Adkins DeAnna L, Hsu J Edward, Jones Theresa A
Institute for Neuroscience, University of Texas at Austin, TX 78712, USA.
Exp Neurol. 2008 Jul;212(1):14-28. doi: 10.1016/j.expneurol.2008.01.031. Epub 2008 Feb 20.
Cortical stimulation (CS) as a means to modulate regional activity and excitability in cortex is emerging as a promising approach for facilitating rehabilitative interventions after brain damage, including stroke. In this study, we investigated whether CS-induced functional improvements are linked with synaptic plasticity in peri-infarct cortex and vary with the severity of impairments. Adult rats that were proficient in skilled reaching received subtotal unilateral ischemic sensorimotor cortex (SMC) lesions and implantation of chronic epidural electrodes over remaining motor cortex. Based on the initial magnitude of reaching deficits, rats were divided into severely and moderately impaired subgroups. Beginning two weeks post-surgery, rats received 100 Hz cathodal CS at 50% of movement thresholds or no-stimulation control procedures (NoCS) during 18 days of rehabilitative training on a reaching task. Stereological electron microscopy methods were used to quantify axodendritic synapse subtypes in motor cortical layer V underlying the electrode. In moderately, but not severely impaired rats, CS significantly enhanced recovery of reaching success. Sensitive movement analyses revealed that CS partially normalized reaching movements in both impairment subgroups compared to NoCS. Additionally, both CS subgroups had significantly greater density of axodendritic synapses and moderately impaired CS rats had increases in presumed efficacious synapse subtypes (perforated and multiple synapses) in stimulated cortex compared to NoCS. Synaptic density was positively correlated with post-rehabilitation reaching success. In addition to providing further support that CS can promote functional recovery, these findings suggest that CS-induced functional improvements may be mediated by synaptic structural plasticity in stimulated cortex.
皮层刺激(CS)作为一种调节皮层区域活动和兴奋性的手段,正逐渐成为促进脑损伤(包括中风)后康复干预的一种有前景的方法。在本研究中,我们调查了CS诱导的功能改善是否与梗死灶周围皮层的突触可塑性相关,以及是否随损伤严重程度而变化。熟练掌握熟练抓握动作的成年大鼠接受了单侧大脑中动脉闭塞导致的部分缺血性感觉运动皮层(SMC)损伤,并在剩余运动皮层植入慢性硬膜外电极。根据最初抓握缺陷的严重程度,将大鼠分为重度和中度损伤亚组。术后两周开始,大鼠在进行18天的抓握任务康复训练期间,接受50%运动阈值的100Hz阴极CS刺激或无刺激对照程序(NoCS)。采用体视学电子显微镜方法对电极下方运动皮层V层的轴突树突突触亚型进行定量分析。在中度而非重度损伤的大鼠中,CS显著提高了抓握成功率的恢复。敏感运动分析表明,与NoCS相比,CS在两个损伤亚组中都部分使抓握动作正常化。此外,与NoCS相比,两个CS亚组的轴突树突突触密度均显著增加,中度损伤的CS大鼠在受刺激皮层中假定有效的突触亚型(穿孔突触和多个突触)增加且有增加趋势。突触密度与康复后抓握成功率呈正相关。这些发现除了进一步支持CS可以促进功能恢复外,还表明CS诱导的功能改善可能是由受刺激皮层中的突触结构可塑性介导的。