567 related articles for article (PubMed ID: 10620286)
1. Isoform-specific lidocaine block of sodium channels explained by differences in gating.
Nuss HB; Kambouris NG; Marbán E; Tomaselli GF; Balser JR
Biophys J; 2000 Jan; 78(1):200-10. PubMed ID: 10620286
[TBL] [Abstract][Full Text] [Related]
2. Cardiac sodium channels (hH1) are intrinsically more sensitive to block by lidocaine than are skeletal muscle (mu 1) channels.
Nuss HB; Tomaselli GF; Marbán E
J Gen Physiol; 1995 Dec; 106(6):1193-209. PubMed ID: 8786356
[TBL] [Abstract][Full Text] [Related]
3. Functional consequences of lidocaine binding to slow-inactivated sodium channels.
Balser JR; Nuss HB; Romashko DN; Marban E; Tomaselli GF
J Gen Physiol; 1996 May; 107(5):643-58. PubMed ID: 8740377
[TBL] [Abstract][Full Text] [Related]
4. Channel activation voltage alone is directly altered in an isoform-specific manner by Na(v1.4) and Na(v1.5) cytoplasmic linkers.
Bennett ES
J Membr Biol; 2004 Feb; 197(3):155-68. PubMed ID: 15042347
[TBL] [Abstract][Full Text] [Related]
5. Comparison of slow inactivation in human heart and rat skeletal muscle Na+ channel chimaeras.
O'Reilly JP; Wang SY; Kallen RG; Wang GK
J Physiol; 1999 Feb; 515 ( Pt 1)(Pt 1):61-73. PubMed ID: 9925878
[TBL] [Abstract][Full Text] [Related]
6. 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
J Gen Physiol; 2004 Dec; 124(6):691-701. PubMed ID: 15545401
[TBL] [Abstract][Full Text] [Related]
7. Characterization of the isoform-specific differences in the gating of neuronal and muscle sodium channels.
O'Leary ME
Can J Physiol Pharmacol; 1998; 76(10-11):1041-50. PubMed ID: 10100887
[TBL] [Abstract][Full Text] [Related]
8. Lidocaine induces a slow inactivated state in rat skeletal muscle sodium channels.
Chen Z; Ong BH; Kambouris NG; Marbán E; Tomaselli GF; Balser JR
J Physiol; 2000 Apr; 524 Pt 1(Pt 1):37-49. PubMed ID: 10747182
[TBL] [Abstract][Full Text] [Related]
9. Differences in steady-state inactivation between Na channel isoforms affect local anesthetic binding affinity.
Wright SN; Wang SY; Kallen RG; Wang GK
Biophys J; 1997 Aug; 73(2):779-88. PubMed ID: 9251794
[TBL] [Abstract][Full Text] [Related]
10. A critical residue for isoform difference in tetrodotoxin affinity is a molecular determinant of the external access path for local anesthetics in the cardiac sodium channel.
Sunami A; Glaaser IW; Fozzard HA
Proc Natl Acad Sci U S A; 2000 Feb; 97(5):2326-31. PubMed ID: 10681444
[TBL] [Abstract][Full Text] [Related]
11. A comparative study of the action of tolperisone on seven different voltage dependent sodium channel isoforms.
Hofer D; Lohberger B; Steinecker B; Schmidt K; Quasthoff S; Schreibmayer W
Eur J Pharmacol; 2006 May; 538(1-3):5-14. PubMed ID: 16650844
[TBL] [Abstract][Full Text] [Related]
12. Dissecting lidocaine action: diethylamide and phenol mimic separate modes of lidocaine block of sodium channels from heart and skeletal muscle.
Zamponi GW; French RJ
Biophys J; 1993 Dec; 65(6):2335-47. PubMed ID: 8312473
[TBL] [Abstract][Full Text] [Related]
13. State-dependent cocaine block of sodium channel isoforms, chimeras, and channels coexpressed with the beta1 subunit.
Wright SN; Wang SY; Xiao YF; Wang GK
Biophys J; 1999 Jan; 76(1 Pt 1):233-45. PubMed ID: 9876137
[TBL] [Abstract][Full Text] [Related]
14. Sodium channel isoform-specific effects of halothane: protein kinase C co-expression and slow inactivation gating.
Patel MK; Mistry D; John JE; Mounsey JP
Br J Pharmacol; 2000 Aug; 130(8):1785-92. PubMed ID: 10952666
[TBL] [Abstract][Full Text] [Related]
15. Isoform-selective effects of isoflurane on voltage-gated Na+ channels.
OuYang W; Hemmings HC
Anesthesiology; 2007 Jul; 107(1):91-8. PubMed ID: 17585220
[TBL] [Abstract][Full Text] [Related]
16. Coexpression of beta 1 with cardiac sodium channel alpha subunits in oocytes decreases lidocaine block.
Makielski JC; Limberis JT; Chang SY; Fan Z; Kyle JW
Mol Pharmacol; 1996 Jan; 49(1):30-9. PubMed ID: 8569709
[TBL] [Abstract][Full Text] [Related]
17. Fast-onset lidocaine block of rat NaV1.4 channels suggests involvement of a second high-affinity open state.
Gingrich KJ; Wagner LE
Biochim Biophys Acta; 2016 Jun; 1858(6):1175-88. PubMed ID: 26922882
[TBL] [Abstract][Full Text] [Related]
18. Effect of lidocaine on the slow Na+ channels of Xenopus oocytes.
Charpentier G
Gen Physiol Biophys; 2002 Dec; 21(4):355-65. PubMed ID: 12693709
[TBL] [Abstract][Full Text] [Related]
19. An improved model for the binding of lidocaine and structurally related local anaesthetics to fast-inactivated voltage-operated sodium channels, showing evidence of cooperativity.
Leuwer M; Haeseler G; Hecker H; Bufler J; Dengler R; Aronson JK
Br J Pharmacol; 2004 Jan; 141(1):47-54. PubMed ID: 14662728
[TBL] [Abstract][Full Text] [Related]
20. Intrinsic lidocaine affinity for Na channels expressed in Xenopus oocytes depends on alpha (hH1 vs. rSkM1) and beta 1 subunits.
Makielski JC; Limberis J; Fan Z; Kyle JW
Cardiovasc Res; 1999 May; 42(2):503-9. PubMed ID: 10533585
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
