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首页> 外文期刊>Neuromodulation: journal of the International Neuromodulation Society >Mechanisms of Dorsal Root Ganglion Stimulation in Pain Suppression: A Computational Modeling Analysis
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Mechanisms of Dorsal Root Ganglion Stimulation in Pain Suppression: A Computational Modeling Analysis

机译:疼痛抑制中背根神经节刺激的机制:计算建模分析

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Objective The mechanisms of dorsal root ganglion (DRG) stimulation for chronic pain remain unclear. The objective of this work was to explore the neurophysiological effects of DRG stimulation using computational modeling. Methods Electrical fields produced during DRG stimulation were calculated with finite element models, and were coupled to a validated biophysical model of a C‐type primary sensory neuron. Intrinsic neuronal activity was introduced as a 4 Hz afferent signal or somatic ectopic firing. The transmembrane potential was measured along the neuron to determine the effect of stimulation on intrinsic activity across stimulation parameters, cell location/orientation, and membrane properties. Results The model was validated by showing close correspondence in action potential (AP) characteristics and firing patterns when compared to experimental measurements. Subsequently, the model output demonstrated that T‐junction filtering was amplified with DRG stimulation, thereby blocking afferent signaling, with cathodic stimulation at amplitudes of 2.8–5.5 × stimulation threshold and frequencies above 2 Hz. This amplified filtering was dependent on the presence of calcium and calcium‐dependent small‐conductance potassium channels, which produced a hyperpolarization offset in the soma, stem, and T‐junction with repeated somatic APs during stimulation. Additionally, DRG stimulation suppressed somatic ectopic activity by hyperpolarizing the soma with cathodic or anodic stimulation at amplitudes of 3–11 × threshold and frequencies above 2 Hz. These effects were dependent on the stem axon being relatively close to and oriented toward a stimulating contact. Conclusions These results align with the working hypotheses on the mechanisms of DRG stimulation, and indicate the importance of stimulation amplitude, polarity, and cell location/orientation on neuronal responses.
机译:目的对慢性疼痛的背根神经节(DRG)刺激的机制仍不清楚。这项工作的目的是利用计算建模探讨DRG刺激的神经生理学效果。方法使用有限元模型计算DRG刺激期间产生的电场,并耦合到C型初级感觉神经元的验证生物物理模型。将内在神经元活性作为4Hz传入信号或体细胞异位烧制引入。沿神经元测量跨膜电位,以确定刺激对刺激参数,细胞定位/取向和膜特性的内在活动的影响。结果通过在与实验测量相比,通过在动作电位(AP)特征和烧制模式中显示紧密对应来验证模型。随后,模型输出证明了用DRG刺激扩增T-结滤波,从而阻止传入信号传导,在幅度为2.8-5.5×刺激阈值和频率高于2Hz的刺激。该扩增的过滤依赖于钙和钙依赖性小导线的存在,其在刺激期间在SOMA,茎和T型连接中产生的超极化偏移,并在刺激期间具有重复的体细胞AP。另外,DRG刺激通过在3-11×阈值的幅度和2Hz以上的幅度为3-11×阈值和频率的幅度,通过将SOMA超渗透细胞体细胞体细胞异位活性。这些效果依赖于杆轴突相对接近并向刺激接触定向。结论这些结果与DRG刺激机制的工作假设对齐,并表明刺激幅度,极性和细胞位置/取向对神经元反应的重要性。

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