Sleeper A A, Cummins T R, Dib-Hajj S D, Hormuzdiar W, Tyrrell L, Waxman S G, Black J A
Department of Neurology and Paralyzed Veterans of America/Eastern Paralyzed Veterans Association Neuroscience Research Center, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Neurosci. 2000 Oct 1;20(19):7279-89. doi: 10.1523/JNEUROSCI.20-19-07279.2000.
Two TTX-resistant sodium channels, SNS and NaN, are preferentially expressed in c-type dorsal root ganglion (DRG) neurons and have been shown recently to have distinct electrophysiological signatures, SNS producing a slowly inactivating and NaN producing a persistent sodium current with a relatively hyperpolarized voltage-dependence. An attenuation of SNS and NaN transcripts has been demonstrated in small DRG neurons after transection of the sciatic nerve. However, it is not known whether changes in the currents associated with SNS and NaN or in the expression of SNS and NaN channel protein occur after axotomy of the peripheral projections of DRG neurons or whether similar changes occur after transection of the central (dorsal root) projections of DRG neurons. Peripheral and central projections of L4/5 DRG neurons in adult rats were axotomized by transection of the sciatic nerve and the L4 and L5 dorsal roots, respectively. DRG neurons were examined using immunocytochemical and patch-clamp methods 9-12 d after sciatic nerve or dorsal root lesion. Levels of SNS and NaN protein in the two types of injuries were paralleled by their respective TTX-resistant currents. There was a significant decrease in SNS and NaN signal intensity in small DRG neurons after peripheral, but not central, axotomy compared with control neurons. Likewise, there was a significant reduction in slowly inactivating and persistent TTX-resistant currents in these neurons after peripheral, but not central, axotomy compared with control neurons. These results indicate that peripheral, but not central, axotomy results in a reduction in expression of functional SNS and NaN channels in c-type DRG neurons and suggest a basis for the altered electrical properties that are observed after peripheral nerve injury.
两种对河豚毒素(TTX)不敏感的钠通道,即SNS和NaN,优先表达于c型背根神经节(DRG)神经元中,并且最近已显示出具有不同的电生理特征,SNS产生缓慢失活的电流,而NaN产生具有相对超极化电压依赖性的持续性钠电流。坐骨神经横断后,已证实在小DRG神经元中SNS和NaN转录本减少。然而,尚不清楚DRG神经元外周投射轴突切断后,与SNS和NaN相关的电流变化或SNS和NaN通道蛋白的表达是否会发生变化,也不清楚DRG神经元中枢(背根)投射横断后是否会发生类似变化。分别通过切断坐骨神经和L4、L5背根,对成年大鼠L4/5 DRG神经元的外周和中枢投射进行轴突切断。在坐骨神经或背根损伤后9 - 12天,使用免疫细胞化学和膜片钳方法检查DRG神经元。两种损伤类型中SNS和NaN蛋白水平与其各自的TTX不敏感电流平行。与对照神经元相比,外周轴突切断后小DRG神经元中SNS和NaN信号强度显著降低,但中枢轴突切断后未出现这种情况。同样,与对照神经元相比,外周轴突切断后这些神经元中缓慢失活和持续性TTX不敏感电流显著降低,但中枢轴突切断后未出现这种情况。这些结果表明,外周而非中枢轴突切断导致c型DRG神经元中功能性SNS和NaN通道表达减少,并为外周神经损伤后观察到的电特性改变提供了一个基础。