Sapunar Damir, Ljubkovic Marko, Lirk Philipp, McCallum J Bruce, Hogan Quinn H
Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
Anesthesiology. 2005 Aug;103(2):360-76. doi: 10.1097/00000542-200508000-00020.
Painful peripheral nerve injury results in disordered sensory neuron function that contributes to the pathogenesis of neuropathic pain. However, the relative roles of neurons with transected axons versus intact adjacent neurons have not been resolved. An essential first step is identification of electrophysiologic changes in these two neuronal populations after partial nerve damage.
Twenty days after spinal nerve ligation (SNL), intracellular recordings were obtained from axotomized fifth lumbar (L5) dorsal root ganglion neurons and adjacent, intact L4 neurons, as well as from control neurons and others subjected to sham-SNL surgery.
Pronounced electrophysiologic changes were seen only in L5 neurons after SNL. Both Aalpha/beta and Adelta neuron types showed increased action potential duration, decreased afterhyperpolarization amplitude and duration, and decreased current threshold for action potential initiation. Aalpha/beta neurons showed resting membrane potential depolarization, and increased repetitive firing during sustained depolarization developed in Adelta neurons. The afterhyperpolarization duration in neurons with C fibers shortened after axotomy. In contrast to the axotomized L5 neurons, neighboring L4 neurons showed no changes in action potential duration, afterhyperpolarization dimensions, or excitability after SNL. Depolarization rate (dV/dt) increased after SNL in L4 Aalpha/beta and Adelta neurons but decreased in L5 neurons. Time-dependent rectification during hyperpolarizing current injection (sag) was greater after SNL in Aalpha/beta L4 neurons compared with L5. Sham-SNL surgery produced only a decreased input resistance in Aalpha/beta neurons and a decreased conduction velocity in medium-sized cells. In the L5 ganglion after axotomy, a novel set of neurons, consisting of 24% of the myelinated population, exhibited long action potential durations despite myelinated neuron conduction velocities, particularly depolarized resting membrane potential, low depolarization rate, and absence of sag.
These findings indicate that nerve injury-induced electrical instability is restricted to axotomized neurons and is absent in adjacent intact neurons.
疼痛性周围神经损伤会导致感觉神经元功能紊乱,这是神经性疼痛发病机制的一个因素。然而,轴突横断的神经元与完整的相邻神经元的相对作用尚未明确。关键的第一步是确定部分神经损伤后这两种神经元群体的电生理变化。
在脊神经结扎(SNL)20天后,从轴突切断的第五腰段(L5)背根神经节神经元和相邻的完整L4神经元以及对照神经元和接受假SNL手术的其他神经元进行细胞内记录。
SNL后仅在L5神经元中观察到明显的电生理变化。Aα/β和Aδ两种神经元类型均表现出动作电位持续时间增加、超极化后电位幅度和持续时间减小以及动作电位起始电流阈值降低。Aα/β神经元表现出静息膜电位去极化,Aδ神经元在持续去极化过程中重复放电增加。轴突切断后,具有C纤维的神经元的超极化后电位持续时间缩短。与轴突切断的L5神经元不同,相邻的L4神经元在SNL后动作电位持续时间、超极化后电位参数或兴奋性没有变化。SNL后,L4的Aα/β和Aδ神经元的去极化速率(dV/dt)增加,但L5神经元中降低。与L5相比,SNL后L4的Aα/β神经元在超极化电流注入期间(下垂)的时间依赖性整流更大。假SNL手术仅使Aα/β神经元的输入电阻降低,中等大小细胞的传导速度降低。在轴突切断后的L5神经节中,一组新的神经元,占髓鞘化群体的24%,尽管髓鞘化神经元传导速度正常,但表现出长动作电位持续时间,特别是静息膜电位去极化、低去极化速率和无下垂。
这些发现表明,神经损伤诱导的电不稳定性仅限于轴突切断的神经元,相邻的完整神经元中不存在。