Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA; Biointerfaces Institute, University of Michigan, Ann Arbor, MI, USA.
Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Clin Neurophysiol. 2019 Jun;130(6):941-951. doi: 10.1016/j.clinph.2019.02.016. Epub 2019 Mar 15.
The goal of this project was to use computational models to investigate which types of primary sensory neurons are modulated by dorsal root ganglion stimulation (DRGS) to provide pain relief.
We modeled DRGS by coupling an anatomical finite element model of a human L5 dorsal root ganglion to biophysical models of primary sensory neurons. We calculated the stimulation amplitude needed to elicit an action potential in each neuron, and examined how DRGS affected sensory neuron activity.
We showed that within clinical ranges of stimulation parameters, DRGS drives the activity of large myelinated Aβ-fibers but does not directly activate small nonmyelinated C-fibers. We also showed that the position of the active and return electrodes and the polarity of the stimulus pulse influence neural activation.
Our results indicate that DRGS may provide pain relief by activating pain-gating mechanisms in the dorsal horn via repeated activation of large myelinated afferents.
Understanding the mechanisms of action of DRGS-induced pain relief may lead to innovations in stimulation technologies that improve patient outcomes.
本项目旨在使用计算模型研究哪种类型的初级感觉神经元会受到背根神经节刺激(DRGS)的调节,以提供疼痛缓解。
我们通过将人体 L5 背根神经节的解剖有限元模型与初级感觉神经元的生物物理模型相结合来模拟 DRGS。我们计算了引起每个神经元动作电位所需的刺激幅度,并研究了 DRGS 如何影响感觉神经元的活动。
我们表明,在临床刺激参数范围内,DRGS 驱动大有髓 Aβ纤维的活动,但不会直接激活小无髓 C 纤维。我们还表明,活动和返回电极的位置以及刺激脉冲的极性会影响神经激活。
我们的结果表明,DRGS 可能通过通过反复激活大的有髓传入纤维来激活背角中的疼痛门控机制来提供疼痛缓解。
了解 DRGS 诱导的疼痛缓解的作用机制可能会导致刺激技术的创新,从而改善患者的治疗效果。