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Altered excitability of small cutaneous nerve fibers during cooling assessed with the perception threshold tracking technique

机译:感知阈值跟踪技术评估冷却过程中小皮肤神经纤维的兴奋性改变

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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: NaTTXs, NaTTXr, NaP, KDr, KM, KLeak, KA, 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 KLeak channel and the Na/K-ATPase. For short durations, the effect cancels out due to a reduction of the transient TTX resistant sodium current (Nav1.8). 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.
机译:需要新的方法来增加健康受试者以及病理状况期间小神经纤维的膜兴奋性的知识。我们的研究小组以前已经开发了感知阈值跟踪技术,以间接评估周围小神经纤维的膜特性。在当前的研究中,评估了一种通过冷却小纤维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。第一个目标是检查感知阈值跟踪技术是否可以检测到冷却过程中改变的兴奋性。第二个目标是对潜在的离子电流进行计算建模,该离子电流可能是冷诱导的小纤维兴奋性改变的原因。第三个目标是评估冷却和电模拟的计算模型是否可用于生成小纤维神经病中离子电流变化的假设。通过感知阈值跟踪技术对两种温度条件(20°C和32°C)评估小纤维的兴奋性。开发了详细的多室模型,包括离子电流:NaTTXs,NaTTXr,NaP,KDr,KM,KLeak,KA和Na / K-ATPase。当皮肤温度从32°C降低到20°C时,两个长时间脉冲(50和100?ms)的感知阈值降低(p <0.001)。但是,对于较短的持续时间(1?ms,p?=?0.116; 5?ms p?=?0.079,rmANOVA,Sidak)没有观察到明显的影响。该计算模型预测,与长时间脉冲相关的感知阈值的降低可能源自KLeak通道和Na / K-ATPase的降低。在短时间内,由于抗TTX的瞬态钠电流(Nav1.8)的减小,该效果抵消了。另外,计算模型的结果表明,冷却与电刺激同时进行,可以增加有关离子电流病理改变的知识。冷却可在电刺激过程中改变离子电流,从而提供有关健康受试者中细纤维的膜兴奋性以及潜在地在病理状况下的其他信息。

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