Tatsumi Atsuyoshi, Watanabe Kensuke
Department of Otorhinolaryngology, Dokkyo University School of Medicine, Koshigaya Hospital, Koshigaya, Japan.
Ann Otol Rhinol Laryngol. 2005 May;114(5):404-10. doi: 10.1177/000348940511400513.
When electron microscopy is performed on organs such as the inner ear that cannot be removed immediately after decapitation of animals, it is necessary to fix the target organ or tissue by systemic or regional perfusion fixation. However, such methods of fixation can increase vascular pressure or perilymphatic pressure, making it difficult to perform precise morphological observation of the vascular endothelial cells and membranous labyrinth. We recently attempted fixation of the cochlea by microwave irradiation. Guinea pigs were decapitated. The bullas were then removed from each animal and fixed in a mixture of 2% paraformaldehyde and 0.5% glutaraldehyde. Microwave (300 W) irradiation was then applied to the specimen for 1 minute. The fixative was immediately replaced with new fixative (4 degrees C). This sequence of manipulations was repeated 10 times, for a cumulative microwave irradiation time of 10 minutes. During the microwave irradiation period, the fixative temperature was kept at about 30 degrees C. After the last round of irradiation, the specimens were kept immersed in the fixative for 1 hour. After a small slit was created in the bone on the lateral wall of the cochlea, the specimens were post-fixed in osmic acid and embedded in Epon 812. Each specimen was cut into halves along the plane containing the modiolus of the cochlea. After the bone on the lateral wall of the cochlea was cut off under a stereoscopic microscope, ultrathin sections were prepared for observation under a transmission electron microscope. With this technique, the stria vascularis and the organ of Corti were fixed to a degree comparable to or better than that achieved with the conventional method of fixation. Fixation with microwave irradiation is relatively simple and can solve the problems associated with perfusion fixation, and thus provides an excellent means of fixation. This technique appears to be particularly promising for fixation for soft tissue surrounded by bone.
当对动物断头后不能立即取出的器官(如内耳)进行电子显微镜检查时,有必要通过全身或局部灌注固定来固定目标器官或组织。然而,这种固定方法会增加血管压力或外淋巴压力,从而难以对血管内皮细胞和膜迷路进行精确的形态学观察。我们最近尝试通过微波辐射固定耳蜗。将豚鼠断头。然后从每只动物身上取出颞骨泡并固定在2%多聚甲醛和0.5%戊二醛的混合液中。然后对标本施加微波(300瓦)辐射1分钟。立即用新的固定液(4℃)替换固定液。这个操作序列重复10次,累积微波辐射时间为10分钟。在微波辐射期间,固定液温度保持在约30℃。最后一轮辐射后,将标本浸泡在固定液中1小时。在耳蜗外侧壁的骨上切一个小切口后,将标本用锇酸后固定并包埋在Epon 812中。每个标本沿包含耳蜗蜗轴的平面切成两半。在立体显微镜下切下耳蜗外侧壁的骨后,制备超薄切片用于透射电子显微镜观察。用这种技术,血管纹和柯蒂器的固定程度与传统固定方法相当或更好。微波辐射固定相对简单,可以解决与灌注固定相关的问题,因此提供了一种极好的固定方法。这种技术对于固定被骨包围的软组织似乎特别有前景。