psychiatry
, vol.35
, pp. 501-516
-
-
Jasinski, D.R.1
Pevnick, J.S.2
Griffith, J.D.3
-
37
-
-
77950953931
-
The tetrodotoxin-resistant Na+channel Na (v)1.8 reduces the potency of local anesthetics in blocking C-fiber nociceptors
-
Kistner K, Zimmermann K, Ehnert C, Reeh PW, Leffler A: The tetrodotoxin-resistant Na+channel Na (v)1.8 reduces the potency of local anesthetics in blocking C-fiber nociceptors. Pflugers Arch 2010; 459:751-63
-
(2010)
Pflugers Arch
, vol.459
, pp. 751-763
-
-
Kistner, K.1
Zimmermann, K.2
Ehnert, C.3
Reeh, P.W.4
Leffler, A.5
-
38
-
-
0025334884
-
Dose-response inhibition of rat compound nerve action potential by dextropropoxyphene and codeine compared to morphine and cocaine in vitro
-
Brodin P, Skoglund LA: Dose-response inhibition of rat compound nerve action potential by dextropropoxyphene and codeine compared to morphine and cocaine in vitro. Gen Pharmacol 1990; 21:551-3
-
(1990)
Gen Pharmacol
, vol.21
, pp. 551-553
-
-
Brodin, P.1
Skoglund, L.A.2
-
39
-
-
47549094820
-
Inhibitory effects of opioids on compound action potentials in frog sciatic nerves and their chemical structures
-
Mizuta K, Fujita T, Nakatsuka T, Kumamoto E: Inhibitory effects of opioids on compound action potentials in frog sciatic nerves and their chemical structures. Life Sci 2008; 83:198-207
-
(2008)
Life Sci
, vol.83
, pp. 198-207
-
-
Mizuta, K.1
Fujita, T.2
Nakatsuka, T.3
Kumamoto, E.4
-
40
-
-
14544277512
-
Transdermal buprenorphine for treating nociceptive and neuropathic pain: Four case studies
-
Likar R, Sittl R: Transdermal buprenorphine for treating nociceptive and neuropathic pain: Four case studies. Anesth Analg 2005; 100:781-5
-
(2005)
Anesth Analg
, vol.100
, pp. 781-785
-
-
Likar, R.1
Sittl, R.2
-
41
-
-
0031938853
-
Dose-response relationship of opioids in nociceptive and neuropathic postoperative pain
-
Benedetti F, Vighetti S, Amanzio M, Casadio C, Oliaro A, Bergamasco B, Maggi G: Dose-response relationship of opioids in nociceptive and neuropathic postoperative pain. Pain 1998; 74:205-11
-
(1998)
Pain
, vol.74
, pp. 205-211
-
-
Benedetti, F.1
Vighetti, S.2
Amanzio, M.3
Casadio, C.4
Oliaro, A.5
Bergamasco, B.6
Maggi, G.7
-
42
-
-
43549096159
-
Supra-additive effects of tramadol and acetaminophen in a human pain model
-
Filitz J, Ihmsen H, Günther W, Tröster A, Schwilden H, Schüttler J, Koppert W: Supra-additive effects of tramadol and acetaminophen in a human pain model. Pain 2008; 136:262-70
-
(2008)
Pain
, vol.136
, pp. 262-270
-
-
Filitz, J.1
Ihmsen, H.2
Günther, W.3
Tröster, A.4
Schwilden, H.5
Schüttler, J.6
Koppert, W.7
-
43
-
-
0142196082
-
Shortterm infusion of the mu-opioid agonist remifentanil in humans causes hyperalgesia during withdrawal
-
Angst MS, Koppert W, Pahl I, Clark DJ, Schmelz M: Shortterm infusion of the mu-opioid agonist remifentanil in humans causes hyperalgesia during withdrawal. Pain 2003; 106:49-57
-
(2003)
Pain
, vol.106
, pp. 49-57
-
-
Angst, M.S.1
Koppert, W.2
Pahl, I.3
Clark, D.J.4
Schmelz, M.5
-
44
-
-
0033963154
-
Low-dose lidocaine reduces secondary hyperalgesia by a central mode of action
-
Koppert W, Ostermeier N, Sittl R, Weidner C, Schmelz M: Low-dose lidocaine reduces secondary hyperalgesia by a central mode of action. Pain 2000; 85:217-24
-
(2000)
Pain
, vol.85
, pp. 217-224
-
-
Koppert, W.1
Ostermeier, N.2
Sittl, R.3
Weidner, C.4
Schmelz, M.5
-
45
-
-
0032421304
-
Low-dose lidocaine suppresses experimentally induced hyperalgesia in humans
-
Koppert W, Zeck S, Sittl R, Likar R, Knoll R, Schmelz M: Low-dose lidocaine suppresses experimentally induced hyperalgesia in humans. ANESTHESIOLOGY 1998; 89:1345-53
-
(1998)
Anesthesiology
, vol.89
, pp. 1345-1353
-
-
Koppert, W.1
Zeck, S.2
Sittl, R.3
Likar, R.4
Knoll, R.5
Schmelz, M.6
-
46
-
-
10344264994
-
Block of inactivation-deficient Na+channels by local anesthetics in stably transfected mammalian cells: Evidence for drug binding along the activation pathway
-
Wang SY, Mitchell J, Moczydlowski E, Wang GK: Block of inactivation-deficient Na+channels by local anesthetics in stably transfected mammalian cells: Evidence for drug binding along the activation pathway. J Gen Physiol 2004; 124: 691-701
-
(2004)
J Gen Physiol
, vol.124
, pp. 691-701
-
-
Wang, S.Y.1
Mitchell, J.2
Moczydlowski, E.3
Wang, G.K.4
-
47
-
-
70349159150
-
Local anaesthetic adjuvants: Neuraxial versus peripheral nerve block
-
Axelsson K, Gupta A: Local anaesthetic adjuvants: Neuraxial versus peripheral nerve block. Curr Opin Anaesthesiol 2009; 22:649-54
-
(2009)
Curr Opin Anaesthesiol
, vol.22
, pp. 649-654
-
-
Axelsson, K.1
Gupta, A.2
|