Pluta R, Lossinsky A S, Walski M, Wisniewski H M, Mossakowski M J
Department of Neuropathology, Medical Research Centre, Polish Academy of Sciences, Warsaw.
J Hirnforsch. 1994;35(4):463-71.
Platelet interaction with cerebral microvessels was studied in rats after global brain ischemia. Studies were performed with a model of global central nervous system ischemia produced by cardiocirculatory arrest in normothermic rats. The ischemic period of 5-min was followed by times of recirculation lasting 5 and 15 mins, 1, 3, 6, 24, and 48 hrs, and 6, 10, and 12 months. After different periods of survival, blood vessels from brains were examined by transmission electron microscopy. Our investigation revealed numerous platelet aggregates of varying sizes within both arterial and venous intraparenchymal vessels. At the same time, we also noted platelets in various stages of disintegration. Platelets close to the endothelial cells were often degranulated, with shape changes including pseudopodia. Aggregates of platelets were focal, random, and more widespread occurring in the cerebral cortex, thalamus, basal ganglia, hippocampus, and cerebellum. We also observed recent aggregates of platelets and thrombi, which presented varying degrees of degranulation. In one time period, some platelets were found outside the brain vessels (in the perivascular space after 24 hrs of survival). We present evidence that platelet aggregation was repeated a long time after the ischemic incident, i.e., after one year. The main result was a prominent and local accumulation of platelets in microvessel branches or regions of vessel bifurcations, which correlated well with blood-brain barrier alterations observed previously in this model. The platelet aggregations increased in frequency with longer periods of recirculation. We noted that local platelet adhesion/aggregation was present after brain ischemia requiring no denudation or exposure of the basal lamina.(ABSTRACT TRUNCATED AT 250 WORDS)
在全脑缺血后的大鼠中研究了血小板与脑微血管的相互作用。研究采用了在常温大鼠中通过心脏循环骤停产生的全中枢神经系统缺血模型。5分钟的缺血期后,再灌注时间分别为5分钟、15分钟、1小时、3小时、6小时、24小时、48小时以及6个月、10个月和12个月。在不同存活期后,通过透射电子显微镜检查脑内血管。我们的研究发现,在脑实质内的动脉和静脉血管中存在大量大小各异的血小板聚集体。同时,我们还注意到处于不同解体阶段的血小板。靠近内皮细胞的血小板常常脱颗粒,形状发生改变,包括出现伪足。血小板聚集体呈局灶性、随机分布,在大脑皮层、丘脑、基底神经节、海马体和小脑中更为广泛。我们还观察到近期形成的血小板聚集体和血栓,它们呈现出不同程度的脱颗粒。在一个时间段内,发现一些血小板位于脑血管外(存活24小时后在血管周围间隙)。我们提供的证据表明,在缺血事件后很长时间,即一年后,血小板聚集仍会反复发生。主要结果是血小板在微血管分支或血管分叉区域显著局部积聚,这与该模型先前观察到的血脑屏障改变密切相关。随着再灌注时间延长,血小板聚集频率增加。我们注意到脑缺血后存在局部血小板黏附/聚集,且无需基底膜剥脱或暴露。(摘要截选至250字)