Adkins DeAnna L, Campos Peter, Quach David, Borromeo Mark, Schallert Kellan, Jones Theresa A
Institute for Neuroscience, University of Texas at Austin, 78712, USA.
Exp Neurol. 2006 Aug;200(2):356-70. doi: 10.1016/j.expneurol.2006.02.131. Epub 2006 May 6.
This study examined whether epidurally delivered cortical electrical stimulation (CS) improves the efficacy of motor rehabilitative training and alters neuronal density and/or cell proliferation in perilesion cortex following ischemic sensorimotor cortex (SMC) lesions. Adult rats were pre-trained on a skilled reaching task and then received partial unilateral SMC lesions and implantation of electrodes over the remaining SMC. Ten to fourteen days later, rats received daily reach training concurrent with anodal or cathodal 100 Hz CS or no stimulation (NoCS) for 18 days. To label newly generated cells, bromodeoxyuridine (BrdU; 50 mg/kg) was administered every third day of training. Both anodal and cathodal CS robustly enhanced reaching performance compared to NoCS controls. Neuronal density in the perilesion cortex was significantly increased in the cathodal CS group compared to the NoCS group. There were no significant group differences in BrdU-labeled cell density in ipsilesional cortex. Staining with Fluoro-Jade-B indicated that neurons continue to degenerate near the infarct at the time when cortical stimulation and rehabilitation were initiated. These data indicate that epidurally delivered CS greatly improves the efficacy of rehabilitative reach training following SMC damage and raise the possibility that cathodal CS may influence neuronal survival in perilesion cortex.
本研究探讨硬膜外给予皮层电刺激(CS)是否能提高运动康复训练的效果,并改变缺血性感觉运动皮层(SMC)损伤后损伤周围皮层的神经元密度和/或细胞增殖。成年大鼠在熟练抓握任务上进行预训练,然后接受部分单侧SMC损伤,并在剩余的SMC上植入电极。10至14天后,大鼠接受每日抓握训练,同时接受阳极或阴极100Hz CS刺激或不接受刺激(无CS),持续18天。为了标记新生成的细胞,在训练的每第三天给予溴脱氧尿苷(BrdU;50mg/kg)。与无CS对照组相比,阳极和阴极CS均显著提高了抓握能力。与无CS组相比,阴极CS组损伤周围皮层的神经元密度显著增加。同侧皮层中BrdU标记的细胞密度在各实验组之间无显著差异。Fluoro-Jade-B染色表明,在开始皮层刺激和康复训练时,梗死灶附近的神经元仍在退化。这些数据表明,硬膜外给予CS可显著提高SMC损伤后康复抓握训练的效果,并增加阴极CS可能影响损伤周围皮层神经元存活的可能性。