Singh Jitendra N, Jain Gaurav, Ramarao Poduri, Sharma Shyam S
Electrophysiology Laboratory, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, S. A. S. Nagar (Mohali) - 160 062.
Indian J Physiol Pharmacol. 2009 Apr-Jun;53(2):147-54.
Carbamazepine (CBZ), one of the most commonly prescribed antiepileptic drug, is proposed to inhibit Na+ channel. In this study, we have investigated the effects of CBZ on Na+ current, evoked in cultured dorsal root ganglion (DRG) neurons from neonatal rats using whole cell patch clamp technique. In small DRG neurons (20-25 microm), Na+ current was obtained by blocking K+ and Ca2+ currents with appropriate ion replacement and channel blockers. Separation of the Na+ current components was achieved on the basis of response to the conditioning voltage. The CBZ depressed Na+ current in a dose-dependent manner. The maximal Na+ current was depressed at 300 microM of CBZ, where 94 +/- 5.1% of depression was observed. The depression of normalized current amplitude was found to be 72 +/- 13.2%, 84 +/- 10%, 85 +/- 7.1% and 95 +/- 5.2% at 10, 30, 100 and 300 microM of CBZ concentrations, respectively, at -20 mV test pulse, when compared with control. The depression of current amplitude was observed as 48 +/- 12.3%, 42 +/- 15.2%, 71 +/- 17.7% and 90 +/- 5.8% at 10, 30, 100 and 300 microM of CBZ concentration, respectively, at 0 mV voltage pulse. The depression of Na+ currents was found to be dose-dependant at -20 and -10 mV but not at 0 mV, It is concluded that the depression of Na+ currents by CBZ may be responsible for inhibiting the neurotransmitter release.
卡马西平(CBZ)是最常用的抗癫痫药物之一,其作用机制被认为是抑制钠离子通道。在本研究中,我们运用全细胞膜片钳技术,研究了卡马西平对新生大鼠培养背根神经节(DRG)神经元钠离子电流的影响。在小型DRG神经元(20 - 25微米)中,通过使用合适的离子替代物和通道阻滞剂阻断钾离子和钙离子电流来获得钠离子电流。基于对条件电压的反应实现了钠离子电流成分的分离。卡马西平以剂量依赖性方式抑制钠离子电流。在300微摩尔的卡马西平浓度下,最大钠离子电流受到抑制,观察到94±5.1%的抑制率。在 - 20毫伏测试脉冲下,与对照组相比,当卡马西平浓度分别为10、30、100和300微摩尔时,归一化电流幅度的抑制率分别为72±13.2%、84±10%、85±7.1%和95±5.2%。在0毫伏电压脉冲下,当卡马西平浓度分别为10、30、10