School of Kinesiology and Nutritional Science, California State University, Los Angeles, California 90032-8162, USA.
J Neurotrauma. 2011 Jun;28(6):1021-33. doi: 10.1089/neu.2010.1699. Epub 2011 Jun 9.
Intensive weight-supported treadmill training (WSTT) improves locomotor function following spinal cord injury. Because of a number of factors, undergoing intensive sessions of training may not be feasible. Whether reduced amounts of training are sufficient to enhance spinal plasticity to a level that is necessary for improving function is not known. The focus of the present study was to assess differences in recovery of locomotor function and spinal plasticity as a function of the amount of steps taken during WSTT in a rodent model of spinal cord injury. Rats were spinally transected at 5 days of age. When they reached 28 days of age, a robotic system was used to implement a weight-supported treadmill training program of either 100 or 1000 steps/training session daily for 4 weeks. Antibodies for brain-derived neurotrophic factor (BDNF), TrkB, and the pre-synaptic marker, synaptophysin, were used to examine the expression of these proteins in the ventral horn of the lumbar spinal cord. Rats that received weight-supported treadmill training performed better stepping relative to untrained rats, but only the rats that received 1000 steps/training session recovered locomotor function that resembled normal patterns. Only the rats that received 1000 steps/training session recovered normal levels of synaptophysin immunoreactivity around motor neurons. Weight-supported treadmill training consisting of either 100 or 1000 steps/training session increased BDNF immunoreactivity in the ventral horn of the lumbar spinal cord. TrkB expression in the ventral horn was not affected by spinal cord transection or weight-supported treadmill training. Synaptophysin expression, but not BDNF or TrkB expression was correlated with the recovery of stepping function. These findings suggested that a large amount of weight-supported treadmill training was necessary for restoring synaptic connections to motor neurons within the locomotor generating circuitry. Although a large amount of training was best for recovery, small amounts of training were associated with incremental gains in function and increased BDNF levels.
强化体重支持式跑步机训练(WSTT)可改善脊髓损伤后的运动功能。由于多种因素,密集的训练课程可能不可行。进行较少的训练量是否足以增强脊髓可塑性,达到改善功能所需的水平尚不清楚。本研究的重点是评估在脊髓损伤的啮齿动物模型中,WSTT 期间所走步数对运动功能恢复和脊髓可塑性的影响。大鼠在出生后 5 天进行脊髓横断。当它们达到 28 天时,使用机器人系统实施每日 100 或 1000 步/训练疗程的体重支持式跑步机训练方案,持续 4 周。使用脑源性神经营养因子(BDNF)、TrkB 和突触前标记物突触小体蛋白的抗体来检查这些蛋白质在腰骶脊髓腹角中的表达。进行体重支持式跑步机训练的大鼠相对于未训练的大鼠表现出更好的步幅,但只有接受 1000 步/训练疗程的大鼠恢复了类似于正常模式的运动功能。只有接受 1000 步/训练疗程的大鼠恢复了运动神经元周围正常水平的突触小体蛋白免疫反应性。由 100 或 1000 步/训练疗程组成的体重支持式跑步机训练增加了腰骶脊髓腹角中的 BDNF 免疫反应性。脊髓横断或体重支持式跑步机训练对腹角中的 TrkB 表达没有影响。突触小体蛋白表达,但不是 BDNF 或 TrkB 表达与步幅功能的恢复相关。这些发现表明,大量的体重支持式跑步机训练对于恢复运动产生电路中的运动神经元的突触连接是必要的。尽管大量训练最有利于恢复,但少量训练与功能的增量增益和 BDNF 水平的增加相关。