Seifert E, Schadel A, Theilen H
Poliklinik für Phoniatrie und Pädaudiologie, Universität Münster.
HNO. 1994 Apr;42(4):224-8.
At the present time there is no final explanation for the etiology of Bell's palsy. The theory of pathophysiology involving a combined primary and/or secondary ischemia is now well-accepted. As such, it is supposed that there is a dysfunction of the blood vessels which supply the nerve. This is followed by a hyperpermeability and transudation which lead to edema of the nerve and compression of the blood supply. The vicious circle starts and the final result is facial paralysis. The blood supply of the facial nerve has been described previously in the literature, although there have been no experimental investigations on in vivo perfusion of the nerve. In the present study we evaluated the percentage of those vessels perfused among the total blood vessels found in facial nerves of Wistar rats. Animals were examined after i.v.-injections of Evans blue dye, with perfused vessels demonstrable under a fluorescence microscope. Forty-eight hours later, the same tissue section was stained by indirect immunofluorescence and the primary antibody used was directed against myosin of non-muscle sources. This antibody cross-reacted with myosin of vascular endothelial cells and thus allowed identification of any existing blood vessels. More than 90% of the immunostained vessels were labeled with the dye, showing that almost all vessels were perfused.
目前,贝尔麻痹的病因尚无最终解释。涉及原发性和/或继发性缺血合并的病理生理学理论现已被广泛接受。因此,推测供应神经的血管存在功能障碍。随后会出现通透性增加和渗出,导致神经水肿并压迫血液供应。恶性循环由此开始,最终结果是面部瘫痪。面神经的血液供应此前已有文献描述,尽管尚未有关于神经体内灌注的实验研究。在本研究中,我们评估了在Wistar大鼠面神经中发现的总血管中被灌注血管的百分比。在静脉注射伊文思蓝染料后对动物进行检查,可在荧光显微镜下显示被灌注的血管。48小时后,对同一组织切片进行间接免疫荧光染色,使用的一抗针对非肌肉来源的肌球蛋白。该抗体与血管内皮细胞的肌球蛋白发生交叉反应,从而能够识别任何现存的血管。超过90%的免疫染色血管被染料标记,表明几乎所有血管都被灌注。