116 related articles for article (PubMed ID: 8957220)
1. Vincamine and vincanol are potent blockers of voltage-gated Na+ channels.
Erdo SA; Molnár P; Lakics V; Bence JZ; Tömösközi Z
Eur J Pharmacol; 1996 Oct; 314(1-2):69-73. PubMed ID: 8957220
[TBL] [Abstract][Full Text] [Related]
2. Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons.
Molnár P; Erdö SL
Eur J Pharmacol; 1995 Feb; 273(3):303-6. PubMed ID: 7737339
[TBL] [Abstract][Full Text] [Related]
3. Protection against veratridine toxicity in rat cortical cultures: relationship to sodium channel blockade.
Lakics V; Molnár P; Erdö SL
Neuroreport; 1995 Dec; 7(1):89-92. PubMed ID: 8742424
[TBL] [Abstract][Full Text] [Related]
4. Vinpocetine is a highly potent neuroprotectant against veratridine-induced cell death in primary cultures of rat cerebral cortex.
Lakics V; Sebestyén MG; Erdö SL
Neurosci Lett; 1995 Feb; 185(2):127-30. PubMed ID: 7746503
[TBL] [Abstract][Full Text] [Related]
5. Effects of besipirdine at the voltage-dependent sodium channel.
Tang L; Smith CP; Huger FP; Kongsamut S
Br J Pharmacol; 1995 Nov; 116(5):2468-72. PubMed ID: 8581286
[TBL] [Abstract][Full Text] [Related]
6. BIIR 561 CL: a novel combined antagonist of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and voltage-dependent sodium channels with anticonvulsive and neuroprotective properties.
Weiser T; Brenner M; Palluk R; Bechtel WD; Ceci A; Brambilla A; Ensinger HA; Sagrada A; Wienrich M
J Pharmacol Exp Ther; 1999 Jun; 289(3):1343-9. PubMed ID: 10336525
[TBL] [Abstract][Full Text] [Related]
7. 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; 306(2):498-504. PubMed ID: 12730276
[TBL] [Abstract][Full Text] [Related]
8. Inhibition by propofol of [3H]-batrachotoxinin-A 20-alpha-benzoate binding to voltage-dependent sodium channels in rat cortical synaptosomes.
Ratnakumari L; Hemmings HC
Br J Pharmacol; 1996 Dec; 119(7):1498-504. PubMed ID: 8968561
[TBL] [Abstract][Full Text] [Related]
9. Single and combined effects of carbamazepine and vinpocetine on depolarization-induced changes in Na+, Ca2+ and glutamate release in hippocampal isolated nerve endings.
Sitges M; Chiu LM; Nekrassov V
Neurochem Int; 2006 Jul; 49(1):55-61. PubMed ID: 16621162
[TBL] [Abstract][Full Text] [Related]
10. A novel toxicity-based assay for the identification of modulators of voltage-gated Na+ channels.
Weiser T
J Neurosci Methods; 2004 Aug; 137(1):79-85. PubMed ID: 15196829
[TBL] [Abstract][Full Text] [Related]
11. The neuroprotective drug vinpocetine prevents veratridine-induced [Na+]i and [Ca2+]i rise in synaptosomes.
Tretter L; Adam-Vizi V
Neuroreport; 1998 Jun; 9(8):1849-53. PubMed ID: 9665614
[TBL] [Abstract][Full Text] [Related]
12. Vinpocetine selectively inhibits neurotransmitter release triggered by sodium channel activation.
Sitges M; Nekrassov V
Neurochem Res; 1999 Dec; 24(12):1585-91. PubMed ID: 10591410
[TBL] [Abstract][Full Text] [Related]
13. Voltage- and use-dependent inhibition of Na+ channels in rat sensory neurones by 4030W92, a new antihyperalgesic agent.
Trezise DJ; John VH; Xie XM
Br J Pharmacol; 1998 Jul; 124(5):953-63. PubMed ID: 9692781
[TBL] [Abstract][Full Text] [Related]
14. Inhibitory effects of vinpocetine on sodium current in rat cardiomyocytes.
Wei Y; Shi NC; Zhong CS; Zheng P; Liang ZJ
Zhongguo Yao Li Xue Bao; 1997 Sep; 18(5):411-5. PubMed ID: 10322929
[TBL] [Abstract][Full Text] [Related]
15. Neurotoxic action of veratridine in rat brain neuronal cultures: mechanism of neuroprotection by Ca++ antagonists nonselective for slow Ca++ channels.
Pauwels PJ; Van Assouw HP; Peeters L; Leysen JE
J Pharmacol Exp Ther; 1990 Dec; 255(3):1117-22. PubMed ID: 2175795
[TBL] [Abstract][Full Text] [Related]
16. Pharmacological characterization of Na+ influx via voltage-gated Na+ channels in spinal cord astrocytes.
Rose CR; Ransom BR; Waxman SG
J Neurophysiol; 1997 Dec; 78(6):3249-58. PubMed ID: 9405543
[TBL] [Abstract][Full Text] [Related]
17. Vinpocetine blockade of sodium channels inhibits the rise in sodium and calcium induced by 4-aminopyridine in synaptosomes.
Sitges M; Galván E; Nekrassov V
Neurochem Int; 2005 Jun; 46(7):533-40. PubMed ID: 15843047
[TBL] [Abstract][Full Text] [Related]
18. Sodium overload through voltage-dependent Na(+) channels induces necrosis and apoptosis of rat superior cervical ganglion cells in vitro.
Koike T; Tanaka S; Oda1 T; Ninomiya T
Brain Res Bull; 2000 Mar; 51(4):345-55. PubMed ID: 10704786
[TBL] [Abstract][Full Text] [Related]
19. Stereoselective modulatory actions of oleamide on GABA(A) receptors and voltage-gated Na(+) channels in vitro: a putative endogenous ligand for depressant drug sites in CNS.
Verdon B; Zheng J; Nicholson RA; Ganelli CR; Lees G
Br J Pharmacol; 2000 Jan; 129(2):283-90. PubMed ID: 10694234
[TBL] [Abstract][Full Text] [Related]
20. Comparative effects of ultra-short-acting beta1-blockers on voltage-gated tetrodotoxin-resistant Na+ channels in rat sensory neurons.
Tanahashi S; Iida H; Dohi S; Oda A; Osawa Y; Yamaguchi S
Eur J Anaesthesiol; 2009 Mar; 26(3):196-200. PubMed ID: 19237982
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
