265 related articles for article (PubMed ID: 21232038)
1. Lidocaine reduces the transition to slow inactivation in Na(v)1.7 voltage-gated sodium channels.
Sheets PL; Jarecki BW; Cummins TR
Br J Pharmacol; 2011 Sep; 164(2b):719-30. PubMed ID: 21232038
[TBL] [Abstract][Full Text] [Related]
2. 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
Pflugers Arch; 2010 Apr; 459(5):751-63. PubMed ID: 20174994
[TBL] [Abstract][Full Text] [Related]
3. Differential block of sensory neuronal voltage-gated sodium channels by lacosamide [(2R)-2-(acetylamino)-N-benzyl-3-methoxypropanamide], lidocaine, and carbamazepine.
Sheets PL; Heers C; Stoehr T; Cummins TR
J Pharmacol Exp Ther; 2008 Jul; 326(1):89-99. PubMed ID: 18378801
[TBL] [Abstract][Full Text] [Related]
4. A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity.
Sheets PL; Jackson JO; Waxman SG; Dib-Hajj SD; Cummins TR
J Physiol; 2007 Jun; 581(Pt 3):1019-31. PubMed ID: 17430993
[TBL] [Abstract][Full Text] [Related]
5. Differential modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by the local anesthetic lidocaine.
Chevrier P; Vijayaragavan K; Chahine M
Br J Pharmacol; 2004 Jun; 142(3):576-84. PubMed ID: 15148257
[TBL] [Abstract][Full Text] [Related]
6. Functional tetrodotoxin-resistant Na(+) channels are expressed presynaptically in rat dorsal root ganglia neurons.
Medvedeva YV; Kim MS; Schnizler K; Usachev YM
Neuroscience; 2009 Mar; 159(2):559-69. PubMed ID: 19162133
[TBL] [Abstract][Full Text] [Related]
7. The position of the fast-inactivation gate during lidocaine block of voltage-gated Na+ channels.
Vedantham V; Cannon SC
J Gen Physiol; 1999 Jan; 113(1):7-16. PubMed ID: 9874684
[TBL] [Abstract][Full Text] [Related]
8. Outward stabilization of the S4 segments in domains III and IV enhances lidocaine block of sodium channels.
Sheets MF; Hanck DA
J Physiol; 2007 Jul; 582(Pt 1):317-34. PubMed ID: 17510181
[TBL] [Abstract][Full Text] [Related]
9. Local anesthetic-like inhibition of voltage-gated Na(+) channels by the partial μ-opioid receptor agonist buprenorphine.
Leffler A; Frank G; Kistner K; Niedermirtl F; Koppert W; Reeh PW; Nau C
Anesthesiology; 2012 Jun; 116(6):1335-46. PubMed ID: 22504149
[TBL] [Abstract][Full Text] [Related]
10. Paroxysmal extreme pain disorder mutations within the D3/S4-S5 linker of Nav1.7 cause moderate destabilization of fast inactivation.
Jarecki BW; Sheets PL; Jackson JO; Cummins TR
J Physiol; 2008 Sep; 586(17):4137-53. PubMed ID: 18599537
[TBL] [Abstract][Full Text] [Related]
11. Mechanisms of lidocaine's action on subtypes of spinal dorsal horn neurons subject to the diverse roles of Na(+) and K(+) channels in action potential generation.
Wolff M; Schnöbel-Ehehalt R; Mühling J; Weigand MA; Olschewski A
Anesth Analg; 2014 Aug; 119(2):463-470. PubMed ID: 24892804
[TBL] [Abstract][Full Text] [Related]
12. Lidocaine promotes the trafficking and functional expression of Na(v)1.8 sodium channels in mammalian cells.
Zhao J; Ziane R; Chatelier A; O'leary ME; Chahine M
J Neurophysiol; 2007 Jul; 98(1):467-77. PubMed ID: 17507497
[TBL] [Abstract][Full Text] [Related]
13. Block of tetrodotoxin-sensitive, Na(V)1.7 and tetrodotoxin-resistant, Na(V)1.8, Na+ channels by ranolazine.
Rajamani S; Shryock JC; Belardinelli L
Channels (Austin); 2008; 2(6):449-60. PubMed ID: 19077543
[TBL] [Abstract][Full Text] [Related]
14. 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
J Pharmacol Exp Ther; 2007 Jan; 320(1):354-64. PubMed ID: 17005919
[TBL] [Abstract][Full Text] [Related]
15. The opioid methadone induces a local anaesthetic-like inhibition of the cardiac Na⁺ channel, Na(v)1.5.
Schulze V; Stoetzer C; O'Reilly AO; Eberhardt E; Foadi N; Ahrens J; Wegner F; Lampert A; de la Roche J; Leffler A
Br J Pharmacol; 2014 Jan; 171(2):427-37. PubMed ID: 24117196
[TBL] [Abstract][Full Text] [Related]
16. Potent Inactivation-Dependent Inhibition of Adult and Neonatal NaV1.5 Channels by Lidocaine and Levobupivacaine.
Elajnaf T; Baptista-Hon DT; Hales TG
Anesth Analg; 2018 Sep; 127(3):650-660. PubMed ID: 29958221
[TBL] [Abstract][Full Text] [Related]
17. Two human paramyotonia congenita mutations have opposite effects on lidocaine block of Na+ channels expressed in a mammalian cell line.
Fan Z; George AL; Kyle JW; Makielski JC
J Physiol; 1996 Oct; 496 ( Pt 1)(Pt 1):275-86. PubMed ID: 8910215
[TBL] [Abstract][Full Text] [Related]
18. Mechanism of Modification, by Lidocaine, of Fast and Slow Recovery from Inactivation of Voltage-Gated Na⁺ Channels.
Gawali VS; Lukacs P; Cervenka R; Koenig X; Rubi L; Hilber K; Sandtner W; Todt H
Mol Pharmacol; 2015 Nov; 88(5):866-79. PubMed ID: 26358763
[TBL] [Abstract][Full Text] [Related]
19. Changes in the expression of tetrodotoxin-sensitive sodium channels within dorsal root ganglia neurons in inflammatory pain.
Black JA; Liu S; Tanaka M; Cummins TR; Waxman SG
Pain; 2004 Apr; 108(3):237-247. PubMed ID: 15030943
[TBL] [Abstract][Full Text] [Related]
20. Modulation of peripheral Na(+) channels and neuronal firing by n-butyl-p-aminobenzoate.
Thériault O; Poulin H; Sculptoreanu A; de Groat WC; O'Leary ME; Chahine M
Eur J Pharmacol; 2014 Mar; 727():158-66. PubMed ID: 24486399
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]