Brown Samuel P, Lawson Ryan J, Moreno Jonathan D, Ransdell Joseph L
Department of Biology, Miami University, Oxford, OH 45056.
Division of Cardiology, Department of Medicine, Washington University in St. Louis, St. Louis, MO 63130.
bioRxiv. 2024 Jun 1:2023.10.25.564042. doi: 10.1101/2023.10.25.564042.
The resurgent sodium current (I) activates on membrane repolarization, such as during the downstroke of neuronal action potentials. Due to its unique activation properties, I is thought to drive high rates of repetitive neuronal firing. However, I is often studied in combination with the persistent or non-inactivating portion of sodium currents (I). We used dynamic clamp to test how I and I individually affect repetitive firing in adult cerebellar Purkinje neurons from male and female mice. We learned I does not scale repetitive firing rates due to its rapid decay at subthreshold voltages, and that subthreshold I is critical in regulating neuronal firing rate. Adjustments to the Nav conductance model used in these studies revealed I and I can be inversely scaled by adjusting occupancy in the slow inactivated kinetic state. Together with additional dynamic clamp experiments, these data suggest the regulation of sodium channel slow inactivation can fine-tune I and Purkinje neuron repetitive firing rates.
复苏钠电流(I)在膜复极化时激活,比如在神经元动作电位的下降支期间。由于其独特的激活特性,I被认为驱动神经元的高频重复放电。然而,I通常是与钠电流的持续或非失活部分(I)一起研究的。我们使用动态钳来测试I和I分别如何影响成年雄性和雌性小鼠小脑浦肯野神经元的重复放电。我们了解到I由于其在阈下电压下的快速衰减而不会调节重复放电率,并且阈下I在调节神经元放电率方面至关重要。对这些研究中使用的Nav电导模型的调整表明,通过调整慢失活动力学状态的占有率,I和I可以呈反比缩放。连同其他动态钳实验,这些数据表明钠通道慢失活的调节可以微调I和浦肯野神经元的重复放电率。