Department of Neurobiology & Behavior, University of California at Irvine, Irvine, CA 92697, USA.
Exp Neurol. 2012 Feb;233(2):693-707. doi: 10.1016/j.expneurol.2011.08.011. Epub 2011 Nov 10.
It has previously been reported that a single dose of amphetamine paired with training on a beam walking task can enhance locomotor recovery following brain injury (Feeney et al., 1982). Here, we investigated whether this same drug/training regimen could enhance functional recovery following either thoracic (T9) or cervical (C5) spinal cord injury. Different groups of female Sprague-Dawley rats were trained on a beam walking task, and in a straight alley for assessment of hindlimb locomotor recovery using the BBB locomotor scale. For rats that received C5 hemisections, forelimb grip strength was assessed using a grip strength meter. Three separate experiments assessed the consequences of training rats on the beam walking task 24 h following a thoracic lateral hemisection with administration of either amphetamine or saline. Beginning 1 h following drug administration, rats either received additional testing/retraining on the beam hourly for 6 h, or they were returned to their home cages without further testing/retraining. Rats with thoracic spinal cord injuries that received amphetamine in conjunction with testing/retraining on the beam at 1 day post injury (DPI) exhibited significantly impaired recovery on the beam walking task and BBB. Rats with cervical spinal cord injuries that received training with amphetamine also exhibited significant impairments in beam walking and locomotion, as well as impairments in gripping and reaching abilities. Even when administered at 14 DPI, the drug/training regimen significantly impaired reaching ability in cervical spinal cord injured rats. Impairments were not seen in rats that received amphetamine without training. Histological analyses revealed that rats that received training with amphetamine had significantly larger lesions than saline controls. These data indicate that an amphetamine/training regimen that improves recovery after cortical injury has the opposite effect of impairing recovery following spinal cord injury because early training with amphetamine increases lesion severity.
先前有报道称,单次给予安非他命并结合在平衡木行走任务上进行训练,可增强脑损伤后的运动功能恢复(Feeney 等人,1982 年)。在此,我们研究了相同的药物/训练方案是否可以增强胸段(T9)或颈段(C5)脊髓损伤后的功能恢复。不同组别的雌性 Sprague-Dawley 大鼠在平衡木行走任务和直道上接受训练,以使用 BBB 运动评分评估后肢运动功能恢复情况。对于接受 C5 半切的大鼠,使用握力计评估前肢握力。三个单独的实验评估了在胸段侧半切后 24 小时,给予安非他命或生理盐水后,训练大鼠在平衡木行走任务上的后果。在药物给药后 1 小时开始,大鼠要么每小时接受额外的测试/再训练,总共 6 小时,要么返回其笼中,不再进行测试/再训练。在损伤后 1 天(DPI)接受安非他命联合测试/再训练的胸段脊髓损伤大鼠,在平衡木行走任务和 BBB 上的恢复明显受损。接受安非他命训练的颈段脊髓损伤大鼠,在平衡木行走和运动功能以及抓握和伸展能力方面也出现明显障碍。即使在 14 DPI 给予药物/训练方案,也会显著损害颈段脊髓损伤大鼠的伸展能力。未接受训练的大鼠未出现障碍。组织学分析显示,接受安非他命训练的大鼠的损伤明显大于生理盐水对照组。这些数据表明,在皮质损伤后改善恢复的安非他命/训练方案对脊髓损伤后的恢复有相反的影响,因为早期的安非他命训练会增加损伤的严重程度。