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143 related items for PubMed ID: 19371587

  • 1. Functional and pharmacological properties of human and rat NaV1.8 channels.
    Browne LE, Clare JJ, Wray D.
    Neuropharmacology; 2009 Apr; 56(5):905-14. PubMed ID: 19371587
    [Abstract] [Full Text] [Related]

  • 2. Heterologous expression and functional analysis of rat Nav1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7-23.
    John VH, Main MJ, Powell AJ, Gladwell ZM, Hick C, Sidhu HS, Clare JJ, Tate S, Trezise DJ.
    Neuropharmacology; 2004 Mar; 46(3):425-38. PubMed ID: 14975698
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. V102862 (Co 102862): a potent, broad-spectrum state-dependent blocker of mammalian voltage-gated sodium channels.
    Ilyin VI, Hodges DD, Whittemore ER, Carter RB, Cai SX, Woodward RM.
    Br J Pharmacol; 2005 Mar; 144(6):801-12. PubMed ID: 15778702
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Effects of eugenol on Na+ currents in rat dorsal root ganglion neurons.
    Cho JS, Kim TH, Lim JM, Song JH.
    Brain Res; 2008 Dec 03; 1243():53-62. PubMed ID: 18824159
    [Abstract] [Full Text] [Related]

  • 8. Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
    Zhou X, Dong XW, Crona J, Maguire M, Priestley T.
    J Pharmacol Exp Ther; 2003 Aug 03; 306(2):498-504. PubMed ID: 12730276
    [Abstract] [Full Text] [Related]

  • 9. 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.
    Eur J Pharmacol; 2010 Mar 25; 630(1-3):19-28. PubMed ID: 20044988
    [Abstract] [Full Text] [Related]

  • 10. Inhibition of Nav1.7 and Nav1.4 sodium channels by trifluoperazine involves the local anesthetic receptor.
    Sheets PL, Gerner P, Wang CF, Wang SY, Wang GK, Cummins TR.
    J Neurophysiol; 2006 Oct 25; 96(4):1848-59. PubMed ID: 16807347
    [Abstract] [Full Text] [Related]

  • 11. The effect of kappa-opioid receptor agonists on tetrodotoxin-resistant sodium channels in primary sensory neurons.
    Su X, Castle NA, Antonio B, Roeloffs R, Thomas JB, Krafte DS, Chapman ML.
    Anesth Analg; 2009 Aug 25; 109(2):632-40. PubMed ID: 19608841
    [Abstract] [Full Text] [Related]

  • 12. Lysine point mutations in Na+ channel D4-S6 reduce inactivated channel block by local anesthetics.
    Wright SN, Wang SY, Wang GK.
    Mol Pharmacol; 1998 Oct 25; 54(4):733-9. PubMed ID: 9765517
    [Abstract] [Full Text] [Related]

  • 13. The anti-nociceptive agent ralfinamide inhibits tetrodotoxin-resistant and tetrodotoxin-sensitive Na+ currents in dorsal root ganglion neurons.
    Stummann TC, Salvati P, Fariello RG, Faravelli L.
    Eur J Pharmacol; 2005 Mar 14; 510(3):197-208. PubMed ID: 15763243
    [Abstract] [Full Text] [Related]

  • 14. Block of neuronal Na+ channels by antidepressant duloxetine in a state-dependent manner.
    Wang SY, Calderon J, Kuo Wang G.
    Anesthesiology; 2010 Sep 14; 113(3):655-65. PubMed ID: 20693878
    [Abstract] [Full Text] [Related]

  • 15. Effects of alpha2-adrenoceptor agonists on tetrodotoxin-resistant Na+ channels in rat dorsal root ganglion neurons.
    Oda A, Iida H, Tanahashi S, Osawa Y, Yamaguchi S, Dohi S.
    Eur J Anaesthesiol; 2007 Nov 14; 24(11):934-41. PubMed ID: 17568475
    [Abstract] [Full Text] [Related]

  • 16. Calmodulin regulates current density and frequency-dependent inhibition of sodium channel Nav1.8 in DRG neurons.
    Choi JS, Hudmon A, Waxman SG, Dib-Hajj SD.
    J Neurophysiol; 2006 Jul 14; 96(1):97-108. PubMed ID: 16598065
    [Abstract] [Full Text] [Related]

  • 17. High-affinity blockade of voltage-operated skeletal muscle sodium channels by 2,6-dimethyl-4-chlorophenol.
    Haeseler G, Gudehus S, Bufler J, Dengler R, Leuwer M.
    Eur J Anaesthesiol; 2006 Mar 14; 23(3):190-6. PubMed ID: 16430789
    [Abstract] [Full Text] [Related]

  • 18. Block of two subtypes of sodium channels in cockroach neurons by indoxacarb insecticides.
    Zhao X, Ikeda T, Salgado VL, Yeh JZ, Narahashi T.
    Neurotoxicology; 2005 Jun 14; 26(3):455-65. PubMed ID: 15935215
    [Abstract] [Full Text] [Related]

  • 19. Differential contribution of sodium channel subtypes to action potential generation in unmyelinated human C-type nerve fibers.
    Lang PM, Hilmer VB, Grafe P.
    Anesthesiology; 2007 Sep 14; 107(3):495-501. PubMed ID: 17721253
    [Abstract] [Full Text] [Related]

  • 20. Characterization of a new class of potent inhibitors of the voltage-gated sodium channel Nav1.7.
    Williams BS, Felix JP, Priest BT, Brochu RM, Dai K, Hoyt SB, London C, Tang YS, Duffy JL, Parsons WH, Kaczorowski GJ, Garcia ML.
    Biochemistry; 2007 Dec 18; 46(50):14693-703. PubMed ID: 18027973
    [Abstract] [Full Text] [Related]

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