Povlishock J T, Rosenblum W I, Sholley M M, Wei E P
Am J Pathol. 1983 Feb;110(2):148-60.
Those microvascular endothelial events that parallel the evolution of platelet aggregation were evaluated in a well-controlled animal model. Cat pial microvessels were observed through a cranial window while local platelet aggregation was produced by intravenous injection of sodium fluorescein and simultaneous exposure of the pial vessels to light from a filtered mercury lamp that excited the fluorescein. The vessels were fixed in situ when the in vivo observations of a preselected vessel indicated early, intermediate, or advanced aggregation in that vessel. The preselected vessel was then harvested for ultrastructural study together with adjacent vessels from the illuminated field. These vessels and appropriate controls were compared in semiserial thin sections. The onset of platelet aggregation in both venules and arterioles was accompanied by focal endothelial lucency, vacuole formation, luminal membrane rupture, and swelling of the nuclear envelope. These changes were not found in control material. With intermediate aggregation these changes were more common, while with advanced aggregation these abnormalities occurred together with focal endothelial denudation. Thus, in this model denudation occurred only with advanced aggregation and was not a prerequisite for aggregation.
在一个严格控制的动物模型中,对那些与血小板聚集演变过程平行的微血管内皮事件进行了评估。通过颅骨视窗观察猫的软脑膜微血管,同时通过静脉注射荧光素钠诱导局部血小板聚集,并使软脑膜血管同时暴露于激发荧光素的过滤汞灯光线下。当对预先选定的血管进行体内观察显示该血管出现早期、中期或晚期聚集时,将血管原位固定。然后将预先选定的血管连同来自照明区域的相邻血管一起取材用于超微结构研究。在半连续超薄切片中对这些血管和适当的对照进行比较。小静脉和小动脉中血小板聚集的开始均伴有局部内皮细胞透亮、空泡形成、管腔膜破裂以及核膜肿胀。在对照材料中未发现这些变化。在中期聚集时,这些变化更为常见,而在晚期聚集时,这些异常与局部内皮剥脱同时出现。因此,在该模型中,内皮剥脱仅在晚期聚集时发生,并非聚集的先决条件。