Cerón Jeimmy, Troncoso Julieta
Laboratorio de Neurofisiología Comportamental, Departamento de Ciencias Fisiológicas, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá, D.C., Colombia.
Biomedica. 2016 Dec 1;36(4):619-631. doi: 10.7705/biomedica.v36i4.3259.
Our research group has described both morphological and electrophysiological changes in motor cortex pyramidal neurons associated with contralateral facial nerve injury in rats. However, little is known about those neural changes, which occur together with changes in surrounding glial cells.
To characterize the effect of the unilateral facial nerve injury on microglial proliferation and activation in the primary motor cortex.
We performed immunohistochemical experiments in order to detect microglial cells in brain tissue of rats with unilateral facial nerve lesion sacrificed at different times after the injury. We caused two types of lesions: reversible (by crushing, which allows functional recovery), and irreversible (by section, which produces permanent paralysis). We compared the brain tissues of control animals (without surgical intervention) and sham-operated animals with animals with lesions sacrificed at 1, 3, 7, 21 or 35 days after the injury.
In primary motor cortex, the microglial cells of irreversibly injured animals showed proliferation and activation between three and seven days post-lesion. The proliferation of microglial cells in reversibly injured animals was significant only three days after the lesion.
Facial nerve injury causes changes in microglial cells in the primary motor cortex. These modifications could be involved in the generation of morphological and electrophysiological changes previously described in the pyramidal neurons of primary motor cortex that command facial movements.
我们的研究小组已经描述了与大鼠对侧面神经损伤相关的运动皮层锥体神经元的形态学和电生理学变化。然而,对于那些与周围神经胶质细胞变化同时发生的神经变化却知之甚少。
表征单侧面神经损伤对初级运动皮层中小胶质细胞增殖和激活的影响。
我们进行了免疫组织化学实验,以检测在损伤后不同时间处死的单侧面神经损伤大鼠脑组织中的小胶质细胞。我们造成了两种类型的损伤:可逆性损伤(通过挤压,可实现功能恢复)和不可逆性损伤(通过切断,会导致永久性麻痹)。我们将对照动物(无手术干预)和假手术动物的脑组织与在损伤后1、3、7、21或35天处死的损伤动物的脑组织进行了比较。
在初级运动皮层中,不可逆损伤动物的小胶质细胞在损伤后三天到七天之间出现增殖和激活。可逆损伤动物的小胶质细胞增殖仅在损伤后三天显著。
面神经损伤会导致初级运动皮层中小胶质细胞发生变化。这些改变可能与先前在控制面部运动的初级运动皮层锥体神经元中描述的形态学和电生理学变化的产生有关。