Department of Neurology, University of Cincinnati, Cincinnati, OH 45267, USA.
Eur J Neurosci. 2010 Oct;32(7):1092-9. doi: 10.1111/j.1460-9568.2010.07416.x.
In this review we outline some relevant considerations with regards to the rat model of deep brain stimulation of the subthalamic nucleus (STN DBS). In order to optimize the rat STN DBS model in terms of predictive validity for the clinical situation we propose that the STN stimulation experimental design parameters in rodents should incorporate the following features: (i) stimulation parameters that demonstrate functional alleviation of symptoms induced by nigrostriatal dopamine (DA) denervation; (ii) stimulation duration that is relatively long-term and continuous; (iii) stimulation that is initiated at a time when the denervation status of the nigrostriatal system is known to be partial and progressing; (iv) stimulation current spread that is minimized and optimized to closely approximate the clinical situation; (v) the appropriate control conditions are included; and (vi) implantation to the STN target is verified post-mortem. Further research that examines the effect of long-term STN DBS on the neurophysiology and neurochemistry of STN circuitry is warranted. The rat model of functionally relevant long-term STN DBS provides a most favorable preclinical experimental platform in which to conduct these studies.
在这篇综述中,我们概述了一些与亚丘脑核(STN)深部脑刺激的大鼠模型相关的考虑因素。为了优化大鼠 STN DBS 模型在预测临床情况方面的有效性,我们建议啮齿动物的 STN 刺激实验设计参数应包含以下特征:(i)刺激参数应能证明对黑质纹状体多巴胺(DA)去神经支配引起的症状有功能缓解作用;(ii)刺激持续时间相对较长且连续;(iii)刺激应在黑质纹状体系统的去神经支配状态已知为部分和进展的情况下开始;(iv)刺激电流传播应最小化并优化,以接近临床情况;(v)应包括适当的对照条件;(vi)植入 STN 目标后应进行死后验证。进一步研究长期 STN DBS 对 STN 电路的神经生理学和神经化学的影响是必要的。具有功能相关性的长期 STN DBS 的大鼠模型为进行这些研究提供了最有利的临床前实验平台。