García-Alías Guillermo, Truong Kevin, Shah Prithvi K, Roy Roland R, Edgerton V Reggie
Department of Integrative Biology and Physiology, University of California, Los Angeles, USA.
Department of Integrative Biology and Physiology, University of California, Los Angeles, USA.
Exp Neurol. 2015 Apr;266:112-9. doi: 10.1016/j.expneurol.2015.01.009. Epub 2015 Feb 7.
The corticospinal and rubrospinal tracts are the predominant tracts for controlling skilled hand function. Injuries to these tracts impair grasping but not gross motor functions such as overground locomotion. The aim of the present study was to determine whether or not, after damage to both the corticospinal and rubrospinal tracts, other spared subcortical motor pathway can mediate the recovery of skilled hand function. Adult rats received a bilateral injury to the corticospinal tract at the level of the medullar pyramids and a bilateral ablation of the rubrospinal axons at C4. One group of rats received, acutely after injury, two injections of chondroitinase-ABC at C7, and starting at 7days post-injury were enrolled in daily reaching and grasping rehabilitation (CHASE group, n=5). A second group of rats received analogous injections of ubiquitous penicillinase, and did not undergo rehabilitation (PEN group, n=5). Compared to rats in the PEN group, CHASE rats gradually recovered the ability to reach and grasp over 42days after injury. Overground locomotion was mildly affected after injury and both groups followed similar recovery. Since the reticulospinal tract plays a predominant role in motor control, we further investigated whether or not plasticity of this pathway could contribute to the animal's recovery. Reticulospinal axons were anterogradely traced in both groups of rats. The density of reticulospinal processes in both the normal and ectopic areas of the grey ventral matter of the caudal segments of the cervical spinal cord was greater in the CHASE than PEN group. The results indicate that after damage to spinal tracts that normally mediate the control of reaching and grasping in rats other complementary spinal tracts can acquire the role of those damaged tracts and promote task-specific recovery.
皮质脊髓束和红核脊髓束是控制手部精细功能的主要神经束。这些神经束受损会损害抓握能力,但不会影响诸如地面行走等粗大运动功能。本研究的目的是确定在皮质脊髓束和红核脊髓束均受损后,其他未受损的皮质下运动通路是否能介导手部精细功能的恢复。成年大鼠在延髓锥体水平接受双侧皮质脊髓束损伤,并在C4水平进行双侧红核脊髓轴突切断术。一组大鼠在损伤后立即于C7处注射两次软骨素酶ABC,并在损伤后7天开始每天进行够物和抓握康复训练(CHASE组,n = 5)。另一组大鼠接受类似的普遍青霉素酶注射,且不进行康复训练(PEN组,n = 5)。与PEN组大鼠相比,CHASE组大鼠在损伤后42天内逐渐恢复了够物和抓握能力。损伤后地面行走受到轻度影响,两组恢复情况相似。由于网状脊髓束在运动控制中起主要作用,我们进一步研究了该通路的可塑性是否有助于动物的恢复。对两组大鼠的网状脊髓轴突进行了顺行示踪。在颈髓尾段灰质腹侧的正常和异位区域,CHASE组的网状脊髓突密度均高于PEN组。结果表明,在正常情况下介导大鼠够物和抓握控制的脊髓神经束受损后,其他互补脊髓神经束可发挥受损神经束的作用,促进特定任务的恢复。