Hugosdottir Rosa, Mørch Carsten Dahl, Jørgensen Cecilia Klitgaard, Nielsen Camilla Winther, Olsen Mathias Vassard, Pedersen Mads Jozwiak, Tigerholm Jenny
Center of Neuroplasticity and Pain, SMI®, Department of Health Science and Technology, Aalborg University, Fredrik Bajers Vej 7D3, 9220, Aalborg, Denmark.
BMC Neurosci. 2019 Sep 3;20(1):47. doi: 10.1186/s12868-019-0527-3.
There is a need for new approaches to increase the knowledge of the membrane excitability of small nerve fibers both in healthy subjects, as well as during pathological conditions. Our research group has previously developed the perception threshold tracking technique to indirectly assess the membrane properties of peripheral small nerve fibers. In the current study, a new approach for studying membrane excitability by cooling small fibers, simultaneously with applying a slowly increasing electrical stimulation current, is evaluated. The first objective was to examine whether altered excitability during cooling could be detected by the perception threshold tracking technique. The second objective was to computationally model the underlying ionic current that could be responsible for cold induced alteration of small fiber excitability. The third objective was to evaluate whether computational modelling of cooling and electrical simulation can be used to generate hypotheses of ionic current changes in small fiber neuropathy.
The excitability of the small fibers was assessed by the perception threshold tracking technique for the two temperature conditions, 20 °C and 32 °C. A detailed multi-compartment model was developed, including the ionic currents: Na, Na, Na, K, K, K, K, and Na/K-ATPase. The perception thresholds for the two long duration pulses (50 and 100 ms) were reduced when the skin temperature was lowered from 32 to 20 °C (p < 0.001). However, no significant effects were observed for the shorter durations (1 ms, p = 0.116; 5 ms p = 0.079, rmANOVA, Sidak). The computational model predicted that the reduction in the perception thresholds related to long duration pulses may originate from a reduction of the K channel and the Na/K-ATPase. For short durations, the effect cancels out due to a reduction of the transient TTX resistant sodium current (Na1.8). Additionally, the result from the computational model indicated that cooling simultaneously with electrical stimulation, may increase the knowledge regarding pathological alterations of ionic currents.
Cooling may alter the ionic current during electrical stimulation and thereby provide additional information regarding membrane excitability of small fibers in healthy subjects and potentially also during pathological conditions.
需要新的方法来增加对健康受试者以及病理状态下小神经纤维膜兴奋性的了解。我们的研究小组先前已开发出感知阈值跟踪技术,以间接评估外周小神经纤维的膜特性。在当前研究中,评估了一种通过冷却小纤维并同时施加缓慢增加的电刺激电流来研究膜兴奋性的新方法。第一个目标是研究感知阈值跟踪技术是否能检测到冷却过程中兴奋性的改变。第二个目标是通过计算模拟可能导致小纤维兴奋性冷诱导改变的潜在离子电流。第三个目标是评估冷却和电刺激的计算模型是否可用于生成小纤维神经病变中离子电流变化的假设。
通过感知阈值跟踪技术评估了20°C和32°C这两种温度条件下小纤维的兴奋性。开发了一个详细的多室模型,包括离子电流:Na、Na、Na、K、K、K、K和Na/K-ATP酶。当皮肤温度从32°C降至20°C时,两个长持续时间脉冲(50和100毫秒)的感知阈值降低(p < 0.001)。然而,对于较短持续时间(1毫秒,p = 0.116;5毫秒,p = 0.079,重复测量方差分析,Sidak检验)未观察到显著影响。计算模型预测,与长持续时间脉冲相关的感知阈值降低可能源于K通道和Na/K-ATP酶的减少。对于短持续时间,由于瞬时耐河豚毒素钠电流(Na1.8)的减少,这种影响相互抵消。此外,计算模型的结果表明,冷却与电刺激同时进行,可能会增加有关离子电流病理改变的知识。
冷却可能会在电刺激过程中改变离子电流,从而提供有关健康受试者以及潜在病理状态下小纤维膜兴奋性的额外信息。