Neuroscience Graduate Program, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Department of Anatomy, Physiology, and Genetics, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA.
Behav Brain Res. 2021 May 7;405:113210. doi: 10.1016/j.bbr.2021.113210. Epub 2021 Feb 24.
Gait disruptions following traumatic brain injury (TBI) are noted in the clinical population. To date, thorough analysis of gait changes in animal models of TBI to allow for correlation of pathological alterations and utilization of this as a therapeutic outcome have been limited. We therefore assessed gait using the DigiGait analysis system as well as overall locomotion using the Beam Walk test in adult male Sprague-Dawley rats following a commonly used model of TBI, parietal lobe controlled cortical impact (CCI). Rats underwent DigiGait baseline analysis 24 h prior to injury, followed by a moderate CCI in the left parietal lobe. Performance on the DigiGait was then assessed at 1, 3, 7, and 14 days post-injury, followed by histological analysis of brain tissue. Beam walk analysis showed a transient but significant impairment acutely after injury. Despite observance of gait disturbance in the clinical population, TBI in the parietal lobe of rats resulted in limited alterations in hind or forelimb function. General hindlimb locomotion showed significant but transient impairment. Significant changes in gait were observed to last through the sub-acute period, including right hindpaw angle of rotation and left forelimb and right hindlimb swing phase duration. Slight changes that did not reach statistical significant but may reflect subtle impacts of TBI on gait were reflected in several other measures, such as stride duration, stance duration and stance width. These results demonstrate that moderate-severe injury to the parietal cortex and underlying structures including corpus callosum, hippocampus, thalamus and basal ganglia result in slight changes to gait that can be detected using the Digigait analysis system.
创伤性脑损伤 (TBI) 后会出现步态障碍,这在临床人群中已有报道。迄今为止,对 TBI 动物模型中的步态变化进行了彻底分析,以允许对病理改变进行相关性分析,并将其用作治疗结果,但利用这种方法的研究还很有限。因此,我们使用 DigiGait 分析系统评估了步态,并用 Beam Walk 测试评估了成年雄性 Sprague-Dawley 大鼠整体运动,这些大鼠在经历了一种常用的 TBI 模型——顶叶皮质控制的皮质撞击 (CCI) 后进行了研究。大鼠在受伤前 24 小时进行了 DigiGait 基线分析,然后在左顶叶进行了中度 CCI。在受伤后 1、3、7 和 14 天,我们对 DigiGait 的表现进行了评估,随后对脑组织进行了组织学分析。Beam Walk 分析显示,受伤后急性阶段存在短暂但显著的损伤。尽管在临床人群中观察到步态障碍,但大鼠顶叶的 TBI 导致后肢或前肢功能的改变有限。一般后肢运动表现出显著但短暂的损伤。通过亚急性期观察到步态的明显变化,包括右后足旋转角度以及左前肢和右后肢摆动阶段持续时间。在几个其他指标中也观察到了一些细微的变化,但没有达到统计学意义,但可能反映了 TBI 对步态的细微影响,例如步幅持续时间、站立持续时间和站立宽度。这些结果表明,顶叶皮质以及包括胼胝体、海马体、丘脑和基底神经节在内的深部结构的中重度损伤,会导致使用 DigiGait 分析系统可以检测到的轻微步态变化。